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NANOS2 acts as an intrinsic regulator of gonocytes-to-spermatogonia transition in the murine testes

机译:纳米纳米用作鼠睾丸中的京氏腺细胞对精子转变的内在调节剂

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In the male mouse embryos, the primordial germ cells colonize the developing testes at E11.5. These resident germ cells termed gonocytes are the predecessors of spermatogonial stem cells ( SSCs) and differentiating spermatogonia. Both of which are essential for male fertility where the former maintains the continuity of spermatogenesis and the latter generates pioneering waves of spermatozoa. Therefore the timely initiation of gonocytes-to- spermatogonia transition ( GST) is an important process during which the cell fates of gonocytes-might be segregated. However, it is unknown whether gonocytes are composed of a heterogeneous mixture of germ cells with distinct differentiation potentials during GST. Here, we find that gonocytes exhibit heterogeneity in terms of the expression pattern of at least three early spermatogonial marker genes namely Nanos2, Stra8 and Gfra1. NANOS2 expression levels are negatively correlated with those of STRA8 and GFRA1 before GST, while positive correlation with GFRA1 is established after GST. We further find that overexpression of NANOS2 results in the repression of GFRA1 and PLZF in gonocytes, leading to a delay in GST. On the other hand, loss of NANOS2 results in the up-regulation of GFRA1 and PLZF, indicating a precocious entry of GST. Taken together, our data suggest that NANOS2 functions as an intrinsic timekeeper of GST in the mouse testes. (C) 2018 Elsevier B.V. All rights reserved.
机译:在雄性小鼠胚胎中,原始胚芽细胞在E11.5处定植显影睾丸。这些驻留的腺细胞称为腺细胞是精牙科干细胞(SSCs)和分化精子的前任。这两者对于前者保持精子发生的连续性并且后者产生了精子的开创性波浪,这两者都是必不可少的。因此,及时引发腺细胞 - 精子转变(GST)是一个重要的过程,在此期间淋可序列的腺细胞的束缚。然而,尚不清楚gonocytes是否由GST在GST期间具有不同分化电位的生殖细胞的异质混合物组成。在这里,我们发现淋病细胞在至少三种早期精术标志物基因的表达模式中表现出异质性,即纳米2,STRA8和GFRA1。在GST之前,纳米2表达水平与STRA8和GFRA1的表达水平负相关,而GST之后建立与GFRA1的正相关。我们进一步发现纳米2的过度表达导致淋病中的GFRA1和PLZF的抑制,导致GST的延迟。另一方面,纳米2的丧失导致GFRA1和PLZF的上调,表明GST的早熟。我们的数据结合在一起,建议纳米纳米在鼠标睾丸中作为GST的内在计时器。 (c)2018 Elsevier B.v.保留所有权利。

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