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EB1 在雄性大鼠的支持细胞血睾屏障中调节微管和肌动蛋白细胞骨架网络:一项体外研究。

EB1 regulates tubulin and actin cytoskeletal networks at the sertoli cell blood-testis barrier in male rats: an in vitro study.

机构信息

The Mary M. Wohlford Laboratory for Male Contraceptive Research (E.I.T., K.-W.M., C.Y.C.), Center for Biomedical Research, Population Council, New York, New York 10065; and School of Biological Sciences (W.M.L.), University of Hong Kong, Hong Kong, China.

出版信息

Endocrinology. 2015 Feb;156(2):680-93. doi: 10.1210/en.2014-1720. Epub 2014 Dec 2.

Abstract

During spermatogenesis, developing germ cells are transported across the seminiferous epithelium. Studies propose that because microtubules (MTs) serve as the tracks for transporting cell organelles, they may also serve a similar function in the transport of developing germ cells. Polarized MTs may provide the tracks along which polarized actin microfilaments, which act as vehicles to transport cargo, such as preleptotene spermatocytes through the blood-testis barrier (BTB) and spermatids across the epithelium. Yet the molecular mechanism(s) underlying these events remain unknown. Using an established in vitro Sertoli cell system to study BTB function, we demonstrated herein that a MT regulatory protein end-binding protein 1 (EB1) regulates the MT- and also the actin-based cytoskeleton of the Sertoli cell BTB in the rat. EB1 serves as a coordinator between the two cytoskeletons by regulating MT polymerization and actin filament bundling to modulate germ cell transport at the Sertoli cell BTB. A knockdown of EB1 by RNA interference was found to perturb the tight junction (TJ)-permeability barrier, as evidenced by mislocalization of junctional proteins critical for barrier function to facilitate spermatocyte transport, which was likely achieved by two coordinated events. First, EB1 knockdown resulted in changes in MT polymerization, thereby perturbing MT organization in Sertoli cells in which polarized MT no longer stretched properly across the cell cytosol to serve as the tracks. Second, EB1 knockdown perturbed actin organization via its effects on the branched actin polymerization-inducing protein called Arp3 (actin-related protein 3), perturbing microfilament bundling capability based on a biochemical assay, thereby causing microfilament truncation and misorganization, disrupting the function of the vehicle. This reduced actin microfilament bundling capability thus perturbed TJ-protein distribution and localization at the BTB, destabilizing the TJ barrier, leading to its remodeling to facilitate spermatocyte transport. In summary, EB1 provides a functional link between tubulin- and actin-based cytoskeletons to confer spermatocyte transport at the BTB.

摘要

在精子发生过程中,发育中的生殖细胞被运输穿过生精上皮。研究表明,由于微管(MTs)作为细胞器运输的轨道,它们在发育中的生殖细胞运输中也可能发挥类似的作用。极化的 MT 可能提供轨道,沿着该轨道极化的肌动蛋白微丝作为运输货物的载体,例如预减数分裂精母细胞穿过血睾屏障(BTB)和精子穿过上皮细胞。然而,这些事件背后的分子机制尚不清楚。我们使用已建立的体外支持细胞系统来研究 BTB 功能,在此证明微管调节蛋白末端结合蛋白 1(EB1)调节大鼠支持细胞 BTB 的 MT 和肌动蛋白细胞骨架。EB1 通过调节 MT 聚合和肌动蛋白丝束集来协调两个细胞骨架,从而调节生殖细胞在支持细胞 BTB 的运输,这可能通过两个协调的事件来实现。首先,EB1 的 RNA 干扰敲低导致紧密连接(TJ)-通透性屏障的破坏,这表现在对屏障功能至关重要的连接蛋白的定位错误,以促进精母细胞的运输,这可能是通过两个协调的事件实现的。首先,EB1 敲低导致 MT 聚合的变化,从而扰乱了极化 MT 不再正确地延伸穿过细胞胞质溶胶作为轨道的支持细胞中的 MT 组织。其次,EB1 敲低通过其对称为 Arp3(肌动蛋白相关蛋白 3)的分支肌动蛋白聚合诱导蛋白的影响扰乱了肌动蛋白组织,通过生化测定扰乱了微丝束集能力,从而导致微丝截断和组织紊乱,破坏了载体的功能。这种减少的肌动蛋白微丝束集能力因此扰乱了 TJ 蛋白在 BTB 的分布和定位,破坏了 TJ 屏障的稳定性,导致其重塑以促进精母细胞的运输。总之,EB1 为微管和肌动蛋白细胞骨架之间提供了一个功能联系,以赋予 BTB 处的精母细胞运输。

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