Immunocytochemical localization of opsin, visual arrestin, myosin III, and calmodulin in Limulus lateral eye retinular cells and ventral photoreceptors

被引:32
作者
Battelle, BA
Dabdoub, A
Malone, MA
Andrews, AW
Cacciatore, C
Calman, BG
Smith, WC
Payne, R
机构
[1] Univ Florida, Whitney Lab, St Augustine, FL 32080 USA
[2] Univ Florida, Dept Neurosci, St Augustine, FL 32080 USA
[3] Univ Maryland, Dept Biol, College Pk, MD 20742 USA
关键词
phototransduction; rhodopsin; rhabdom; NINAC; unconventional myosins; endocytosis;
D O I
10.1002/cne.1203
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The photoreceptors of the horseshoe crab Limulus polyphemus are classical preparations for studies of the photoresponse and its modulation by circadian clocks. An extensive literature details their physiology and ultrastructure, but relatively little is known about their biochemical organization largely because of a lack of antibodies specific for Limulus photoreceptor proteins. We developed antibodies directed against Limulus opsin, visual arrestin, and myosin III, and we have used them to examine the distributions of these proteins in the Limulus visual system. We also used a commercial antibody to examine the distribution of calmodulin in Limulus photoreceptors. Fixed frozen sections of lateral eye were examined with conventional fluorescence microscopy; ventral photoreceptors were studied with confocal microscopy. Opsin, visual arrestin, myosin III, and calmodulin are all concentrated at the photosensitive rhabdomeral membrane, which is consistent with their participation in the photoresponse. Opsin and visual arrestin, but not myosin III or calmodulin, are also concentrated in extra-rhabdomeral vesicles thought to contain internalized rhabdomeral membrane. In addition, visual arrestin and myosin III were found widely distributed in the cytosol of photoreceptors, suggesting that they have functions in addition to their roles in phototransduction. Our results both clarify and raise new questions about the functions of opsin, visual arrestin, myosin III, and calmodulin in photoreceptors and set the stage for future studies of the impact of light and clock signals on the structure and function of photoreceptors. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:211 / 225
页数:15
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