Gray Shaunté M, Kelly Shannon, Robles Laura J
Department of Biology, California State University, Dominguez Hills, 1000 East Victoria Street, Carson, California 90747, U.S.A.,
Am Malacol Bull. 2008 Dec 1;26(1-2):19-26. doi: 10.4003/006.026.0203.
Light sensitive rhabdoms in the octopus retina increase in cross-sectional area in the dark and shrink in the light. Growth in the dark is due to the formation of microvilli in an avillar region of the photoreceptor cell membrane and lengthening of rhabdomere microvilli already present. Diminution in the light is the result of the disassembly and shortening of the same microvilli. Each microvillus contains an actin filament core that must be assembled or disassembled in the dark or light, respectively. To understand the regulation of the construction and breakdown of rhabdomere microvilli in the light and dark, we used centrifugation to separate the rhabdom membranes followed by Western blotting and Rho pull-down assays to investigate the role of Rho GTPases in this process. Western blotting showed a difference in the distribution of Rho in rhabdom membrane and supernatant fractions. In the light, Rho was mostly present in the supernatant but in the dark it was found in the fraction enriched with rhabdom membranes. Complementing these results, pull-down assays showed that Rho is activated in the dark but in the light, Rho is mostly inactive. We believe that in the dark, activated Rho binds to the rhabdom membrane and initiates signaling pathways, leading to growth of rhabdomere microvilli. In the light, Rho is present in the soluble fraction, is inactivated, and is likely bound to a Rho GDI. Receptors involved in the activation of Rho in the dark are undetermined and may involve rhodopsin or another membrane protein.
章鱼视网膜中的光敏视杆在黑暗中横截面积增大,在光照下缩小。黑暗中的生长是由于光感受器细胞膜无纤毛区域形成微绒毛以及已存在的视杆微绒毛延长。光照下的缩小是相同微绒毛解聚和缩短的结果。每个微绒毛都含有一个肌动蛋白丝核心,该核心必须分别在黑暗或光照下组装或拆卸。为了了解视杆微绒毛在明暗条件下构建和分解的调节机制,我们通过离心分离视杆膜,然后进行蛋白质免疫印迹和Rho下拉分析,以研究Rho GTP酶在这一过程中的作用。蛋白质免疫印迹显示Rho在视杆膜和上清液组分中的分布存在差异。在光照下,Rho主要存在于上清液中,但在黑暗中,它存在于富含视杆膜的组分中。作为这些结果的补充,下拉分析表明Rho在黑暗中被激活,但在光照下,Rho大多处于无活性状态。我们认为,在黑暗中,激活的Rho与视杆膜结合并启动信号通路,导致视杆微绒毛生长。在光照下,Rho存在于可溶性组分中,处于无活性状态,并且可能与一种Rho鸟苷酸解离抑制蛋白结合。在黑暗中参与激活Rho的受体尚未确定,可能涉及视紫红质或另一种膜蛋白。