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17β-雌二醇处理后大鼠生精上皮细胞中间丝蛋白 vimentin 的磷酸化和分布状态的改变。

Altered phosphorylation and distribution status of vimentin in rat seminiferous epithelium following 17β-estradiol treatment.

机构信息

Neuroendocrinology Division, National Institute for Research in Reproductive Health, Parel, Mumbai, India.

出版信息

Histochem Cell Biol. 2011 Nov;136(5):543-55. doi: 10.1007/s00418-011-0856-5. Epub 2011 Sep 14.

Abstract

Vimentin, type III intermediate filament, has stage-specific localization in the Sertoli cell. In the rat, during stages I-V and XI-XIV of the seminiferous epithelium, vimentin is localized in the perinuclear area with filaments projecting into the apical region toward the developing germ cells. These filaments decrease in length at stages VI-VII with perinuclear staining in stages VIII-IX, when spermiation occurs. Our earlier studies following 17β-estradiol treatment to adult male rats demonstrated an increase in germ cell apoptosis, spermiation failure and disruption of Sertoli cell microfilaments and microtubules. The present study was undertaken to determine the stage-specific distribution of vimentin and its involvement in spermiation failure and germ cell apoptosis. Immunofluorescence studies revealed that in contrast to the perinuclear localization with small extensions in control stages VII-IX, long extensions radiating apically to the spermatids in deep recess were observed in the treated group. Immunoprecipitation studies showed marked absence of phosphorylated vimentin in stages VII-VIII in the treated group. Further, localization of plectin, cytoskeletal linker protein, showed decrease in all the stages of spermatogenesis following estradiol treatment. Interestingly, for the first time the localization of plectin in the tubulobulbar complex was observed. In conclusion, the study suggests that estradiol treatment leads to an effect on vimentin phosphorylation, which could have inhibited the disassembly of vimentin leading to retention of apical projection in stages VII-VIII. These effects could be presumably due to a decrease in plectin, affecting the reorganization of vimentin and therefore the apical movement of spermatids, leading to spermiation failure.

摘要

波形蛋白是 III 型中间丝,在支持细胞中有阶段特异性定位。在大鼠中,在生精上皮的 I-V 期和 XI-XIV 期,波形蛋白定位于核周区,其丝突伸向朝向发育中的精母细胞的顶端区。这些丝突在 VI-VII 期变短,在 VIII-IX 期出现核周染色,此时发生精子发生。我们之前的研究表明,在成年雄性大鼠中用 17β-雌二醇处理后,精母细胞凋亡增加,精子发生失败,支持细胞微丝和微管破坏。本研究旨在确定波形蛋白的阶段特异性分布及其在精子发生失败和精母细胞凋亡中的作用。免疫荧光研究显示,与对照组 VII-IX 期的核周定位和小突起不同,处理组观察到向精子深处放射状的长突起。免疫沉淀研究表明,处理组在 VII-VIII 期磷酸化波形蛋白明显缺失。此外,在雌激素处理后,所有生精阶段的连接蛋白(细胞骨架连接蛋白)定位均减少。有趣的是,首次观察到连接蛋白在小管泡复合体中的定位。总之,该研究表明,雌二醇处理导致波形蛋白磷酸化的影响,这可能抑制了波形蛋白的解体,导致 VII-VIII 期顶端突起的保留。这些影响可能归因于连接蛋白的减少,影响了波形蛋白的重排,因此精子顶端运动,导致精子发生失败。

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