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Stage-Specific Changes in GDNF Expression by Rat Sertoli Cells: A Possible Regulator of the Replication and Differentiation of Stem Spermatogonia

机译:大鼠睾丸支持细胞中GDNF表达的阶段特定变化:干精原细胞复制和分化的可能调节剂。

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摘要

>In the adult testis, the precise control of the self-renewing replication and differentiation of stem spermatogonia is fundamental to male fertility. Previous studies have shown that the replication of A single (As) spermatogonia, a population that includes the stem cells, is maximal at stage I of the cycle of the rat seminiferous epithelium and minimal at stage VII, while the ratio of A-paired spermatogonia to As spermatogonia increases from stages I to VII. It has been hypothesized that these changes in As spermatogonia replication and differentiation result from changes in the expression of glial cell-line derived neurotrophic factor (GDNF) by Sertoli cells. To directly test this hypothesis, we used immunocytochemistry and confocal microscopy to demonstrate that within intact seminiferous tubules, GDNF is detectable only in Sertoli cells and that its amount and its location within these cells changes with progression of the stages of the cycle. The identification of Sertoli cells as the primary source of GDNF was confirmed by RT-PCR analysis of RNA isolated from purified populations of Sertoli cells, pachytene spermatocytes, and round spermatids. Stage-specific changes in GDNF expression were confirmed by quantifying GDNF mRNA in seminiferous tubules at defined stages of the cycle. Expression of this transcript was maximal at stage I, fell 14-fold by stage VIIc,d, and then increased 12-fold by stages XIII–XIV. This pattern of expression was the opposite of the control, cathepsin L mRNA. Taken together, these data support the hypothesis that cyclical changes in GDNF expression by Sertoli cells are responsible for the stage-specific replication and differentiation of stem spermatogonia, the foundational cells of spermatogenesis.
机译:>在成年睾丸中,对精子自我更新复制和分化的精确控制是男性生育的基础。先前的研究表明,包括大鼠干细胞在内的单个单精原细胞的复制在大鼠生精上皮周期的第一阶段最大,而在第七阶段则最小,而A配对的精原细胞的比例则最小。当精原细胞从第一阶段增加到第七阶段时。已经假设As精原细胞复制和分化的这些变化是由Sertoli细胞的神经胶质细胞系衍生的神经营养因子(GDNF)的表达变化引起的。为了直接检验该假设,我们使用了免疫细胞化学和共聚焦显微镜来证明在完整的生精小管中,GDNF仅在Sertoli细胞中可检测到,并且其数量和在这些细胞中的位置随周期阶段的进展而变化。通过从纯化的Sertoli细胞,粗线精原细胞和圆形精子细胞群体中分离的RNA的RT-PCR分析,证实了Sertoli细胞是GDNF的主要来源。 GDNF表达的阶段特异性变化可以通过在周期的定义阶段定量生精小管中的GDNF mRNA来确认。该转录物的表达在I期达到最大,到VIIc,d期下降14倍,然后到XIII–XIV期上升12倍。这种表达方式与对照组织蛋白酶L mRNA相反。综上所述,这些数据支持以下假设:Sertoli细胞在GDNF表达中的周期性变化与精子发生的基础细胞干精原细胞的阶段特异性复制和分化有关。

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