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  • 1
    Publication Date: 1998-09-11
    Description: Hypertrophic cardiomyopathy (HCM) is an inherited form of heart disease that affects 1 in 500 individuals. Here it is shown that calcineurin, a calcium-regulated phosphatase, plays a critical role in the pathogenesis of HCM. Administration of the calcineurin inhibitors cyclosporin and FK506 prevented disease in mice that were genetically predisposed to develop HCM as a result of aberrant expression of tropomodulin, myosin light chain-2, or fetal beta-tropomyosin in the heart. Cyclosporin had a similar effect in a rat model of pressure-overload hypertrophy. These results suggest that calcineurin inhibitors merit investigation as potential therapeutics for certain forms of human heart disease.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sussman, M A -- Lim, H W -- Gude, N -- Taigen, T -- Olson, E N -- Robbins, J -- Colbert, M C -- Gualberto, A -- Wieczorek, D F -- Molkentin, J D -- HL58224-01/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1998 Sep 11;281(5383):1690-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Molecular Cardiovascular Biology, Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9733519" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Calcineurin/metabolism ; *Calcineurin Inhibitors ; Calcium/metabolism ; *Cardiac Myosins ; Cardiomegaly/metabolism/pathology/*prevention & control ; Cardiomyopathy, Dilated/pathology/*prevention & control ; Cardiomyopathy, Hypertrophic/genetics/metabolism/pathology/*prevention & control ; Carrier Proteins/genetics ; Cyclosporine/*pharmacology ; Female ; Mice ; Mice, Transgenic ; *Microfilament Proteins ; Models, Cardiovascular ; Myocardium/*metabolism/pathology ; Myosin Light Chains/genetics/metabolism ; Rats ; Signal Transduction ; Tacrolimus/*pharmacology ; Tropomodulin ; Tropomyosin/genetics
    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
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2001-03-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Olson, E N -- New York, N.Y. -- Science. 2001 Mar 23;291(5512):2327-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA. eolson@hamon.swmed.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11269304" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Blood Cells ; Bone Morphogenetic Proteins/metabolism ; Calcium-Calmodulin-Dependent Protein Kinases/metabolism ; Central Nervous System/embryology/metabolism ; Cytoskeletal Proteins/metabolism ; Drosophila/embryology/metabolism ; *Drosophila Proteins ; *Embryonic Induction ; Endoderm/physiology ; Gene Expression Regulation, Developmental ; Glycogen Synthase Kinase 3 ; Heart/*embryology ; Hematopoiesis ; Insect Proteins/metabolism ; Intercellular Signaling Peptides and Proteins ; Mesoderm/cytology/physiology ; Notochord/metabolism ; Phosphorylation ; Proteins/*metabolism ; Signal Transduction ; *Trans-Activators ; Transcription Factors/metabolism ; Vertebrates/embryology ; Wnt Proteins ; Wnt3 Protein ; *Xenopus Proteins ; Zebrafish Proteins ; beta Catenin
    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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  • 3
    Publication Date: 2009-09-04
    Description: The emergence of terrestrial life witnessed the need for more sophisticated circulatory systems. This has evolved in birds, mammals and crocodilians into complete septation of the heart into left and right sides, allowing separate pulmonary and systemic circulatory systems, a key requirement for the evolution of endothermy. However, the evolution of the amniote heart is poorly understood. Reptilian hearts have been the subject of debate in the context of the evolution of cardiac septation: do they possess a single ventricular chamber or two incompletely septated ventricles? Here we examine heart development in the red-eared slider turtle, Trachemys scripta elegans (a chelonian), and the green anole, Anolis carolinensis (a squamate), focusing on gene expression in the developing ventricles. Both reptiles initially form a ventricular chamber that homogenously expresses the T-box transcription factor gene Tbx5. In contrast, in birds and mammals, Tbx5 is restricted to left ventricle precursors. In later stages, Tbx5 expression in the turtle (but not anole) heart is gradually restricted to a distinct left ventricle, forming a left-right gradient. This suggests that Tbx5 expression was refined during evolution to pattern the ventricles. In support of this hypothesis, we show that loss of Tbx5 in the mouse ventricle results in a single chamber lacking distinct identity, indicating a requirement for Tbx5 in septation. Importantly, misexpression of Tbx5 throughout the developing myocardium to mimic the reptilian expression pattern also results in a single mispatterned ventricular chamber lacking septation. Thus ventricular septation is established by a steep and correctly positioned Tbx5 gradient. Our findings provide a molecular mechanism for the evolution of the amniote ventricle, and support the concept that altered expression of developmental regulators is a key mechanism of vertebrate evolution.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2753965/" 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/PMC2753965/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koshiba-Takeuchi, Kazuko -- Mori, Alessandro D -- Kaynak, Bogac L -- Cebra-Thomas, Judith -- Sukonnik, Tatyana -- Georges, Romain O -- Latham, Stephany -- Beck, Laurel -- Henkelman, R Mark -- Black, Brian L -- Olson, Eric N -- Wade, Juli -- Takeuchi, Jun K -- Nemer, Mona -- Gilbert, Scott F -- Bruneau, Benoit G -- C06 RR018928/RR/NCRR NIH HHS/ -- P01 HL089707/HL/NHLBI NIH HHS/ -- P01 HL089707-01A1/HL/NHLBI NIH HHS/ -- P01HL089707/HL/NHLBI NIH HHS/ -- R01 HL064658/HL/NHLBI NIH HHS/ -- England -- Nature. 2009 Sep 3;461(7260):95-8. doi: 10.1038/nature08324.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Gladstone Institute of Cardiovascular Disease, San Francisco, California 94158, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19727199" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chick Embryo ; *Evolution, Molecular ; Gene Expression Regulation, Developmental ; Heart/anatomy & histology/*embryology ; Lizards/anatomy & histology/*embryology/genetics ; Mice ; Organogenesis ; T-Box Domain Proteins/deficiency/genetics/metabolism ; Turtles/anatomy & histology/*embryology/genetics
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2006-07-22
    Description: The early morphogenetic mechanisms involved in heart formation are evolutionarily conserved. A screen for genes that control Drosophila heart development revealed a cardiac defect in which pericardial and cardial cells dissociate, which causes loss of cardiac function and embryonic lethality. This phenotype resulted from mutations in the genes encoding HMG-CoA reductase, downstream enzymes in the mevalonate pathway, and G protein Ggamma1, which is geranylgeranylated, thus representing an end point of isoprenoid biosynthesis. Our findings reveal a cardial cell-autonomous requirement of Ggamma1 geranylgeranylation for heart formation and suggest the involvement of the mevalonate pathway in congenital heart disease.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yi, Peng -- Han, Zhe -- Li, Xiumin -- Olson, Eric N -- New York, N.Y. -- Science. 2006 Sep 1;313(5791):1301-3. Epub 2006 Jul 20.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, University of Texas Southwestern Medical Center, 6000 Harry Hines Boulevard, Dallas, TX 75390-9148, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16857902" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Motifs ; Animals ; Animals, Genetically Modified ; Cell Adhesion ; Drosophila melanogaster/*embryology/genetics/metabolism ; Embryo, Nonmammalian/metabolism ; GTP-Binding Proteins/chemistry/genetics/*metabolism ; Heart/*embryology ; Heart Defects, Congenital/etiology ; Hydroxymethylglutaryl CoA Reductases/genetics/metabolism ; Hydroxymethylglutaryl-CoA Reductase Inhibitors/pharmacology ; Mevalonic Acid/*metabolism ; Models, Animal ; Mutation ; Myocardium/cytology/metabolism ; Pericardium/cytology ; Protein Prenylation ; Transgenes
    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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  • 5
    Publication Date: 2011-02-26
    Description: Certain fish and amphibians retain a robust capacity for cardiac regeneration throughout life, but the same is not true of the adult mammalian heart. Whether the capacity for cardiac regeneration is absent in mammals or whether it exists and is switched off early after birth has been unclear. We found that the hearts of 1-day-old neonatal mice can regenerate after partial surgical resection, but this capacity is lost by 7 days of age. This regenerative response in 1-day-old mice was characterized by cardiomyocyte proliferation with minimal hypertrophy or fibrosis, thereby distinguishing it from repair processes. Genetic fate mapping indicated that the majority of cardiomyocytes within the regenerated tissue originated from preexisting cardiomyocytes. Echocardiography performed 2 months after surgery revealed that the regenerated ventricular apex had normal systolic function. Thus, for a brief period after birth, the mammalian heart appears to have the capacity to regenerate.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099478/" 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/PMC3099478/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Porrello, Enzo R -- Mahmoud, Ahmed I -- Simpson, Emma -- Hill, Joseph A -- Richardson, James A -- Olson, Eric N -- Sadek, Hesham A -- HL100401-01/HL/NHLBI NIH HHS/ -- R01 HL077439/HL/NHLBI NIH HHS/ -- R01 HL077439-06/HL/NHLBI NIH HHS/ -- R01 HL077439-06W1/HL/NHLBI NIH HHS/ -- R01 HL077439-07/HL/NHLBI NIH HHS/ -- R01 HL077439-08/HL/NHLBI NIH HHS/ -- R01 HL093039/HL/NHLBI NIH HHS/ -- R01 HL093039-01A1/HL/NHLBI NIH HHS/ -- R01 HL093039-01A1W1/HL/NHLBI NIH HHS/ -- R01 HL093039-02/HL/NHLBI NIH HHS/ -- R01 HL093039-03/HL/NHLBI NIH HHS/ -- R01 HL115275/HL/NHLBI NIH HHS/ -- R37 HL053351/HL/NHLBI NIH HHS/ -- R37 HL053351-12/HL/NHLBI NIH HHS/ -- R37 HL053351-13/HL/NHLBI NIH HHS/ -- R37 HL053351-14/HL/NHLBI NIH HHS/ -- R37 HL053351-15/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2011 Feb 25;331(6020):1078-80. doi: 10.1126/science.1200708.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21350179" target="_blank"〉PubMed〈/a〉
    Keywords: Aging ; Animals ; Animals, Newborn ; Cardiomegaly ; Cell Lineage ; Cell Proliferation ; Echocardiography ; Fibrosis ; Heart/*physiology ; Heart Ventricles/surgery ; Mice ; Myocardial Contraction ; Myocardium/pathology ; Myocytes, Cardiac/*physiology ; *Regeneration ; Sarcomeres/ultrastructure ; Stroke Volume
    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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  • 6
    Publication Date: 1997-05-30
    Description: Members of the myocyte enhancer factor-2 (MEF2) family of MADS (MCM1, agamous, deficiens, serum response factor)-box transcription factors bind an A-T-rich DNA sequence associated with muscle-specific genes. The murine MEF2C gene is expressed in heart precursor cells before formation of the linear heart tube. In mice homozygous for a null mutation of MEF2C, the heart tube did not undergo looping morphogenesis, the future right ventricle did not form, and a subset of cardiac muscle genes was not expressed. The absence of the right ventricular region of the mutant heart correlated with down-regulation of the dHAND gene, which encodes a basic helix-loop-helix transcription factor required for cardiac morphogenesis. Thus, MEF2C is an essential regulator of cardiac myogenesis and right ventricular development.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437729/" 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/PMC4437729/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lin, Q -- Schwarz, J -- Bucana, C -- Olson, E N -- R01 HL053351/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1997 May 30;276(5317):1404-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology and Oncology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75235-9148, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9162005" target="_blank"〉PubMed〈/a〉
    Keywords: Acyltransferases/metabolism ; Animals ; Gene Expression Regulation, Developmental ; Gene Targeting ; Heart/*embryology ; Heart Ventricles/cytology/embryology ; In Situ Hybridization ; MEF2 Transcription Factors ; Mice ; Mice, Inbred C57BL ; *Morphogenesis/genetics/physiology ; Mutagenesis ; Myocardium/cytology ; Myogenic Regulatory Factors/genetics/*physiology ; Stem Cells
    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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  • 7
    Publication Date: 2002-12-21
    Description: Members of the MyoD family of basic helix-loop-helix (bHLH) transcription factors control the formation of all skeletal muscles in vertebrates, but little is known of the molecules or mechanisms that confer unique identities to different types of skeletal muscles. MyoR and capsulin are related bHLH transcription factors expressed in specific facial muscle precursors. We show that specific facial muscles are missing in mice lacking both MyoR and capsulin, reflecting the absence of MyoD family gene expression and ablation of the corresponding myogenic lineages. These findings identify MyoR and capsulin as unique transcription factors for the development of specific head muscles.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lu, Jian-Rong -- Bassel-Duby, Rhonda -- Hawkins, April -- Chang, Priscilla -- Valdez, Renee -- Wu, Hai -- Gan, Lin -- Shelton, John M -- Richardson, James A -- Olson, Eric N -- New York, N.Y. -- Science. 2002 Dec 20;298(5602):2378-81.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, University of Texas Southwestern Medical Center at Dallas, 6000 Harry Hines Boulevard, Dallas, TX 75390-9148, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/12493912" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apoptosis ; Basic Helix-Loop-Helix Transcription Factors ; Branchial Region/embryology/metabolism ; Cell Lineage ; Cleft Palate/embryology ; Crosses, Genetic ; *DNA-Binding Proteins ; Facial Muscles/cytology/*embryology/growth & development ; Female ; Gene Expression Regulation, Developmental ; Gene Targeting ; Head ; Helix-Loop-Helix Motifs ; Hernia, Diaphragmatic/embryology ; Homozygote ; In Situ Nick-End Labeling ; Male ; Masticatory Muscles/cytology/*embryology/growth & development ; Mice ; Muscle Cells/cytology/physiology ; *Muscle Development ; Muscle Proteins/genetics/metabolism ; Muscle, Skeletal/embryology ; Mutation ; MyoD Protein/genetics/metabolism ; Myogenic Regulatory Factor 5 ; Phenotype ; *Trans-Activators ; Transcription Factors/genetics/*physiology
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 8
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-04-16
    Description: Cell-cell fusion is fundamental to the development and physiology of multicellular organisms, but little is known of its mechanistic underpinnings. Recent studies have revealed that many proteins involved in cell-cell fusion are also required for seemingly unrelated cellular processes such as phagocytosis, cell migration, axon growth, and synaptogenesis. We review advances in understanding cell-cell fusion by contrasting it with virus-cell and intracellular vesicle fusion. We also consider how proteins involved in general aspects of membrane dynamics have been co-opted to control fusion of diverse cell types by coupling with specialized proteins involved in cell-cell recognition, adhesion, and signaling.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chen, Elizabeth H -- Olson, Eric N -- New York, N.Y. -- Science. 2005 Apr 15;308(5720):369-73.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. echen@jhmi.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15831748" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Cell Fusion ; Cytoplasmic Vesicles/physiology ; Cytoskeleton/physiology ; Disease ; Humans ; Membrane Fusion ; Membrane Proteins/physiology ; Models, Biological ; Signal Transduction ; Therapeutics ; Viral Fusion Proteins/metabolism ; Virus Physiological Phenomena
    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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  • 9
    Publication Date: 2011-01-21
    Description: First recognized as regulators of development in worms and fruitflies, microRNAs are emerging as pivotal modulators of mammalian cardiovascular development and disease. Individual microRNAs modulate the expression of collections of messenger RNA targets that often have related functions, thereby governing complex biological processes. The wideranging functions of microRNAs in the cardiovascular system have provided new perspectives on disease mechanisms and have revealed intriguing therapeutic targets, as well as diagnostics, for a variety of cardiovascular disorders.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3073349/" 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/PMC3073349/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Small, Eric M -- Olson, Eric N -- R01 HL077439/HL/NHLBI NIH HHS/ -- R01 HL077439-01/HL/NHLBI NIH HHS/ -- R01 HL077439-02/HL/NHLBI NIH HHS/ -- R01 HL077439-03/HL/NHLBI NIH HHS/ -- R01 HL077439-04/HL/NHLBI NIH HHS/ -- R01 HL077439-05/HL/NHLBI NIH HHS/ -- R01 HL077439-06/HL/NHLBI NIH HHS/ -- R01 HL077439-06W1/HL/NHLBI NIH HHS/ -- R01 HL077439-07/HL/NHLBI NIH HHS/ -- R01 HL077439-08/HL/NHLBI NIH HHS/ -- R01 HL093039/HL/NHLBI NIH HHS/ -- R01 HL093039-01A1/HL/NHLBI NIH HHS/ -- R01 HL093039-01A1W1/HL/NHLBI NIH HHS/ -- R01 HL093039-02/HL/NHLBI NIH HHS/ -- R01 HL093039-03/HL/NHLBI NIH HHS/ -- R37 HL053351/HL/NHLBI NIH HHS/ -- R37 HL053351-09/HL/NHLBI NIH HHS/ -- R37 HL053351-09S1/HL/NHLBI NIH HHS/ -- R37 HL053351-10/HL/NHLBI NIH HHS/ -- R37 HL053351-11/HL/NHLBI NIH HHS/ -- R37 HL053351-12/HL/NHLBI NIH HHS/ -- R37 HL053351-13/HL/NHLBI NIH HHS/ -- R37 HL053351-14/HL/NHLBI NIH HHS/ -- R37 HL053351-15/HL/NHLBI NIH HHS/ -- England -- Nature. 2011 Jan 20;469(7330):336-42. doi: 10.1038/nature09783.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, Texas 75390-9148, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21248840" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blood Vessels/growth & development/metabolism ; Cardiovascular Diseases/diagnosis/*genetics/*therapy ; Cardiovascular System/embryology/growth & development/*metabolism ; Humans ; MicroRNAs/antagonists & inhibitors/*genetics/*metabolism ; Mutation
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 10
    Publication Date: 2012-06-05
    Description: The adult mammalian heart possesses little regenerative potential following injury. Fibrosis due to activation of cardiac fibroblasts impedes cardiac regeneration and contributes to loss of contractile function, pathological remodelling and susceptibility to arrhythmias. Cardiac fibroblasts account for a majority of cells in the heart and represent a potential cellular source for restoration of cardiac function following injury through phenotypic reprogramming to a myocardial cell fate. Here we show that four transcription factors, GATA4, HAND2, MEF2C and TBX5, can cooperatively reprogram adult mouse tail-tip and cardiac fibroblasts into beating cardiac-like myocytes in vitro. Forced expression of these factors in dividing non-cardiomyocytes in mice reprograms these cells into functional cardiac-like myocytes, improves cardiac function and reduces adverse ventricular remodelling following myocardial infarction. Our results suggest a strategy for cardiac repair through reprogramming fibroblasts resident in the heart with cardiogenic transcription factors or other molecules.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3367390/" 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/PMC3367390/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Song, Kunhua -- Nam, Young-Jae -- Luo, Xiang -- Qi, Xiaoxia -- Tan, Wei -- Huang, Guo N -- Acharya, Asha -- Smith, Christopher L -- Tallquist, Michelle D -- Neilson, Eric G -- Hill, Joseph A -- Bassel-Duby, Rhonda -- Olson, Eric N -- K99 HL114738/HL/NHLBI NIH HHS/ -- P50 HL061033/HL/NHLBI NIH HHS/ -- R01 AR040339/AR/NIAMS NIH HHS/ -- R01 HL053351/HL/NHLBI NIH HHS/ -- R01 HL061544/HL/NHLBI NIH HHS/ -- R01 HL077439/HL/NHLBI NIH HHS/ -- R01 HL083371/HL/NHLBI NIH HHS/ -- R01 HL093039/HL/NHLBI NIH HHS/ -- R01 HL111665/HL/NHLBI NIH HHS/ -- R37 HL053351/HL/NHLBI NIH HHS/ -- S10 RR019137/RR/NCRR NIH HHS/ -- England -- Nature. 2012 May 13;485(7400):599-604. doi: 10.1038/nature11139.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, Texas 75390-9148, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22660318" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Basic Helix-Loop-Helix Transcription Factors/genetics/metabolism ; Cell Lineage ; *Cell Transdifferentiation ; *Cellular Reprogramming ; Fibroblasts/*cytology/physiology ; Heart/*physiology/physiopathology ; Mice ; Myocardial Infarction/pathology/physiopathology/*therapy ; Myocardium/cytology/pathology ; Myocytes, Cardiac/*cytology/physiology ; Phenotype ; Regenerative Medicine/methods ; S100 Proteins/genetics/metabolism ; Tail/cytology ; Transcription Factors/genetics/*metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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