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光感受器纤毛柄中的肌动蛋白网络在新的外节盘的生成中发挥作用。

The actin network in the ciliary stalk of photoreceptors functions in the generation of new outer segment discs.

作者信息

Hale I L, Fisher S K, Matsumoto B

机构信息

Neuroscience Research Institute, University of California, Santa Barbara 93106, USA.

出版信息

J Comp Neurol. 1996 Dec 2;376(1):128-42. doi: 10.1002/(SICI)1096-9861(19961202)376:1<128::AID-CNE8>3.0.CO;2-5.

Abstract

Cytochalasin D (CD) interferes with the morphogenesis of outer segment disc membrane in photoreceptors. Disruption of either the actin network in the ciliary stalk, where membrane evagination is initiated, or the actin core of the calycal processes, whose position could define the disc perimeter, could be responsible. We have attempted to determine which of these local F-actin populations is involved in membrane morphogenesis and what step in the process is actin-dependent. Biocytin accumulation in nascent discs, detected by fluorescent avidin and laser scanning confocal microscopy (LSCM), provided a means of labeling abnormal discs and a measure of disc membrane addition. F-actin content and distribution were assessed using fluorescent phalloidin and LSCM. First, we examined the effects of a range of CD dosages (0.1, 1.0, or 10.0 microM) on rod photoreceptors in Xenopus laevis eyecup cultures. Ectopic outgrowth of discs, evaluated by LSCM and transmission electron microscopy (TEM), occurred at each concentration. Phalloidin labeling intensified in the ciliary stalk with increasing CD concentration, indicating F-actin aggregation. In contrast, it diminished in the calycal processes, indicating dispersal; TEM showed that calycal process collapse ensued. Disruption was evident at a lower concentration in the ciliary stalk (0.1 microM) than in the calycal processes (1.0 microM). TEM confirmed that the calycal processes remained intact at 0.1 microM. Thus, CD's action on the ciliary stalk network is sufficient to disrupt disc morphogenesis. Second, we examined the effect of CD on temperature-induced acceleration of the rate of disc formation. In the absence of CD, a 10 degrees C temperature shift increased the disc formation rate nearly three-fold. CD (5 microM) caused a 94% inhibition (P < 0.025) of this response; yet, the rate of membrane addition to ectopically growing discs exhibited the expected three-fold increase. Thus, CD's action interferes with the generation of new discs.

摘要

细胞松弛素D(CD)会干扰光感受器中外段盘膜的形态发生。睫状柄中的肌动蛋白网络(膜内陷在此处起始)或萼状突的肌动蛋白核心(其位置可确定盘的周长)受到破坏都可能是原因所在。我们试图确定这些局部F - 肌动蛋白群体中哪一个参与了膜形态发生,以及该过程中的哪一步是肌动蛋白依赖性的。通过荧光抗生物素蛋白和激光扫描共聚焦显微镜(LSCM)检测新生盘中的生物胞素积累,提供了一种标记异常盘的方法以及衡量盘膜添加的指标。使用荧光鬼笔环肽和LSCM评估F - 肌动蛋白的含量和分布。首先,我们研究了一系列CD剂量(0.1、1.0或10.0微摩尔)对非洲爪蟾眼杯培养物中视杆光感受器的影响。通过LSCM和透射电子显微镜(TEM)评估,在每个浓度下都出现了盘的异位生长。随着CD浓度增加,鬼笔环肽标记在睫状柄中增强,表明F - 肌动蛋白聚集。相反,在萼状突中它减少,表明分散;TEM显示随后萼状突塌陷。在睫状柄中较低浓度(0.1微摩尔)时就出现破坏,而在萼状突中则需1.0微摩尔。TEM证实,在0.1微摩尔时萼状突保持完整。因此,CD对睫状柄网络的作用足以破坏盘的形态发生。其次,我们研究了CD对温度诱导的盘形成速率加速的影响。在没有CD的情况下,10℃的温度变化使盘形成速率增加近三倍。CD(5微摩尔)对此反应产生了94%的抑制(P < 0.025);然而,向异位生长的盘中添加膜的速率显示出预期的三倍增加。因此,CD的作用干扰了新盘的产生。

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