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  • American Association for the Advancement of Science (AAAS)  (28)
  • 2010-2014  (28)
  • 1980-1984
  • 2011  (28)
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  • 2010-2014  (28)
  • 1980-1984
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  • 1
    Publication Date: 2011-02-19
    Description: Although formation and stabilization of long-lasting associative memories are thought to require time-dependent coordinated hippocampal-cortical interactions, the underlying mechanisms remain unclear. Here, we present evidence that neurons in the rat cortex must undergo a "tagging process" upon encoding to ensure the progressive hippocampal-driven rewiring of cortical networks that support remote memory storage. This process was AMPA- and N-methyl-D-aspartate receptor-dependent, information-specific, and capable of modulating remote memory persistence by affecting the temporal dynamics of hippocampal-cortical interactions. Post-learning reinforcement of the tagging process via time-limited epigenetic modifications resulted in improved remote memory retrieval. Thus, early tagging of cortical networks is a crucial neurobiological process for remote memory formation whose functional properties fit the requirements imposed by the extended time scale of systems-level memory consolidation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lesburgueres, Edith -- Gobbo, Oliviero L -- Alaux-Cantin, Stephanie -- Hambucken, Anne -- Trifilieff, Pierre -- Bontempi, Bruno -- New York, N.Y. -- Science. 2011 Feb 18;331(6019):924-8. doi: 10.1126/science.1196164.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institut des Maladies Neurodegeneratives, CNRS UMR 5293, Universites Bordeaux 1 et 2, Talence, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21330548" target="_blank"〉PubMed〈/a〉
    Keywords: Acetylation ; Animals ; Epigenesis, Genetic ; Excitatory Amino Acid Antagonists/pharmacology ; Food Preferences ; Frontal Lobe/*physiology ; Hippocampus/*physiology ; Histones/metabolism ; Learning ; Male ; *Memory, Long-Term ; Neural Pathways ; Neuronal Plasticity ; Neurons/cytology/*physiology ; Odors ; Rats ; Rats, Sprague-Dawley ; Receptors, AMPA/metabolism ; Receptors, N-Methyl-D-Aspartate/metabolism ; Reinforcement (Psychology) ; Signal Transduction ; Synapses/*physiology ; Synaptic Transmission
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2011-09-10
    Description: Engineered fluorescent protein (FP) chimeras that modulate their fluorescence in response to changes in calcium ion (Ca(2+)) concentration are powerful tools for visualizing intracellular signaling activity. However, despite a decade of availability, the palette of single FP-based Ca(2+) indicators has remained limited to a single green hue. We have expanded this palette by developing blue, improved green, and red intensiometric indicators, as well as an emission ratiometric indicator with an 11,000% ratio change. This series enables improved single-color Ca(2+) imaging in neurons and transgenic Caenorhabditis elegans. In HeLa cells, Ca(2+) was imaged in three subcellular compartments, and, in conjunction with a cyan FP-yellow FP-based indicator, Ca(2+) and adenosine 5'-triphosphate were simultaneously imaged. This palette of indicators paints the way to a colorful new era of Ca(2+) imaging.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560286/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560286/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zhao, Yongxin -- Araki, Satoko -- Wu, Jiahui -- Teramoto, Takayuki -- Chang, Yu-Fen -- Nakano, Masahiro -- Abdelfattah, Ahmed S -- Fujiwara, Manabi -- Ishihara, Takeshi -- Nagai, Takeharu -- Campbell, Robert E -- 94487/Canadian Institutes of Health Research/Canada -- 99085/Canadian Institutes of Health Research/Canada -- Canadian Institutes of Health Research/Canada -- New York, N.Y. -- Science. 2011 Sep 30;333(6051):1888-91. doi: 10.1126/science.1208592. Epub 2011 Sep 8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry, University of Alberta, Edmonton, Alberta T6G 2G2, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21903779" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine Triphosphate/metabolism ; Animals ; Animals, Genetically Modified ; Caenorhabditis elegans ; Calcium/*analysis ; *Calcium Signaling ; *Directed Molecular Evolution ; Fluorescence ; Fluorescence Resonance Energy Transfer ; Green Fluorescent Proteins/*chemistry/genetics ; HeLa Cells ; Humans ; Luminescent Proteins/*chemistry/genetics ; Molecular Sequence Data ; Neurons/metabolism ; *Protein Engineering ; Rats ; Recombinant Fusion Proteins/*chemistry ; Spectrometry, Fluorescence ; Transfection
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    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2011-11-05
    Description: Since their origin, human populations have colonized the whole planet, but the demographic processes governing range expansions are mostly unknown. We analyzed the genealogy of more than one million individuals resulting from a range expansion in Quebec between 1686 and 1960 and reconstructed the spatial dynamics of the expansion. We find that a majority of the present Saguenay Lac-Saint-Jean population can be traced back to ancestors having lived directly on or close to the wave front. Ancestors located on the front contributed significantly more to the current gene pool than those from the range core, likely due to a 20% larger effective fertility of women on the wave front. This fitness component is heritable on the wave front and not in the core, implying that this life-history trait evolves during range expansions.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Moreau, Claudia -- Bherer, Claude -- Vezina, Helene -- Jomphe, Michele -- Labuda, Damian -- Excoffier, Laurent -- New York, N.Y. -- Science. 2011 Nov 25;334(6059):1148-50. doi: 10.1126/science.1212880. Epub 2011 Nov 3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre de Recherche, Hopital Sainte-Justine, Universite de Montreal, 3175 Cote Sainte-Catherine, Montreal, Quebec, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22052972" target="_blank"〉PubMed〈/a〉
    Keywords: *Demography ; Emigration and Immigration ; Family Characteristics ; Female ; Fertility ; *Gene Pool ; Genes ; *Genetic Fitness ; Humans ; Male ; Marriage ; *Pedigree ; *Population Dynamics ; Quebec ; Registries ; Reproduction ; *Selection, Genetic
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  • 4
    Publication Date: 2011-03-26
    Description: Axon-dendrite polarization is crucial for neural network wiring and information processing in the brain. Polarization begins with the transformation of a single neurite into an axon and its subsequent rapid extension, which requires coordination of cellular energy status to allow for transport of building materials to support axon growth. We found that activation of the energy-sensing adenosine 5'-monophosphate (AMP)-activated protein kinase (AMPK) pathway suppressed axon initiation and neuronal polarization. Phosphorylation of the kinesin light chain of the Kif5 motor protein by AMPK disrupted the association of the motor with phosphatidylinositol 3-kinase (PI3K), preventing PI3K targeting to the axonal tip and inhibiting polarization and axon growth.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325765/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3325765/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Amato, Stephen -- Liu, Xiuxin -- Zheng, Bin -- Cantley, Lewis -- Rakic, Pasko -- Man, Heng-Ye -- GM41890/GM/NIGMS NIH HHS/ -- GM56203/GM/NIGMS NIH HHS/ -- K99CA133245/CA/NCI NIH HHS/ -- MH07907/MH/NIMH NIH HHS/ -- R00 CA133245/CA/NCI NIH HHS/ -- R01 GM056203/GM/NIGMS NIH HHS/ -- R01 NS014841/NS/NINDS NIH HHS/ -- R01 NS014841-32/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2011 Apr 8;332(6026):247-51. doi: 10.1126/science.1201678. Epub 2011 Mar 24.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, Boston University, 5 Cummington Street, Boston, MA 02215, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21436401" target="_blank"〉PubMed〈/a〉
    Keywords: AMP-Activated Protein Kinases/*metabolism ; Aminoimidazole Carboxamide/analogs & derivatives/pharmacology ; Animals ; Axons/enzymology/*physiology/ultrastructure ; *Cell Polarity/drug effects ; Cells, Cultured ; Hippocampus/cytology/embryology ; Metformin/pharmacology ; Mice ; Microtubule-Associated Proteins/metabolism ; Neurons/cytology/drug effects/enzymology/*physiology ; Phosphatidylinositol 3-Kinase/*metabolism ; Phosphorylation ; Proto-Oncogene Proteins c-akt/metabolism ; Rats ; Recombinant Fusion Proteins/metabolism ; Ribonucleotides/pharmacology ; Signal Transduction ; Tissue Culture Techniques
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2011-03-19
    Description: Decreased cardiac contractility is a central feature of systolic heart failure. Existing drugs increase cardiac contractility indirectly through signaling cascades but are limited by their mechanism-related adverse effects. To avoid these limitations, we previously developed omecamtiv mecarbil, a small-molecule, direct activator of cardiac myosin. Here, we show that it binds to the myosin catalytic domain and operates by an allosteric mechanism to increase the transition rate of myosin into the strongly actin-bound force-generating state. Paradoxically, it inhibits adenosine 5'-triphosphate turnover in the absence of actin, which suggests that it stabilizes an actin-bound conformation of myosin. In animal models, omecamtiv mecarbil increases cardiac function by increasing the duration of ejection without changing the rates of contraction. Cardiac myosin activation may provide a new therapeutic approach for systolic heart failure.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090309/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090309/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Malik, Fady I -- Hartman, James J -- Elias, Kathleen A -- Morgan, Bradley P -- Rodriguez, Hector -- Brejc, Katjusa -- Anderson, Robert L -- Sueoka, Sandra H -- Lee, Kenneth H -- Finer, Jeffrey T -- Sakowicz, Roman -- Baliga, Ramesh -- Cox, David R -- Garard, Marc -- Godinez, Guillermo -- Kawas, Raja -- Kraynack, Erica -- Lenzi, David -- Lu, Pu Ping -- Muci, Alexander -- Niu, Congrong -- Qian, Xiangping -- Pierce, Daniel W -- Pokrovskii, Maria -- Suehiro, Ion -- Sylvester, Sheila -- Tochimoto, Todd -- Valdez, Corey -- Wang, Wenyue -- Katori, Tatsuo -- Kass, David A -- Shen, You-Tang -- Vatner, Stephen F -- Morgans, David J -- 1-R43-HL-66647-1/HL/NHLBI NIH HHS/ -- R01 HL106511/HL/NHLBI NIH HHS/ -- R43 HL066647/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2011 Mar 18;331(6023):1439-43. doi: 10.1126/science.1200113.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Preclinical Research and Development, Cytokinetics, Inc., South San Francisco, CA 94080, USA. fmalik@cytokinetics.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21415352" target="_blank"〉PubMed〈/a〉
    Keywords: Actin Cytoskeleton/metabolism ; Actins/metabolism ; Adenosine Triphosphatases/metabolism ; Adenosine Triphosphate/metabolism ; Adrenergic beta-Agonists/pharmacology ; Allosteric Regulation ; Animals ; Binding Sites ; Calcium/metabolism ; Cardiac Myosins/chemistry/*metabolism ; Cardiac Output/drug effects ; Dogs ; Female ; Heart Failure, Systolic/*drug therapy/physiopathology ; Isoproterenol/pharmacology ; Male ; Myocardial Contraction/*drug effects ; Myocytes, Cardiac/*drug effects/physiology ; Phosphates/metabolism ; Protein Binding ; Protein Conformation ; Protein Isoforms/chemistry/metabolism ; Rats ; Rats, Sprague-Dawley ; Urea/*analogs & derivatives/chemistry/metabolism/pharmacology ; Ventricular Function, Left/drug effects
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  • 6
    Publication Date: 2011-07-09
    Description: When new learning occurs against the background of established prior knowledge, relevant new information can be assimilated into a schema and thereby expand the knowledge base. An animal model of this important component of memory consolidation reveals that systems memory consolidation can be very fast. In experiments with rats, we found that the hippocampal-dependent learning of new paired associates is associated with a striking up-regulation of immediate early genes in the prelimbic region of the medial prefrontal cortex, and that pharmacological interventions targeted at that area can prevent both new learning and the recall of remotely and even recently consolidated information. These findings challenge the concept of distinct fast (hippocampal) and slow (cortical) learning systems, and shed new light on the neural mechanisms of memory assimilation into schemas.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tse, Dorothy -- Takeuchi, Tomonori -- Kakeyama, Masaki -- Kajii, Yasushi -- Okuno, Hiroyuki -- Tohyama, Chiharu -- Bito, Haruhiko -- Morris, Richard G M -- G0700447/Medical Research Council/United Kingdom -- Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2011 Aug 12;333(6044):891-5. doi: 10.1126/science.1205274. Epub 2011 Jul 7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre for Cognitive and Neural Systems, University of Edinburgh, Edinburgh EH8 9JZ, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21737703" target="_blank"〉PubMed〈/a〉
    Keywords: 6-Cyano-7-nitroquinoxaline-2,3-dione/pharmacology ; Animals ; Cues ; Cytoskeletal Proteins/genetics ; Early Growth Response Protein 1/genetics ; *Genes, Immediate-Early ; Hippocampus/*physiology ; Learning ; Male ; *Memory ; *Mental Recall ; Neocortex/*physiology ; Nerve Tissue Proteins/genetics ; Prefrontal Cortex/*physiology ; Rats ; Receptors, AMPA/antagonists & inhibitors ; Receptors, N-Methyl-D-Aspartate/antagonists & inhibitors ; Synaptic Transmission/drug effects ; *Transcriptional Activation ; Up-Regulation
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  • 7
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2011-02-05
    Description: Once initiated near the soma, an action potential (AP) is thought to propagate autoregeneratively and distribute uniformly over axonal arbors. We challenge this classic view by showing that APs are subject to waveform modulation while they travel down axons. Using fluorescent patch-clamp pipettes, we recorded APs from axon branches of hippocampal CA3 pyramidal neurons ex vivo. The waveforms of axonal APs increased in width in response to the local application of glutamate and an adenosine A(1) receptor antagonist to the axon shafts, but not to other unrelated axon branches. Uncaging of calcium in periaxonal astrocytes caused AP broadening through ionotropic glutamate receptor activation. The broadened APs triggered larger calcium elevations in presynaptic boutons and facilitated synaptic transmission to postsynaptic neurons. This local AP modification may enable axonal computation through the geometry of axon wiring.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sasaki, Takuya -- Matsuki, Norio -- Ikegaya, Yuji -- New York, N.Y. -- Science. 2011 Feb 4;331(6017):599-601. doi: 10.1126/science.1197598.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, University of Tokyo, Tokyo 113-0033, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21292979" target="_blank"〉PubMed〈/a〉
    Keywords: *Action Potentials/drug effects ; Adenosine/metabolism/pharmacology ; Adenosine A1 Receptor Antagonists/pharmacology ; Animals ; Astrocytes/metabolism ; Axons/drug effects/*physiology ; CA3 Region, Hippocampal/*cytology/physiology ; Calcium/metabolism ; Excitatory Postsynaptic Potentials ; Glutamic Acid/pharmacology ; In Vitro Techniques ; Patch-Clamp Techniques ; Potassium Channels/metabolism ; Presynaptic Terminals/physiology ; Pyramidal Cells/*physiology ; Rats ; Rats, Wistar ; Receptor, Adenosine A1/metabolism ; Receptors, AMPA/metabolism ; *Synaptic Transmission ; Xanthines/pharmacology ; gamma-Aminobutyric Acid/pharmacology
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  • 8
    Publication Date: 2011-07-19
    Description: Reward-motivated behavior is strongly influenced by the learned significance of contextual stimuli in the environment. However, the neural pathways that mediate context-reward relations are not well understood. We have identified a circuit from area CA3 of dorsal hippocampus to ventral tegmental area (VTA) that uses lateral septum (LS) as a relay. Theta frequency stimulation of CA3 excited VTA dopamine (DA) neurons and inhibited non-DA neurons. DA neuron excitation was likely mediated by disinhibition because local antagonism of gamma-aminobutyric acid receptors blocked responses to CA3 stimulation. Inactivating components of the CA3-LS-VTA pathway blocked evoked responses in VTA and also reinstatement of cocaine-seeking by contextual stimuli. This transsynaptic link between hippocampus and VTA appears to be an important substrate by which environmental context regulates goal-directed behavior.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3150711/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3150711/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Luo, Alice H -- Tahsili-Fahadan, Pouya -- Wise, Roy A -- Lupica, Carl R -- Aston-Jones, Gary -- F31-MH071093/MH/NIMH NIH HHS/ -- R37 DA006214/DA/NIDA NIH HHS/ -- R37-DA006214/DA/NIDA NIH HHS/ -- UL1 RR029882/RR/NCRR NIH HHS/ -- ZIA DA000471-07/Intramural NIH HHS/ -- New York, N.Y. -- Science. 2011 Jul 15;333(6040):353-7. doi: 10.1126/science.1204622.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Behavioral Neuroscience Section, Behavioral Neuroscience Research Branch, National Institute on Drug Abuse Intramural Research Program, National Institutes of Health, Baltimore, MD 21224, USA. alice_luo@hotmail.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21764750" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Behavior, Animal ; Brain Mapping ; CA3 Region, Hippocampal/*physiology ; Cocaine/administration & dosage ; Dopamine/physiology ; Drug-Seeking Behavior ; Electric Stimulation ; GABA Agonists/pharmacology ; GABA Antagonists/pharmacology ; Hippocampus/physiology ; Male ; Models, Neurological ; Neural Inhibition ; Neural Pathways ; Neurons/*physiology ; Rats ; Rats, Sprague-Dawley ; *Reward ; Self Administration ; Septal Nuclei/*physiology ; Theta Rhythm ; Ventral Tegmental Area/*physiology ; gamma-Aminobutyric Acid/administration & dosage/physiology
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  • 9
    Publication Date: 2011-11-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Markram, Henry -- New York, N.Y. -- Science. 2011 Nov 11;334(6057):748-9. doi: 10.1126/science.334.6057.748.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22076354" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Brain/physiology ; *Computer Simulation ; Consciousness ; Humans ; *Models, Neurological ; Rats ; Research Support as Topic ; Software
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  • 10
    Publication Date: 2011-07-02
    Description: Central amygdala (CeA) projections to hypothalamic and brain stem nuclei regulate the behavioral and physiological expression of fear, but it is unknown whether these different aspects of the fear response can be separately regulated by the CeA. We combined fluorescent retrograde tracing of CeA projections to nuclei that modulate fear-related freezing or cardiovascular responses with in vitro electrophysiological recordings and with in vivo monitoring of related behavioral and physiological parameters. CeA projections emerged from separate neuronal populations with different electrophysiological characteristics and different response properties to oxytocin. In vivo, oxytocin decreased freezing responses in fear-conditioned rats without affecting the cardiovascular response. Thus, neuropeptidergic signaling can modulate the CeA outputs through separate neuronal circuits and thereby individually steer the various aspects of the fear response.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Viviani, Daniele -- Charlet, Alexandre -- van den Burg, Erwin -- Robinet, Camille -- Hurni, Nicolas -- Abatis, Marios -- Magara, Fulvio -- Stoop, Ron -- New York, N.Y. -- Science. 2011 Jul 1;333(6038):104-7. doi: 10.1126/science.1201043.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre for Psychiatric Neuroscience, Department of Psychiatry, Lausanne University Hospital Center, University of Lausanne, CH-1015 Lausanne, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21719680" target="_blank"〉PubMed〈/a〉
    Keywords: Amygdala/*physiology ; Animals ; Bombesin/pharmacology ; Brain Stem/*physiology ; Conditioning (Psychology) ; Fear/*physiology ; Female ; GABA-A Receptor Agonists/pharmacology ; Heart Rate/drug effects ; Hypothalamus/*physiology ; Male ; Muscimol/pharmacology ; Neural Inhibition ; Neural Pathways/physiology ; Neurons/*physiology ; Oxytocin/agonists/analogs & derivatives/pharmacology/*physiology ; Patch-Clamp Techniques ; Periaqueductal Gray/*physiology ; Rats ; Rats, Sprague-Dawley
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  • 11
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2011-12-14
    Description: Whereas human pro-social behavior is often driven by empathic concern for another, it is unclear whether nonprimate mammals experience a similar motivational state. To test for empathically motivated pro-social behavior in rodents, we placed a free rat in an arena with a cagemate trapped in a restrainer. After several sessions, the free rat learned to intentionally and quickly open the restrainer and free the cagemate. Rats did not open empty or object-containing restrainers. They freed cagemates even when social contact was prevented. When liberating a cagemate was pitted against chocolate contained within a second restrainer, rats opened both restrainers and typically shared the chocolate. Thus, rats behave pro-socially in response to a conspecific's distress, providing strong evidence for biological roots of empathically motivated helping behavior.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3760221/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3760221/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ben-Ami Bartal, Inbal -- Decety, Jean -- Mason, Peggy -- DA022429/DA/NIDA NIH HHS/ -- DA022978/DA/NIDA NIH HHS/ -- R01 DA022978/DA/NIDA NIH HHS/ -- R21 DA022429/DA/NIDA NIH HHS/ -- New York, N.Y. -- Science. 2011 Dec 9;334(6061):1427-30. doi: 10.1126/science.1210789.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, University of Chicago, Chicago, IL, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22158823" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Behavior, Animal ; Cooperative Behavior ; *Empathy ; Female ; Helping Behavior ; Male ; Motivation ; Rats ; Rats, Sprague-Dawley ; Restraint, Physical ; *Social Behavior ; *Stress, Psychological
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  • 12
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2011-04-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vogel, Gretchen -- New York, N.Y. -- Science. 2011 Apr 15;332(6027):300-1. doi: 10.1126/science.332.6027.300.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21493838" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain/cytology/growth & development/*physiology ; Embryo, Mammalian/physiology ; Embryonic Stem Cells/physiology ; *Genetic Variation ; Genome, Human ; Humans ; *Interspersed Repetitive Sequences ; Long Interspersed Nucleotide Elements/*genetics ; Methyl-CpG-Binding Protein 2/genetics ; Mice ; *Neurogenesis ; Neurons/cytology/*physiology ; Rats ; Stem Cells/cytology/*physiology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 13
    Publication Date: 2011-03-10
    Description: Memories are more easily disrupted than improved. Many agents can impair memories during encoding and consolidation. In contrast, the armamentarium of potential memory enhancers is so far rather modest. Moreover, the effect of the latter appears to be limited to enhancing new memories during encoding and the initial period of cellular consolidation, which can last from a few minutes to hours after learning. Here, we report that overexpression in the rat neocortex of the protein kinase C isozyme protein kinase Mzeta (PKMzeta) enhances long-term memory, whereas a dominant negative PKMzeta disrupts memory, even long after memory has been formed.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shema, Reut -- Haramati, Sharon -- Ron, Shiri -- Hazvi, Shoshi -- Chen, Alon -- Sacktor, Todd Charlton -- Dudai, Yadin -- MH57068/MH/NIMH NIH HHS/ -- R01 MH53576/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2011 Mar 4;331(6021):1207-10. doi: 10.1126/science.1200215.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology, Weizmann Institute of Science, Rehovot 76100, Israel.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21385716" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Conditioning (Psychology) ; Gene Expression ; Gene Transfer Techniques ; Genetic Vectors ; Isoenzymes/genetics/metabolism ; Lentivirus/genetics ; Male ; *Memory, Long-Term ; Mutant Proteins/metabolism ; Mutation ; Neocortex/*metabolism ; Neurons/metabolism ; Protein Kinase C/*genetics/*metabolism ; Rats ; Rats, Wistar
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  • 14
    Publication Date: 2011-10-25
    Description: Use-dependent forms of synaptic plasticity have been extensively characterized at chemical synapses, but a relationship between natural activity and strength at electrical synapses remains elusive. The thalamic reticular nucleus (TRN), a brain area rich in gap-junctional (electrical) synapses, regulates cortical attention to the sensory surround and participates in shifts between arousal states; plasticity of electrical synapses may be a key mechanism underlying these processes. We observed long-term depression resulting from coordinated burst firing in pairs of coupled TRN neurons. Changes in gap-junctional communication were asymmetrical, indicating that regulation of connectivity depends on the direction of use. Modification of electrical synapses resulting from activity in coupled neurons is likely to be a widespread and powerful mechanism for dynamic reorganization of electrically coupled neuronal networks.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Haas, Julie S -- Zavala, Baltazar -- Landisman, Carole E -- New York, N.Y. -- Science. 2011 Oct 21;334(6054):389-93. doi: 10.1126/science.1207502.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Children's Hospital, Department of Neurology, Harvard University, 300 Longwood Avenue, Boston, MA 02115, USA. julie.haas@gmail.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22021860" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Electrical Synapses/*physiology ; In Vitro Techniques ; Intralaminar Thalamic Nuclei/cytology/*physiology ; *Long-Term Synaptic Depression ; Membrane Potentials ; Nerve Net/physiology ; Neurons/*physiology ; Patch-Clamp Techniques ; Rats ; Rats, Sprague-Dawley ; Sodium/metabolism ; Tetrodotoxin/pharmacology
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  • 15
    Publication Date: 2011-02-05
    Description: N-glycosylation of eukaryotic proteins helps them fold and traverse the cellular secretory pathway and can increase their stability, although the molecular basis for stabilization is poorly understood. Glycosylation of proteins at naive sites (ones that normally are not glycosylated) could be useful for therapeutic and research applications but currently results in unpredictable changes to protein stability. We show that placing a phenylalanine residue two or three positions before a glycosylated asparagine in distinct reverse turns facilitates stabilizing interactions between the aromatic side chain and the first N-acetylglucosamine of the glycan. Glycosylating this portable structural module, an enhanced aromatic sequon, in three different proteins stabilizes their native states by -0.7 to -2.0 kilocalories per mole and increases cellular glycosylation efficiency.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099596/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099596/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Culyba, Elizabeth K -- Price, Joshua L -- Hanson, Sarah R -- Dhar, Apratim -- Wong, Chi-Huey -- Gruebele, Martin -- Powers, Evan T -- Kelly, Jeffery W -- AI072155/AI/NIAID NIH HHS/ -- F32 GM086039/GM/NIGMS NIH HHS/ -- F32 GM086039-03/GM/NIGMS NIH HHS/ -- GM051105/GM/NIGMS NIH HHS/ -- R01 AI072155/AI/NIAID NIH HHS/ -- R01 AI072155-04/AI/NIAID NIH HHS/ -- R01 GM051105/GM/NIGMS NIH HHS/ -- R01 GM051105-15/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2011 Feb 4;331(6017):571-5. doi: 10.1126/science.1198461.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21292975" target="_blank"〉PubMed〈/a〉
    Keywords: Acetylglucosamine/chemistry ; Acid Anhydride Hydrolases/*chemistry ; Amino Acid Sequence ; Animals ; Antigens, CD2/*chemistry ; Asparagine/chemistry ; Glycosylation ; Humans ; Models, Molecular ; Mutagenesis, Site-Directed ; Mutant Proteins/chemistry ; Peptidylprolyl Isomerase/*chemistry ; Phenylalanine/chemistry ; Polysaccharides/chemistry ; Protein Conformation ; Protein Engineering ; Protein Folding ; *Protein Stability ; Protein Structure, Tertiary ; Rats ; Thermodynamics
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  • 16
    Publication Date: 2011-01-29
    Description: Hypertrophic scarring and poor intrinsic axon growth capacity constitute major obstacles for spinal cord repair. These processes are tightly regulated by microtubule dynamics. Here, moderate microtubule stabilization decreased scar formation after spinal cord injury in rodents through various cellular mechanisms, including dampening of transforming growth factor-beta signaling. It prevented accumulation of chondroitin sulfate proteoglycans and rendered the lesion site permissive for axon regeneration of growth-competent sensory neurons. Microtubule stabilization also promoted growth of central nervous system axons of the Raphe-spinal tract and led to functional improvement. Thus, microtubule stabilization reduces fibrotic scarring and enhances the capacity of axons to grow.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3330754/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3330754/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hellal, Farida -- Hurtado, Andres -- Ruschel, Jorg -- Flynn, Kevin C -- Laskowski, Claudia J -- Umlauf, Martina -- Kapitein, Lukas C -- Strikis, Dinara -- Lemmon, Vance -- Bixby, John -- Hoogenraad, Casper C -- Bradke, Frank -- R01 HD057632/HD/NICHD NIH HHS/ -- R01 HD057632-04/HD/NICHD NIH HHS/ -- R01 NS059866/NS/NINDS NIH HHS/ -- R01 NS059866-03/NS/NINDS NIH HHS/ -- R01 NS059866-04/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2011 Feb 18;331(6019):928-31. doi: 10.1126/science.1201148. Epub 2011 Jan 27.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Axonal Growth and Regeneration Group, Max Planck Institute of Neurobiology, Martinsried, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21273450" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Axons/*physiology ; Cells, Cultured ; Chondroitin Sulfate Proteoglycans/metabolism ; Cicatrix/pathology/*prevention & control ; Female ; Ganglia, Spinal/cytology ; Kinesin/metabolism ; Microtubules/drug effects/*metabolism ; Paclitaxel/*administration & dosage/pharmacology ; Protein Transport ; Rats ; Rats, Sprague-Dawley ; Sensory Receptor Cells/physiology ; Signal Transduction ; Smad2 Protein/metabolism ; Spinal Cord/cytology/drug effects ; Spinal Cord Injuries/*drug therapy/pathology/*physiopathology ; *Spinal Cord Regeneration ; Transforming Growth Factor beta/metabolism
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  • 17
    Publication Date: 2011-12-17
    Description: Acid evokes pain by exciting nociceptors; the acid sensors are proton-gated ion channels that depolarize neurons. The naked mole-rat (Heterocephalus glaber) is exceptional in its acid insensitivity, but acid sensors (acid-sensing ion channels and the transient receptor potential vanilloid-1 ion channel) in naked mole-rat nociceptors are similar to those in other vertebrates. Acid inhibition of voltage-gated sodium currents is more profound in naked mole-rat nociceptors than in mouse nociceptors, however, which effectively prevents acid-induced action potential initiation. We describe a species-specific variant of the nociceptor sodium channel Na(V)1.7, which is potently blocked by protons and can account for acid insensitivity in this species. Thus, evolutionary pressure has selected for an Na(V)1.7 gene variant that tips the balance from proton-induced excitation to inhibition of action potential initiation to abolish acid nociception.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Smith, Ewan St John -- Omerbasic, Damir -- Lechner, Stefan G -- Anirudhan, Gireesh -- Lapatsina, Liudmila -- Lewin, Gary R -- New York, N.Y. -- Science. 2011 Dec 16;334(6062):1557-60. doi: 10.1126/science.1213760.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neuroscience, Max-Delbruck Center for Molecular Medicine, Berlin-Buch, Germany. ewan.smith@mdc-berlin.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22174253" target="_blank"〉PubMed〈/a〉
    Keywords: Acid Sensing Ion Channels ; Acids/metabolism/*pharmacology ; Action Potentials ; Amino Acid Motifs ; Animals ; Ganglia, Spinal/cytology/physiology ; Mice ; Mole Rats/genetics/*physiology ; NAV1.7 Voltage-Gated Sodium Channel ; Nerve Tissue Proteins/metabolism ; Nociception/*physiology ; Rats ; Sodium Channels/genetics/*metabolism ; TRPV Cation Channels/metabolism
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  • 18
    Publication Date: 2011-04-30
    Description: Grid cells in parahippocampal cortices fire at vertices of a periodic triangular grid that spans the entire recording environment. Such precise neural computations in space have been proposed to emerge from equally precise temporal oscillations within cells or within the local neural circuitry. We found that grid-like firing patterns in the entorhinal cortex vanished when theta oscillations were reduced after intraseptal lidocaine infusions in rats. Other spatially modulated cells in the same cortical region and place cells in the hippocampus retained their spatial firing patterns to a larger extent during these periods without well-organized oscillatory neuronal activity. Precisely timed neural activity within single cells or local networks is thus required for periodic spatial firing but not for single place fields.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koenig, Julie -- Linder, Ashley N -- Leutgeb, Jill K -- Leutgeb, Stefan -- New York, N.Y. -- Science. 2011 Apr 29;332(6029):592-5. doi: 10.1126/science.1201685.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Neurobiology Section and Center for Neural Circuits and Behavior, Division of Biological Sciences, University of California, San Diego, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21527713" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Entorhinal Cortex/cytology/*physiology ; Hippocampus/cytology/*physiology ; Lidocaine/pharmacology ; Male ; Membrane Potentials ; Motor Activity ; Nerve Net/physiology ; Neural Pathways ; Neurons/*physiology ; Periodicity ; Rats ; Rats, Long-Evans ; Septum Pellucidum/drug effects/physiology ; *Space Perception ; *Theta Rhythm/drug effects
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  • 19
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2011-09-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hidalgo, Cecilia -- Donoso, Paulina -- New York, N.Y. -- Science. 2011 Sep 9;333(6048):1388-90. doi: 10.1126/science.1212183.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Physiology and Biophysics Program, Institute of Biomedical Sciences, and Center of Molecular Studies of the Cell, Faculty of Medicine, Universidad de Chile, Santiago, Chile. chidalgo@med.uchile.cl〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21903799" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Calcium/*metabolism ; Calcium Channels/metabolism ; Calcium Signaling ; Glutathione/metabolism ; *Mechanotransduction, Cellular ; Membrane Glycoproteins/metabolism ; Mice ; Muscular Dystrophy, Animal/physiopathology ; Myocardial Contraction ; Myocytes, Cardiac/*physiology ; NADPH Oxidase/metabolism ; Oxidation-Reduction ; Rats ; Reactive Oxygen Species/*metabolism ; Ryanodine Receptor Calcium Release Channel/metabolism
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  • 20
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2011-01-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Miller, Greg -- New York, N.Y. -- Science. 2011 Jan 14;331(6014):138-40. doi: 10.1126/science.331.6014.138.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21233358" target="_blank"〉PubMed〈/a〉
    Keywords: Brain/physiology ; *Cardiovascular Physiological Phenomena ; Gene Expression Regulation ; Genes ; *Health ; Humans ; Immune System/*physiology ; Leukocytes/physiology ; *Loneliness ; *Nervous System Physiological Phenomena ; Social Isolation ; Stress, Psychological ; Surveys and Questionnaires
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  • 21
    Publication Date: 2011-10-15
    Description: During development, formation of topographic maps in sensory cortex requires precise temporal binding in thalamocortical networks. However, the physiological substrate for such synchronization is unknown. We report that early gamma oscillations (EGOs) enable precise spatiotemporal thalamocortical synchronization in the neonatal rat whisker sensory system. Driven by a thalamic gamma oscillator and initially independent of cortical inhibition, EGOs synchronize neurons in a single thalamic barreloid and corresponding cortical barrel and support plasticity at developing thalamocortical synapses. We propose that the multiple replay of sensory input in thalamocortical circuits during EGOs allows thalamic and cortical neurons to be organized into vertical topographic functional units before the development of horizontal binding in adult brain.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Minlebaev, Marat -- Colonnese, Matthew -- Tsintsadze, Timur -- Sirota, Anton -- Khazipov, Roustem -- New York, N.Y. -- Science. 2011 Oct 14;334(6053):226-9. doi: 10.1126/science.1210574.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉INSERM U901, Marseille, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21998388" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn ; Brain Waves/*physiology ; Evoked Potentials, Somatosensory ; Excitatory Postsynaptic Potentials ; Female ; Inhibitory Postsynaptic Potentials ; Interneurons ; Male ; Models, Neurological ; Nerve Net/physiology ; Neural Inhibition ; Neuronal Plasticity ; Neurons/physiology ; Patch-Clamp Techniques ; Rats ; Rats, Wistar ; Somatosensory Cortex/*growth & development/*physiology ; Synapses/physiology ; Thalamus/*growth & development/*physiology ; Vibrissae/growth & development/innervation/*physiology
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  • 22
    Publication Date: 2011-10-29
    Description: Abeta (beta-amyloid peptide) is an important contributor to Alzheimer's disease (AD). We modeled Abeta toxicity in yeast by directing the peptide to the secretory pathway. A genome-wide screen for toxicity modifiers identified the yeast homolog of phosphatidylinositol binding clathrin assembly protein (PICALM) and other endocytic factors connected to AD whose relationship to Abeta was previously unknown. The factors identified in yeast modified Abeta toxicity in glutamatergic neurons of Caenorhabditis elegans and in primary rat cortical neurons. In yeast, Abeta impaired the endocytic trafficking of a plasma membrane receptor, which was ameliorated by endocytic pathway factors identified in the yeast screen. Thus, links between Abeta, endocytosis, and human AD risk factors can be ascertained with yeast as a model system.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281757/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281757/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Treusch, Sebastian -- Hamamichi, Shusei -- Goodman, Jessica L -- Matlack, Kent E S -- Chung, Chee Yeun -- Baru, Valeriya -- Shulman, Joshua M -- Parrado, Antonio -- Bevis, Brooke J -- Valastyan, Julie S -- Han, Haesun -- Lindhagen-Persson, Malin -- Reiman, Eric M -- Evans, Denis A -- Bennett, David A -- Olofsson, Anders -- DeJager, Philip L -- Tanzi, Rudolph E -- Caldwell, Kim A -- Caldwell, Guy A -- Lindquist, Susan -- F32 NS067782-02/NS/NINDS NIH HHS/ -- K08 AG034290/AG/NIA NIH HHS/ -- K08AG034290/AG/NIA NIH HHS/ -- P30 AG019610/AG/NIA NIH HHS/ -- P30AG10161/AG/NIA NIH HHS/ -- R01 AG015819/AG/NIA NIH HHS/ -- R01 AG017917/AG/NIA NIH HHS/ -- R01AG15819/AG/NIA NIH HHS/ -- R01AG17917/AG/NIA NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2011 Dec 2;334(6060):1241-5. doi: 10.1126/science.1213210. Epub 2011 Oct 27.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22033521" target="_blank"〉PubMed〈/a〉
    Keywords: Alzheimer Disease/*genetics/*metabolism ; Amyloid beta-Peptides/chemistry/genetics/*metabolism ; Animals ; Animals, Genetically Modified ; Caenorhabditis elegans/cytology/genetics/metabolism ; Cell Membrane/metabolism ; Cells, Cultured ; Clathrin/metabolism ; Cytoskeleton/metabolism ; Disease Susceptibility ; *Endocytosis ; Genetic Association Studies ; Genetic Testing ; Glutamates/metabolism ; Humans ; Monomeric Clathrin Assembly Proteins/genetics/metabolism ; Neurons/physiology ; Peptide Fragments/chemistry/genetics/*metabolism ; Protein Multimerization ; Protein Transport ; Rats ; Risk Factors ; *Saccharomyces cerevisiae/cytology/genetics/growth & development/metabolism ; Saccharomyces cerevisiae Proteins/genetics/metabolism ; Secretory Pathway
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  • 23
    Publication Date: 2011-02-05
    Description: We describe the draft genome of the microcrustacean Daphnia pulex, which is only 200 megabases and contains at least 30,907 genes. The high gene count is a consequence of an elevated rate of gene duplication resulting in tandem gene clusters. More than a third of Daphnia's genes have no detectable homologs in any other available proteome, and the most amplified gene families are specific to the Daphnia lineage. The coexpansion of gene families interacting within metabolic pathways suggests that the maintenance of duplicated genes is not random, and the analysis of gene expression under different environmental conditions reveals that numerous paralogs acquire divergent expression patterns soon after duplication. Daphnia-specific genes, including many additional loci within sequenced regions that are otherwise devoid of annotations, are the most responsive genes to ecological challenges.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3529199/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3529199/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Colbourne, John K -- Pfrender, Michael E -- Gilbert, Donald -- Thomas, W Kelley -- Tucker, Abraham -- Oakley, Todd H -- Tokishita, Shinichi -- Aerts, Andrea -- Arnold, Georg J -- Basu, Malay Kumar -- Bauer, Darren J -- Caceres, Carla E -- Carmel, Liran -- Casola, Claudio -- Choi, Jeong-Hyeon -- Detter, John C -- Dong, Qunfeng -- Dusheyko, Serge -- Eads, Brian D -- Frohlich, Thomas -- Geiler-Samerotte, Kerry A -- Gerlach, Daniel -- Hatcher, Phil -- Jogdeo, Sanjuro -- Krijgsveld, Jeroen -- Kriventseva, Evgenia V -- Kultz, Dietmar -- Laforsch, Christian -- Lindquist, Erika -- Lopez, Jacqueline -- Manak, J Robert -- Muller, Jean -- Pangilinan, Jasmyn -- Patwardhan, Rupali P -- Pitluck, Samuel -- Pritham, Ellen J -- Rechtsteiner, Andreas -- Rho, Mina -- Rogozin, Igor B -- Sakarya, Onur -- Salamov, Asaf -- Schaack, Sarah -- Shapiro, Harris -- Shiga, Yasuhiro -- Skalitzky, Courtney -- Smith, Zachary -- Souvorov, Alexander -- Sung, Way -- Tang, Zuojian -- Tsuchiya, Dai -- Tu, Hank -- Vos, Harmjan -- Wang, Mei -- Wolf, Yuri I -- Yamagata, Hideo -- Yamada, Takuji -- Ye, Yuzhen -- Shaw, Joseph R -- Andrews, Justen -- Crease, Teresa J -- Tang, Haixu -- Lucas, Susan M -- Robertson, Hugh M -- Bork, Peer -- Koonin, Eugene V -- Zdobnov, Evgeny M -- Grigoriev, Igor V -- Lynch, Michael -- Boore, Jeffrey L -- P42 ES004699/ES/NIEHS NIH HHS/ -- P42 ES004699-25/ES/NIEHS NIH HHS/ -- P42ES004699/ES/NIEHS NIH HHS/ -- R01 ES019324/ES/NIEHS NIH HHS/ -- R24 GM078274/GM/NIGMS NIH HHS/ -- R24 GM078274-01A1/GM/NIGMS NIH HHS/ -- R24GM07827401/GM/NIGMS NIH HHS/ -- Intramural NIH HHS/ -- New York, N.Y. -- Science. 2011 Feb 4;331(6017):555-61. doi: 10.1126/science.1197761.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Genomics and Bioinformatics, Indiana University, 915 East Third Street, Bloomington, IN 47405, USA. jcolbour@indiana.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21292972" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptation, Physiological ; Amino Acid Sequence ; Animals ; Base Sequence ; Chromosome Mapping ; Daphnia/*genetics/physiology ; *Ecosystem ; Environment ; Evolution, Molecular ; Gene Conversion ; Gene Duplication ; Gene Expression ; Gene Expression Profiling ; Gene Expression Regulation ; Genes ; Genes, Duplicate ; *Genome ; Metabolic Networks and Pathways/genetics ; Molecular Sequence Annotation ; Molecular Sequence Data ; Multigene Family ; Phylogeny ; Sequence Analysis, DNA
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  • 24
    Publication Date: 2011-09-10
    Description: We report that in heart cells, physiologic stretch rapidly activates reduced-form nicotinamide adenine dinucleotide phosphate (NADPH) oxidase 2 (NOX2) to produce reactive oxygen species (ROS) in a process dependent on microtubules (X-ROS signaling). ROS production occurs in the sarcolemmal and t-tubule membranes where NOX2 is located and sensitizes nearby ryanodine receptors (RyRs) in the sarcoplasmic reticulum (SR). This triggers a burst of Ca(2+) sparks, the elementary Ca(2+) release events in heart. Although this stretch-dependent "tuning" of RyRs increases Ca(2+) signaling sensitivity in healthy cardiomyocytes, in disease it enables Ca(2+) sparks to trigger arrhythmogenic Ca(2+) waves. In the mouse model of Duchenne muscular dystrophy, hyperactive X-ROS signaling contributes to cardiomyopathy through aberrant Ca(2+) release from the SR. X-ROS signaling thus provides a mechanistic explanation for the mechanotransduction of Ca(2+) release in the heart and offers fresh therapeutic possibilities.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Prosser, Benjamin L -- Ward, Christopher W -- Lederer, W J -- L40 AR056534/AR/NIAMS NIH HHS/ -- P01 HL67849/HL/NHLBI NIH HHS/ -- R01 HL106059/HL/NHLBI NIH HHS/ -- R01 HL36974/HL/NHLBI NIH HHS/ -- RC2 NR011968/NR/NINR NIH HHS/ -- S10 RR023028/RR/NCRR NIH HHS/ -- T32 HL072751-07/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2011 Sep 9;333(6048):1440-5. doi: 10.1126/science.1202768.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Biomedical Engineering and Technology (BioMET), University of Maryland School of Medicine, Baltimore, MD 21209, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21903813" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Calcium/metabolism ; Calcium Signaling ; Electric Stimulation ; *Mechanotransduction, Cellular ; Membrane Glycoproteins/antagonists & inhibitors/*metabolism ; Mice ; Mice, Inbred C57BL ; Mice, Inbred mdx ; Microtubules/metabolism ; Muscular Dystrophy, Animal/metabolism/physiopathology ; Myocardial Contraction ; Myocytes, Cardiac/metabolism/*physiology ; NADPH Oxidase/antagonists & inhibitors/*metabolism ; Oxidation-Reduction ; Rats ; Rats, Sprague-Dawley ; Reactive Oxygen Species/*metabolism ; Ryanodine Receptor Calcium Release Channel/metabolism ; Sarcolemma/metabolism ; Sarcoplasmic Reticulum/metabolism ; Signal Transduction
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 25
    Publication Date: 2011-01-08
    Description: The role of electrical synapses in synchronizing neuronal assemblies in the adult mammalian brain is well documented. However, their role in learning and memory processes remains unclear. By combining Pavlovian fear conditioning, activity-dependent immediate early gene expression, and in vivo electrophysiology, we discovered that blocking neuronal gap junctions within the dorsal hippocampus impaired context-dependent fear learning, memory, and extinction. Theta rhythms in freely moving rats were also disrupted. Our results show that gap junction-mediated neuronal transmission is a prominent feature underlying emotional memories.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276370/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276370/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bissiere, Stephanie -- Zelikowsky, Moriel -- Ponnusamy, Ravikumar -- Jacobs, Nathan S -- Blair, Hugh T -- Fanselow, Michael S -- P01 NS035985/NS/NINDS NIH HHS/ -- P01NS35985/NS/NINDS NIH HHS/ -- R01 MH062122/MH/NIMH NIH HHS/ -- R01 MH079511/MH/NIMH NIH HHS/ -- R01-MH079511/MH/NIMH NIH HHS/ -- R01-MH62122/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2011 Jan 7;331(6013):87-91. doi: 10.1126/science.1193785.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, University of California, Los Angeles, CA 90095, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21212357" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Carbenoxolone/pharmacology ; Conditioning, Classical ; Connexins/antagonists & inhibitors/metabolism ; Electrical Synapses/drug effects/*physiology ; Extinction, Psychological ; *Fear ; Gene Expression/drug effects ; Genes, fos ; Hippocampus/*physiology ; *Learning ; Male ; Mefloquine/pharmacology ; *Memory ; Rats ; Rats, Long-Evans ; Theta Rhythm
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 26
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2011-02-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Botstein, David -- New York, N.Y. -- Science. 2011 Feb 25;331(6020):1025. doi: 10.1126/science.1204038.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21350164" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Evolution ; Genes ; *Human Genome Project/economics ; Humans ; Proteins/genetics/physiology ; *Sequence Analysis, DNA/economics
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 27
    Publication Date: 2011-11-19
    Description: How rudimentary movements evolve into sophisticated ones during development remains unclear. It is often assumed that the primitive patterns of neural control are suppressed during development, replaced by entirely new patterns. Here we identified the basic patterns of lumbosacral motoneuron activity from multimuscle recordings in stepping neonates, toddlers, preschoolers, and adults. Surprisingly, we found that the two basic patterns of stepping neonates are retained through development, augmented by two new patterns first revealed in toddlers. Markedly similar patterns were observed also in the rat, cat, macaque, and guineafowl, consistent with the hypothesis that, despite substantial phylogenetic distances and morphological differences, locomotion in several animal species is built starting from common primitives, perhaps related to a common ancestral neural network.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dominici, Nadia -- Ivanenko, Yuri P -- Cappellini, Germana -- d'Avella, Andrea -- Mondi, Vito -- Cicchese, Marika -- Fabiano, Adele -- Silei, Tiziana -- Di Paolo, Ambrogio -- Giannini, Carlo -- Poppele, Richard E -- Lacquaniti, Francesco -- New York, N.Y. -- Science. 2011 Nov 18;334(6058):997-9. doi: 10.1126/science.1210617.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Neuromotor Physiology, IRCCS Santa Lucia Foundation, Rome, Italy.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22096202" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Biological Evolution ; Biomechanical Phenomena ; Cats ; Child, Preschool ; Electromyography ; Humans ; Infant ; Infant, Newborn ; Leg/*physiology ; *Locomotion ; Macaca mulatta ; *Motor Activity ; Motor Neurons/*physiology ; Muscle, Skeletal/innervation/*physiology ; Nerve Net/physiology ; Rats ; Spinal Cord/physiology ; *Walking
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 28
    Publication Date: 2011-04-30
    Description: Grid cells recorded in the medial entorhinal cortex of freely moving rats exhibit firing at regular spatial locations and temporal modulation with theta rhythm oscillations (4 to 11 hertz). We analyzed grid cell spatial coding during reduction of network theta rhythm oscillations caused by medial septum (MS) inactivation with muscimol. During MS inactivation, grid cells lost their spatial periodicity, whereas head-direction cells maintained their selectivity. Conjunctive grid-by-head-direction cells lost grid cell spatial periodicity but retained head-direction specificity. All cells showed reduced rhythmicity in autocorrelations and cross-correlations. This supports the hypothesis that spatial coding by grid cells requires theta oscillations, and dissociates the mechanisms underlying the generation of entorhinal grid cell periodicity and head-direction selectivity.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3252766/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3252766/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brandon, Mark P -- Bogaard, Andrew R -- Libby, Christopher P -- Connerney, Michael A -- Gupta, Kishan -- Hasselmo, Michael E -- MH61492/MH/NIMH NIH HHS/ -- R01 MH060013/MH/NIMH NIH HHS/ -- R01 MH060013-11A1/MH/NIMH NIH HHS/ -- R01 MH060013-12/MH/NIMH NIH HHS/ -- R01 MH060013-13/MH/NIMH NIH HHS/ -- R01 MH061492/MH/NIMH NIH HHS/ -- R01 MH061492-09/MH/NIMH NIH HHS/ -- R01 MH061492-10/MH/NIMH NIH HHS/ -- R01 MH60013/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2011 Apr 29;332(6029):595-9. doi: 10.1126/science.1201652.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Memory and Brain, Department of Psychology, Graduate Program for Neuroscience, Boston University, 2 Cummington Street, Boston, MA 02215, USA. markpb68@bu.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21527714" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Entorhinal Cortex/cytology/*physiology ; Male ; Membrane Potentials ; Motor Activity ; Muscimol/pharmacology ; Nerve Net/physiology ; Neural Pathways ; Neurons/*physiology ; Periodicity ; Rats ; Rats, Long-Evans ; Septum Pellucidum/drug effects/physiology ; *Space Perception ; *Theta Rhythm/drug effects
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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