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Hormone induced differential transcriptome analysis of Sertoli cells during postnatal maturation of rat testes

机译:大鼠睾丸产后成熟过程中激素诱导的支持细胞差异转录组分析

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摘要

Sertoli cells (Sc) are unique somatic cells of testis that are the target of both FSH and testosterone (T) and regulate spermatogenesis. Although Sc of neonatal rat testes are exposed to high levels of FSH and T, robust differentiation of spermatogonial cells becomes conspicuous only after 11-days of postnatal age. We have demonstrated earlier that a developmental switch in terms of hormonal responsiveness occurs in rat Sc at around 12 days of postnatal age during the rapid transition of spermatogonia A to B. Therefore, such “functional maturation” of Sc, during pubertal development becomes prerequisite for the onset of spermatogenesis. However, a conspicuous difference in robust hormone (both T and FSH) induced gene expression during the different phases of Sc maturation restricts our understanding about molecular events necessary for the spermatogenic onset and maintenance. Here, using microarray technology, we for the first time have compared the differential transcriptional profile of Sc isolated and cultured from immature (5 days old), maturing (12 days old) and mature (60 days old) rat testes. Our data revealed that immature Sc express genes involved in cellular growth, metabolism, chemokines, cell division, MAPK and Wnt pathways, while mature Sc are more specialized expressing genes involved in glucose metabolism, phagocytosis, insulin signaling and cytoskeleton structuring. Taken together, this differential transcriptome data provide an important resource to reveal the molecular network of Sc maturation which is necessary to govern male germ cell differentiation, hence, will improve our current understanding of the etiology of some forms of idiopathic male infertility.
机译:睾丸支持细胞(Sc)是睾丸独特的体细胞,是FSH和睾丸激素(T)的靶标,并调节精子发生。尽管新生大鼠睾丸的Sc暴露于高水平的FSH和T,但精子角质细胞的强大分化仅在出生后11天后才明显。先前我们已经证明,在精子A到B的快速过渡过程中,鼠Sc在出生后12天左右发生激素反应方面的发育转换。因此,青春期发育过程中Sc的这种“功能成熟”成为精子发生的开始。然而,在Sc成熟的不同阶段,健壮激素(T和FSH)诱导的基因表达存在明显差异,这限制了我们对生精发作和维持所必需的分子事件的理解。在这里,我们使用微阵列技术首次比较了从未成熟(5天大),成熟(12天大)和成熟(60天大)大鼠睾丸中分离和培养的Sc的差异转录谱。我们的数据显示,不成熟的Sc表达基因参与细胞生长,代谢,趋化因子,细胞分裂,MAPK和Wnt途径,而成熟的Sc更专门表达基因,涉及葡萄糖代谢,吞噬作用,胰岛素信号传导和细胞骨架结构。两者合计,这些差异转录组数据提供了重要的资源,以揭示Sc成熟的分子网络,这是控制雄性生殖细胞分化所必需的,因此,将增进我们目前对某些形式的特发性男性不育症的病因学的了解。

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