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Developmental expression of BMP4/ALK3/SMAD5 signaling pathway in the mouse testis: a potential role of BMP4 in spermatogonia differentiation

机译:BMP4 / ALK3 / SMAD5信号通路在小鼠睾丸中的发育表达:BMP4在精原细胞分化中的潜在作用

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摘要

It is well established that the c-kit gene plays an essential role in the proliferation of differentiating spermatogonia in prepuberal mice. However, the mechanisms that regulate the onset of spermatogenesis, i.e. differentiation of spermatogonial stem cells and c-kit expression, are poorly understood. Here we identify a novel signal transduction system in mouse prepuberal testis regulating this developmental event, involving bone morphogenetic protein 4 (BMP4) and its transduction machinery. BMP4 is produced by Sertoli cells very early in the postnatal life and is successively down regulated in peri-puberal Sertoli cells. Its receptor Alk3 and the R-Smad Smad5 are specifically expressed both in proliferating primordial germ cells and in postnatal spermatogonia. BMP4 stimulation of cultured spermatogonia induces Smad4/5 nuclear translocation and the formation of a DNA-binding complex with the transcriptional coactivator p300/CBP. In vitro exposure of undifferentiated spermatogonia to BMP4 exerts both mitogenic and differentiative effects, inducing [3H]thymidine incorporation and Kit expression. As a result of the latter event, Kit-negative spermatogonia acquire sensitivity to Stem Cell Factor.
机译:众所周知,c-kit基因在青春期前小鼠分化性精原细胞的增殖中起着至关重要的作用。然而,对调节精子发生的机制,即精原干细胞的分化和c-kit表达的了解很少。在这里,我们在小鼠青春期前睾丸中识别出一种新的信号转导系统,调节该发育事件,涉及骨形态发生蛋白4(BMP4)及其转导机制。 BMP4在出生后很早就由Sertoli细胞产生,并在青春期前后的Sertoli细胞中被下调。它的受体Alk3和R-Smad Smad5在增殖的原始生殖细胞和出生后的精原细胞中均特异性表达。 BMP4刺激培养的精原细胞会诱导Smad4 / 5核易位,并与转录共激活因子p300 / CBP形成DNA结合复合物。未分化的精原细胞在体外暴露于BMP4会产生有丝分裂和分化作用,诱导[3H]胸苷的掺入和Kit表达。由于后者,Kit阴性的精原细胞获得了对干细胞因子的敏感性。

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