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视网膜脱离对培养的青蛙视网膜中视杆细胞盘膜组装的影响。

Effects of retinal detachment on rod disc membrane assembly in cultured frog retinas.

作者信息

Hale I L, Fisher S K, Matsumoto B

机构信息

Department of Biological Sciences, University of California, Santa Barbara 93106.

出版信息

Invest Ophthalmol Vis Sci. 1991 Oct;32(11):2873-81.

PMID:1833357
Abstract

The authors compared rod outer segment (ROS) disc membrane assembly rates in detached and attached frog retinas to determine if there was a rapid impairment of membrane assembly in response to retinal detachment. Membrane assembly was quantified in vitro by incubating retinas in medium containing Lucifer yellow, which is entrapped by nascent discs. Video microscopy was used to detect incorporation of the dye. During the first 10 hr after separation of the retina from the retinal pigment epithelium (RPE), ROS-disc membrane assembly in isolated Xenopus laevis neural retinas continued at a near normal rate, 0.81 microns/10 hr, a 13% reduction (P less than .01), compared with the 0.93 microns/10 hr observed in attached control retinas. The morphology of the OS appeared normal in most rod photoreceptors by transmission electron microscopy, although vesiculation of the most basal OS membranes was seen in a small population (25%) of rods. Approximately 90% of rod photoreceptors continued to assemble OS membranes for more than 10 hr after detachment, but by the end of 2 days, only 55% were still making new discs. The percentage of rods with normal basal OS membranes also decreased (to approximately 50%). Therefore, only 25% were assembling morphologically normal discs 2 days after detachment. In attached control regions, rod photoreceptors showed a comparatively minor response to culture conditions; assembly of morphologically normal discs continued for 2 days in about 85% and ceased in only 10%. These results indicate that the effects on disc membrane assembly of disrupting photoreceptor-RPE interaction in vitro initially are slight but become progressively severe with time.

摘要

作者比较了分离和附着状态下青蛙视网膜中视杆细胞外段(ROS)盘膜组装速率,以确定视网膜脱离后膜组装是否会迅速受损。通过将视网膜置于含有荧光素黄的培养基中孵育来体外定量膜组装,荧光素黄会被新生的盘所捕获。使用视频显微镜检测染料的掺入情况。在视网膜与视网膜色素上皮(RPE)分离后的最初10小时内,分离的非洲爪蟾神经视网膜中的ROS盘膜组装以接近正常的速率持续进行,为0.81微米/10小时,与附着的对照视网膜中观察到的0.93微米/10小时相比,降低了13%(P小于0.01)。透射电子显微镜观察显示,大多数视杆光感受器的视杆细胞外段(OS)形态正常,尽管在一小部分(25%)视杆细胞中可见最基部的OS膜出现囊泡化。大约90%的视杆光感受器在脱离后继续组装OS膜超过10小时,但到2天结束时,只有55%仍在形成新的盘。具有正常基部OS膜的视杆细胞百分比也下降(至约50%)。因此,脱离2天后只有25%的视杆细胞在组装形态正常的盘。在附着的对照区域,视杆光感受器对培养条件的反应相对较小;形态正常的盘的组装在约85%的细胞中持续2天,仅10%的细胞停止组装。这些结果表明,体外破坏光感受器与RPE的相互作用对盘膜组装的影响最初较小,但随着时间的推移会逐渐变得严重。

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