支持细胞的旁分泌作用。

Medical biology Pub Date : 1986-01-01
J M Saez, E Tabone, M H Perrard-Sapori, M A Rivarola
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引用次数: 0

摘要

来自几个实验方法的数据强烈表明,支持细胞对睾丸的两个主要功能,雄激素分泌和精子发生施加旁分泌控制。通过将支持细胞与其他睾丸细胞共培养,获得了支持细胞这一作用的进一步证据。猪或大鼠支持细胞与猪间质细胞共培养可增加hCG受体数量,并增加间质细胞的类固醇生成活性。FSH预处理进一步提高了这两个参数的值。这些生化变化与间质细胞的超微结构变化有关。支持细胞对间质细胞的影响取决于两种细胞的比例和培养细胞的基质。此外,间质细胞产生FSH受体数量的增加,并通过支持细胞产生FSH刺激纤溶酶原激活剂。将大鼠或猪支持细胞与大鼠生殖细胞共培养,可诱导生殖细胞RNA和DNA生物合成活性的提高。大多数刺激作用似乎是由支持细胞分泌的扩散因子介导的,但当生殖细胞与其他细胞接触时,可以观察到刺激作用的充分表达。在这个共培养系统中,含有成熟精子细胞的部分大鼠生殖细胞抑制了大鼠支持细胞RNA和DNA的合成,但对猪支持细胞没有影响。相反,一小部分富含精原细胞和preleptotene精母细胞的大鼠生殖细胞可以刺激大鼠支持细胞DNA合成,但对猪支持细胞没有影响。这些结果清楚地表明,支持细胞对间质和非种特异性生殖细胞的刺激作用主要是由扩散因子介导的,其分泌受卵泡刺激素调节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Paracrine role of Sertoli cells.

Data from several experimental approaches strongly suggest that Sertoli cells exert a paracrine control of the two main testicular functions, androgen secretion and spermatogenesis. Further evidence supporting this role of Sertoli cells was obtained by coculture of Sertoli cells with other testicular cells. Coculture of pig or rat Sertoli cells with pig Leydig cells produces an increase in the hCG receptor number and an increase in the steroidogenic activity of Leydig cells. Pretreatment with FSH further increases the values of these two parameters. These biochemical changes were associated with ultrastructural changes in Leydig cells. The effects of Sertoli cells on Leydig cells depend upon the ratio of the two cells and on the substrate in which the cells are cultured. Moreover, Leydig cells produce an increase in the FSH receptor number and in the FSH stimulation of plasminogen activator production by Sertoli cells. Coculture of rat or pig Sertoli cells with rat germ cells, induces an increase in the RNA and DNA biosynthetic activities of germ cells. Most of the stimulatory effects seemed to be mediated by diffusible factors, secreted by Sertoli cells, but full expression of the stimulatory action was observed when germ cells were in contact with other cells. In this coculture system, a fraction of rat germ cells containing mainly mature forms of spermatocytes inhibited rat Sertoli cell RNA and DNA synthesis, but had no effect on pig Sertoli cells. On the contrary, a fraction of rat germ cells richer in spermatogonias and preleptotene spermatocytes, stimulated rat Sertoli cell DNA synthesis but was without effect on pig Sertoli cells. These results clearly show that the stimulatory effects of Sertoli cells on Leydig and on germ cells which are not species specific are mediated mainly by diffusible factors, the secretion of which is regulates by FSH.

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