Document Detail


Composition of the GABA(A) receptors of retinal dopaminergic neurons.
MedLine Citation:
PMID:  10479684     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Transgenic technology, single-cell RT-PCR, and immunocytochemistry were combined to investigate the composition of the GABA(A) receptors of dopaminergic (interplexiform) amacrine (DA) cells. A mouse line was used in which these neurons were labeled with human placental alkaline phosphatase and could therefore be identified in vitro after dissociation of the retina. We performed single-cell RT-PCR on the isolated cells and showed that (1) DA cells contained the messages for alpha1, alpha3, alpha4, beta1, beta3, gamma1, gamma2(S), and gamma2(L) subunits; (2) this transcript repertory did not change on dissociation of the retina and throughout the time required for cell harvesting; and (3) all DA cells contained the entire transcript repertory. Immunocytochemistry with subunit-specific antibodies showed that all subunits were expressed and appeared homogeneously distributed throughout the cell membrane at a low concentration. In addition, with the exception of alpha4, the subunits formed clusters at the surface of the dendrites and on the inner pole of the cell body. Because of their size, shape, and topographic coincidence with GABAergic endings, the clusters were interpreted as postsynaptic active zones containing GABA(A) receptors. The composition of the synaptic receptors was not uniform: clusters distributed throughout the dendritic tree contained alpha3, beta3, and, less frequently, beta1 subunits, whereas clusters containing the alpha1 subunit were confined to large dendrites. Therefore, DA cells possess at least two types of GABA(A) receptors localized in different synapses. Furthermore, they exhibit multiple extrasynaptic GABA(A) receptors.
Authors:
S Gustincich; A Feigenspan; W Sieghart; E Raviola
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Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  The Journal of neuroscience : the official journal of the Society for Neuroscience     Volume:  19     ISSN:  1529-2401     ISO Abbreviation:  J. Neurosci.     Publication Date:  1999 Sep 
Date Detail:
Created Date:  1999-10-04     Completed Date:  1999-10-04     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  8102140     Medline TA:  J Neurosci     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  7812-22     Citation Subset:  IM    
Affiliation:
Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, USA.
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MeSH Terms
Descriptor/Qualifier:
Alkaline Phosphatase / analysis,  genetics
Animals
Dopamine / analysis
Humans
Immunohistochemistry
Macromolecular Substances
Mice
Mice, Transgenic
Neurons / cytology,  physiology*
Receptors, GABA-A / analysis*,  chemistry,  genetics*
Restriction Mapping
Retina / cytology,  physiology*
Reverse Transcriptase Polymerase Chain Reaction
Synapses / physiology,  ultrastructure
Transcription, Genetic*
Tyrosine 3-Monooxygenase / analysis,  genetics
Grant Support
ID/Acronym/Agency:
EY-01344/EY/NEI NIH HHS
Chemical
Reg. No./Substance:
0/Macromolecular Substances; 0/Receptors, GABA-A; EC 1.14.16.2/Tyrosine 3-Monooxygenase; EC 3.1.3.1/Alkaline Phosphatase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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