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Presence of Metastasis-associated Protein 1 in Sertoli Cells is Required for Proper Contact Between Sertoli Cells and Adjacent Germ Cells

机译:Sertoli细胞和相邻的生殖细胞之间的正确接触需要在Sertoli细胞中存在与转移相关的蛋白1。

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To investigate whether the normal expression of metastasis-associated protein 1 (MTA1) in Sertoli cells (SCs) is associated with adjacent germ cells (OCs) and to provide the functional relevance of MTA1 in this somatic cell.The expression pattern of MTA1 in the SCs of impaired human spermatogenesis was determined using immunohistochemistry. The effect of the depletion of GCs on the expression of MTA1 in isolated SCs was evaluated using reverse transcriptase polymerase chain reaction in murine testes treated with busulphan. Finally, using multiple assays, the functional investigation of MTA1 by its specific knockdown was performed in SC-GC co-cultures.SCs were negatively immunolabeled in the tubules with impaired spermatogenesis. Depletion of murine GCs by treatment with busulphan resulted in a dramatic decrease of the MTA1 transcripts level in the isolated SCs on the 15 th day of treatment and thereafter had totally abolished MTAI expression by the 30th day of treatment, respectively. The addition of isolated round spermatids into SC culture could partially elevate MTAI expression in the latter. Furthermore, MTAI is crucial to maintain the GC nursery function and normal anchoring junction formation in SCs because ablation of MTAI by siRNA induced extensive defects of genes related to SC homeostasis.We propose a novel role for SC-expressing MTAI, which is determined by the presence of surrounding GCs, in mediating the crosstalk between SCs and GCs by influencing a broad spectrum of gene changes.
机译:研究转移相关蛋白1(MTA1)在支持细胞(SCs)中的正常表达是否与邻近的生殖细胞(OCs)相关联,并提供MTA1在该体细胞中的功能相关性。使用免疫组织化学确定受损人类精子发生的SC。使用逆转录酶聚合酶链反应在busulphan处理的小鼠睾丸中评估了GC耗竭对分离的SC中MTA1表达的影响。最后,使用多种测定方法,在SC-GC共培养物中通过MTA1的特异性敲除对MTA1进行功能研究.SCs在肾小管中被阴性免疫标记,精子发生受损。在治疗的第15天,用Busulphan处理的小鼠GC耗竭导致MSC1的MTA1转录水平显着下降,此后在治疗的第30天,MTAI的表达完全消失。将分离的圆形精子添加到SC培养物中可以部分提高MTAI在后者中的表达。此外,MTAI对于维持SC的GC育苗功能和正常的锚定连接形成至关重要,因为siRNA切除MTAI会引起与SC稳态相关的基因的广泛缺陷。我们提出了SC表达MTAI的新作用,这由通过影响广泛的基因变化来介导SC和GC之间的串扰,从而存在周围的GC。

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