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大鼠生精小管发育过程中支持细胞特异性分泌蛋白的时间性出现和周期性行为。

Temporal appearance and cyclic behavior of Sertoli cell-specific secretory proteins during the development of the rat seminiferous tubule.

作者信息

Shabanowitz R B, DePhilip R M, Crowell J A, Tres L L, Kierszenbaum A L

出版信息

Biol Reprod. 1986 Oct;35(3):745-60. doi: 10.1095/biolreprod35.3.745.

Abstract

Electrophoretic and morphologic methods have been used to study the time course of [35S] methionine-labeled proteins accumulated in the incubation medium of rat fetal testes and seminiferous cords/tubules during their development. We have found that Sertoli cell-specific secretory proteins S70, S45 and S35 became progressively prominent as premeiotic, meiotic and postmeiotic spermatogenic events were established in the seminiferous tubules. In the sexually mature rat, S70, S45 and S35 were expressed in a spermatogenic stage-dependent manner. While S70, S45 and S35 were present in Stage VII-VIII, S45 and S35 were observed in Stages X and XIV. Neither S70, S45 nor S35 were detected in Stage IV. A relevant group of high molecular weight proteins, previously reported as characteristic products of cultured peritubular cells, accumulated in the incubation medium of seminiferous cords from postnatal Day 0-15 rats. This group of high molecular weight proteins appears when peritubular cells are proliferative and are engaged in the organization of the seminiferous tubular wall. A low molecular weight protein, designated T35, was also detected. T35 was prominent in the medium of incubated fetal testes and seminiferous cords of postnatal rats 0- to 5-days-old and disappeared gradually thereafter. A set of proteins (designated SP1 and SP2) previously ascribed to both cultured Sertoli and peritubular cells, were recognized during the early postnatal stages of seminiferous tubular development. SP1 and SP2 displayed age-dependent fluctuations in their [35S] methionine labeling. The timing of appearance of S70, S45, and S35 indicates both age- and spermatogenic stage-related activity that, in the future, may prove to be functionally significant in the spermatogenic process.

摘要

电泳和形态学方法已被用于研究在大鼠胎儿睾丸和生精索/生精小管发育过程中,[35S]甲硫氨酸标记的蛋白质在孵育培养基中积累的时间进程。我们发现,随着生精小管中减数分裂前、减数分裂和减数分裂后精子发生事件的建立,支持细胞特异性分泌蛋白S70、S45和S35逐渐变得突出。在性成熟大鼠中,S70、S45和S35以精子发生阶段依赖性方式表达。虽然S70、S45和S35存在于VII - VIII期,但在X期和XIV期观察到S45和S35。在IV期未检测到S70、S45和S35。一组先前报道为培养的睾丸周细胞特征性产物的高分子量蛋白质,在出生后0 - 15天大鼠的生精索孵育培养基中积累。当睾丸周细胞增殖并参与生精小管壁的组织时,这组高分子量蛋白质出现。还检测到一种低分子量蛋白质,命名为T35。T35在出生后0至5天大的大鼠胎儿睾丸和生精索的孵育培养基中很突出,此后逐渐消失。一组先前归因于培养的支持细胞和睾丸周细胞的蛋白质(命名为SP1和SP2),在生精小管发育的出生后早期阶段被识别。SP1和SP2在[35S]甲硫氨酸标记中显示出年龄依赖性波动。S70、S45和S35出现的时间表明了与年龄和精子发生阶段相关的活性这两者,在未来,可能在精子发生过程中被证明具有功能意义。

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