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发动蛋白1和发动蛋白2在球管复合体形成及精子细胞释放中的作用

Implication of amphiphysin 1 and dynamin 2 in tubulobulbar complex formation and spermatid release.

作者信息

Kusumi Norihiro, Watanabe Masami, Yamada Hiroshi, Li Shun-Ai, Kashiwakura Yuji, Matsukawa Takashi, Nagai Atsushi, Nasu Yasutomo, Kumon Hiromi, Takei Kohji

机构信息

Department of Urology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.

出版信息

Cell Struct Funct. 2007;32(2):101-13. doi: 10.1247/csf.07024. Epub 2007 Aug 31.

Abstract

Tubulobulbar complexes (TBCs) are composed of several tubular invaginations formed at the plasma membrane of testicular Sertoli cells. TBCs are transiently formed at the contact region with spermatids at spermatogenic stage VII in rat and mouse, and such TBC formation is prerequisite for spermatid release. Since the characteristic structure of TBCs suggests that the molecules implicated in endocytosis could be involved in TBC formation, we here investigated the localization and physiological roles of endocytic proteins, amphiphysin 1 and dynamin 2, at TBCs. We demonstrated by immunofluorescence that the endocytic proteins were concentrated at TBCs, where they colocalized with cytoskeletal proteins, such as actin and vinculin. Immunoelectron microscopy disclosed that both amphiphysin 1 and dynamin 2 were localized on TBC membrane. Next, we histologically examined the testis from amphiphysin 1 deficient {Amph(-/-)} mice. Morphometric analysis revealed that the number of TBCs was significantly reduced in Amph(-/-). The ratio of stage VIII seminiferous tubules was increased, and the ratio of stage IX was conversely decreased in Amph(-/-). Moreover, unreleased spermatids in stage VIII seminiferous tubules were increased in Amph(-/-), indicating that spermatid release and the following transition from stage VIII to IX was prolonged in Amph(-/-) mice. These results suggest that amphiphysin 1 and dynamin 2 are involved in TBC formation and spermatid release at Sertoli cells.

摘要

管球复合体(TBCs)由睾丸支持细胞质膜上形成的几个管状内陷组成。在大鼠和小鼠的生精阶段VII,TBCs在与精子细胞的接触区域短暂形成,而这种TBC的形成是精子细胞释放的先决条件。由于TBCs的特征结构表明参与内吞作用的分子可能与TBC的形成有关,我们在此研究了内吞蛋白发动蛋白1和发动蛋白2在TBCs处的定位和生理作用。我们通过免疫荧光证明,内吞蛋白集中在TBCs处,在那里它们与细胞骨架蛋白如肌动蛋白和纽蛋白共定位。免疫电子显微镜显示,发动蛋白1和发动蛋白2都定位于TBC膜上。接下来,我们对发动蛋白1缺陷型(Amph(-/-))小鼠的睾丸进行了组织学检查。形态计量分析显示,Amph(-/-)小鼠中TBCs的数量显著减少。在Amph(-/-)小鼠中,VIII期生精小管的比例增加,而IX期的比例则相反降低。此外,在Amph(-/-)小鼠的VIII期生精小管中未释放的精子细胞增加,这表明在Amph(-/-)小鼠中精子细胞的释放以及随后从VIII期到IX期的转变延长。这些结果表明,发动蛋白1和发动蛋白2参与支持细胞中TBC的形成和精子细胞的释放。

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