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Distribution of protein kinase C isoforms in the cat retina

Published online by Cambridge University Press:  12 November 2002

BOZENA FYK-KOLODZIEJ
Affiliation:
Department of Anatomy and Cell Biology, Wayne State University, Detroit
WENHUI CAI
Affiliation:
Department of Psychiatry, University of Texas Southwestern Medical Center at Dallas and Dallas VAMC, Dallas
ROBERTA G. POURCHO
Affiliation:
Department of Anatomy and Cell Biology, Wayne State University, Detroit

Abstract

Immunocytochemical localization was carried out for five isoforms of protein kinase C (PKC) in the cat retina. In common with other mammalian species, PKCα was found in rod bipolar cells. Staining was also seen in a small population of cone bipolar cells with axon terminals ramifying near the middle of the inner plexiform layer (IPL). PKCβI was localized to rod bipolar cells, one class of cone bipolar cell, and numerous amacrine and displaced amacrine cells. Staining for PKCβII was seen in three types of cone bipolar cells as well as in amacrine and ganglion cells. Immunoreactivity for both PKCε and PKCζ was found in rod bipolar cells; PKCε was also seen in a population of cone bipolar cells and a few amacrine and ganglion cells whereas PKCζ was found in all ganglion cells. Double-label immunofluorescence studies showed that dendrites of the two PKCβII-positive OFF-cone bipolar cells exhibit immmunoreactivity for the kainate-selective glutamate receptor GluR5. The third PKCβII cone bipolar is an ON-type cell and did not stain for GluR5. The retinal distribution of these isoforms of PKC is consistent with a role in modulation of various aspects of neurotransmission including synaptic vesicle release and regulation of receptor molecules.

Type
Research Article
Copyright
2002 Cambridge University Press

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