Publikationsdatum:
2005-10-08
Beschreibung:
To investigate the role of astrocytes in regulating synaptic transmission, we generated inducible transgenic mice that express a dominant-negative SNARE domain selectively in astrocytes to block the release of transmitters from these glial cells. By releasing adenosine triphosphate, which accumulates as adenosine, astrocytes tonically suppressed synaptic transmission, thereby enhancing the dynamic range for long-term potentiation and mediated activity-dependent, heterosynaptic depression. These results indicate that astrocytes are intricately linked in the regulation of synaptic strength and plasticity and provide a pathway for synaptic cross-talk.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pascual, Olivier -- Casper, Kristen B -- Kubera, Cathryn -- Zhang, Jing -- Revilla-Sanchez, Raquel -- Sul, Jai-Yoon -- Takano, Hajime -- Moss, Stephen J -- McCarthy, Ken -- Haydon, Philip G -- New York, N.Y. -- Science. 2005 Oct 7;310(5745):113-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neuroscience, Conte Center for Integration at the Tripartite Synapse, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16210541" target="_blank"〉PubMed〈/a〉
Schlagwort(e):
Adenosine/*metabolism
;
Adenosine A1 Receptor Antagonists
;
Adenosine Triphosphatases/antagonists & inhibitors
;
Adenosine Triphosphate/analogs & derivatives/metabolism/pharmacology
;
Animals
;
Astrocytes/drug effects/*physiology
;
Cells, Cultured
;
Excitatory Postsynaptic Potentials
;
Hippocampus/drug effects/physiology
;
In Vitro Techniques
;
Long-Term Potentiation/drug effects
;
Mice
;
Mice, Transgenic
;
Neuronal Plasticity/drug effects
;
Purinergic P1 Receptor Antagonists
;
Purinergic P2 Receptor Antagonists
;
Receptor, Adenosine A1/metabolism
;
Receptors, N-Methyl-D-Aspartate/antagonists & inhibitors/metabolism
;
Receptors, Purinergic P1/metabolism
;
Receptors, Purinergic P2/metabolism
;
Synapses/*physiology
;
*Synaptic Transmission/drug effects
;
Xanthines/pharmacology
Print ISSN:
0036-8075
Digitale ISSN:
1095-9203
Thema:
Biologie
,
Chemie und Pharmazie
,
Informatik
,
Medizin
,
Allgemeine Naturwissenschaft
,
Physik
Permalink
