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PMID: 1849721 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Localization of the inositol 1,4,5-trisphosphate receptor in synaptic terminals in the vertebrate retina.

Neuron ·Vol. 6 ·No. 4 ·1991-04-00 ·Pages 525-31

Peng YW, Sharp AH, Snyder SH, Yau KW

Abstract

Inositol 1,4,5-trisphosphate (InsP3) mobilizes internal Ca2+ in cells by binding to a receptor protein, which has recently been purified and molecularly cloned. To clarify those neuronal functions that are regulated by InsP3, we have localized this InsP3 receptor protein immunocytochemically in the retina, a neural tissue of well-defined structure and function. Positive staining in neurons is confined almost exclusively to the synaptic layers. Using dissociated retinal neurons, we have further localized the receptor to presynaptic terminals of photoreceptors and bipolar cells, as well as the synaptic processes of amacrine cells. The specific association of InsP3 receptors with synaptic terminals suggests a role for InsP3 in synaptic modulation, especially with respect to transmitter release.

MeSH Terms
Ambystoma Animals Calcium Channels Inositol 1,4,5-Trisphosphate Receptors Nerve Endings/metabolism Neurons/metabolism Rabbits Rats Rats, Inbred Strains Receptors, Cell Surface/metabolism Receptors, Cytoplasmic and Nuclear Retina/cytology,metabolism Synapses/metabolism Tissue Distribution
Chemicals
Calcium Channels Inositol 1,4,5-Trisphosphate Receptors Receptors, Cell Surface Receptors, Cytoplasmic and Nuclear
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Peng Y W
Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Sharp A H
Snyder S H
Yau K W
Article Info
Journal
Neuron
Abbr.
Neuron
ISSN
0896-6273
Published
1991-04-00
Pages
525-31
Language
English
Region
United States
NLM ID
8809320
Subset
IM
Grants
NIDA NIH HHS · DA00074 · United States
NEI NIH HHS · EY06837 · United States
NIMH NIH HHS · MH18531 · United States
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