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微管正端结合蛋白EB1参与睾丸生精小管中支持细胞的可塑性。

The microtubule plus end-binding protein EB1 is involved in Sertoli cell plasticity in testicular seminiferous tubules.

作者信息

Wang Fubin, Zhang Qiangge, Cao Jingli, Huang Qiongping, Zhu Xueliang

机构信息

Laboratory of Molecular Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.

出版信息

Exp Cell Res. 2008 Jan 1;314(1):213-26. doi: 10.1016/j.yexcr.2007.09.022. Epub 2007 Oct 5.

Abstract

Sertoli cells of testis belong to a unique type of polarized epithelial cells and are essential for spermatogenesis. They form the blood-testis barrier at the base of seminiferous tubule. Their numerous long, microtubule-rich processes extend inward and associate with developing germ cells to sustain germ cell growth and differentiation. How Sertoli cells develop and maintain their elaborate processes has been an intriguing question. Here we showed that, by microinjecting lentiviral preparations into mouse testes of 29 days postpartum, we were able to specifically label individual Sertoli cells with GFP, thus achieving a clear view of their natural configurations together with associated germ cells in situ. Moreover, compared to other microtubule plus end-tracking proteins such as CLIP-170 and p150(Glued), EB1 was highly expressed in Sertoli cells and located along microtubule bundles in Sertoli cell processes. Stable overexpression of a GFP-tagged dominant-negative EB1 mutant disrupted microtubule organizations in cultured Sertoli cells. Furthermore, its overexpression in testis Sertoli cells altered their shapes. Sertoli cells in situ became rod-like, with decreased basal and lateral cell processes. Seminiferous tubule circularity and germ cell number were also reduced. These data indicate a requirement of proper microtubule arrays for Sertoli cell plasticity and function in testis.

摘要

睾丸支持细胞属于一种独特类型的极化上皮细胞,对精子发生至关重要。它们在生精小管基部形成血睾屏障。其众多富含微管的长突起向内延伸,并与发育中的生殖细胞相关联,以维持生殖细胞的生长和分化。支持细胞如何发育并维持其复杂的突起一直是一个引人入胜的问题。在这里我们表明,通过将慢病毒制剂显微注射到产后29天的小鼠睾丸中,我们能够用绿色荧光蛋白(GFP)特异性标记单个支持细胞,从而在原位清晰地观察到它们与相关生殖细胞的自然形态。此外,与其他微管正端追踪蛋白如CLIP-170和p150(Glued)相比,EB1在支持细胞中高度表达,并沿着支持细胞突起中的微管束定位。绿色荧光蛋白标记的显性负性EB1突变体的稳定过表达破坏了培养的支持细胞中的微管组织。此外,其在睾丸支持细胞中的过表达改变了它们的形状。原位支持细胞变成杆状,基底和侧面细胞突起减少。生精小管的圆形度和生殖细胞数量也减少。这些数据表明,睾丸中支持细胞的可塑性和功能需要适当的微管阵列。

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