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Spermatogonial stem cell quest: nanos2, marker of a sub-population of undifferentiated A spermatogonia in trout testis

机译:精原干细胞探索:nanos2,鳟鱼睾丸中未分化的精子亚群的标记

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摘要

Continuous or cyclic production of spermatozoa throughout life in adult male vertebrate depends on a sub-population of undifferentiated germ cells acting as spermatogonial stem cells (SSCs). What makes these cells self-renew or differentiate is barely understood, in particular in non-mammalian species including fish. In the highly seasonal rainbow trout, at the end of the annual spermatogenetic cycle, tubules of the spawning testis contain only spermatozoa with the exception of scarce undifferentiated spermatogonia that remain on the tubular wall, which will support the next round of spermatogenesis. Taking advantage of this model, we identified putative SSCs in fish testis using morphological, molecular and functional approaches. In all stages, large spermatogonia with ultrastructural characteristics of germinal stem cells were found, isolated or in doublet. Trout homologs of SSC and/or immature progenitor markers in mammals, nanos2 and nanos3, pou2, plzf and piwil2, were preferentially expressed in the prepubertal testis and in the undifferentiated A spermatogonia populations purified by centrifugal elutriation. This expression profile strongly suggests that these genes are functionally conserved between fish and mammals. Moreover, transplantation into embryonic recipients of the undifferentiated spermatogonial cells demonstrated their high 'stemness' efficiency in terms of migration into gonads and ability to give functional gametes. Interestingly, we show that nanos2 expression was restricted to a sub-population of undifferentiated spermatogonia (less than 20%) present as isolated cells or in doublet in the juvenile and in the maturing trout testis. In contrast, nanos2 transcript was detected in all the undifferentiated spermatogonia remaining in the spawning testis. Plzf was also immuno-detected in A-Spg from spawning testis, which reinforces the idea that these cells are stem cells. From those results, we hypothesize that the subset of undifferentiated A spermatogonia expressing nanos2 transcript are putative SSC in trout.
机译:成年雄性脊椎动物终生持续或循环产生精子,取决于未分化生殖细胞的亚群,这些未分化生殖细胞充当精原干细胞(SSC)。使得这些细胞自我更新或分化的原因鲜为人知,特别是在包括鱼类在内的非哺乳动物物种中。在高度季节性的虹鳟鱼中,在每年的精子形成周期结束时,产卵睾丸的小管仅包含精子,但保留在肾小管壁上的稀有未分化精子除外,这将支持下一轮精子发生。利用该模型,我们使用形态学,分子学和功能学方法在鱼睾丸中鉴定出推定的SSC。在所有阶段,发现,分离或成对存在具有生胚干细胞超微结构特征的大型精原细胞。在哺乳动物,nanos2和nanos3,pou2,plzf和piwil2中,SSC和/或未成熟祖细胞标记的鳟鱼同源物优先在青春期前的睾丸和通过离心淘析纯化的未分化A精原细胞群体中表达。该表达谱强烈暗示这些基因在鱼类和哺乳动物之间在功能上是保守的。此外,将其移植到未分化的精原细胞的胚胎受体中,证明它们在迁移到性腺中和提供功能性配子的能力方面具有很高的“干性”效率。有趣的是,我们显示了nanos2的表达仅限于未分化的精原细胞亚群(少于20%),这些精原细胞以分离的细胞形式存在,或者在少年和成年鳟鱼的睾丸中以双重形式存在。相反,在产卵睾丸中残留的所有未分化的精原细胞中均检测到了nanos2转录本。还从产卵睾丸的A-Spg中免疫检测到Plzf,这强化了这些细胞是干细胞的观念。根据这些结果,我们假设未分化的精原细胞表达nanos2转录本的子集是鳟鱼中的假定SSC。

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