GC1 deletion prevents light-dependent arrestin translocation in mouse cone photoreceptor cells.

Invest Ophthalmol Vis Sci

Department of Neuroscience, McKnight Brain Institute and College of Medicine, University of Florida, Gainesville, Florida 32610-0255, USA.

Published: January 2005

Purpose: Light-driven translocation of phototransduction regulatory proteins between the inner and outer segments of photoreceptor cells plays a role in the adaptation of these cells to light. The purpose of this study was to examine the effects of the absence of guanylate cyclase 1 (GC1) on light-driven protein translocation in rod and cone cells. Both cell types express GC1, but differ in sensitivity, saturation, and response times to light.

Methods: Immunohistochemical techniques employing antibodies specific for cone and rod transducin alpha (Talpha) subunits and arrestins were used to examine light-driven translocation of these proteins in the retinas of wild-type and GC1 knockout (KO) mice.

Results: Translocation of cone arrestin from cone outer segments to the inner cell regions was disrupted in the absence of GC1, whereas translocation of arrestin and Talpha in rods was not affected. Cone Talpha did not translocate in wild-type and GC1 KO mice, but differed in its subcellular distribution in GC1 KO retina, remaining in the cone outer segment in light and in dark.

Conclusions: These results suggest that multiple, independent pathways regulate the translocation of phototransduction proteins and that GC1, and presumably cGMP, are of key importance in signaling the translocation of cone arrestin.

Download full-text PDF

Source
http://dx.doi.org/10.1167/iovs.04-0691DOI Listing

Publication Analysis

Top Keywords

gc1
8
translocation
8
cone
8
photoreceptor cells
8
light-driven translocation
8
translocation phototransduction
8
outer segments
8
wild-type gc1
8
translocation cone
8
cone arrestin
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!