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视杆光感受器远端末梢的细胞骨架特化结构。

Cytoskeletal specializations at the rod photoreceptor distal tip.

作者信息

Roof D, Adamian M, Jacobs D, Hayes A

机构信息

Berman-Gund Laboratory for the Study of Retinal Degenerations, Harvard Medical School, Boston, Massachusetts.

出版信息

J Comp Neurol. 1991 Mar 8;305(2):289-303. doi: 10.1002/cne.903050210.

DOI:10.1002/cne.903050210
PMID:1902849
Abstract

We have examined microtubules and microtubule-like elements within the toad rod photoreceptor outer segment in order to define regional specializations of the photoreceptor cytoskeleton. "Ciliary" microtubules were localized within the rod outer segment (ROS) by using thin section electron microscopy, immunofluorescence, and rapid-freeze deep-etch microscopy. All three methods showed that ciliary microtubules stop short of the extreme ROS distal tip, although abundant microtubule-like structures distinct from the ciliary microtubules were found within the distal 10-15 microns of the ROS tip. These heretofore undescribed "distal ROS tubules" are clustered at the clefts or incisures of the disk membrane stack and resemble microtubules in overall size and shape, although they are not closely related antigenically to tubulin. The distal ROS tubules are more abundant in green rods than red rods and vary in number during the daily light/dark cycle. Quantitation of these tubules at two time points during the light/dark cycle suggests that there are three- to fourfold more tubules in the ROS tip one hour after light onset than one hour before light onset. Retinas prevented from normal disk membrane shedding by separation of the retina from the adjacent pigment epithelium, failed to develop increased numbers of tubules after light onset. This suggests that the newly described distal ROS tubules may modulate or be modulated by light-induced interactions between the photoreceptors and pigment epithelium, such as those that occur during the disk shedding phase of membrane turnover.

摘要

为了明确光感受器细胞骨架的区域特化,我们研究了蟾蜍视杆光感受器外段内的微管和类微管成分。通过超薄切片电子显微镜、免疫荧光和快速冷冻深度蚀刻显微镜技术,“纤毛”微管定位在了视杆外段(ROS)内。所有这三种方法都表明,纤毛微管在ROS的最远端末梢之前就终止了,尽管在ROS末梢的远端10 - 15微米范围内发现了大量与纤毛微管不同的类微管结构。这些此前未被描述的“远端ROS微管”聚集在盘膜堆叠的裂缝或切迹处,在总体大小和形状上类似于微管,尽管它们在抗原性上与微管蛋白没有密切关系。远端ROS微管在绿色视杆中比红色视杆中更丰富,并且在日常的光/暗周期中数量会发生变化。在光/暗周期的两个时间点对这些微管进行定量分析表明,光照开始后一小时,ROS末梢中的微管数量比光照开始前一小时多三到四倍。通过将视网膜与相邻色素上皮分离而阻止正常盘膜脱落的视网膜,在光照开始后未能产生更多数量的微管。这表明新描述的远端ROS微管可能会调节或被光感受器与色素上皮之间的光诱导相互作用所调节,比如在膜更新的盘膜脱落阶段发生的那些相互作用。

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J Comp Neurol. 1991 Mar 8;305(2):289-303. doi: 10.1002/cne.903050210.
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