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Stra8 和 Tcerg1l 在视黄酸诱导的小鼠精原细胞分化中的作用†。

Roles of Stra8 and Tcerg1l in retinoic acid induced spermatogonial differentiation in mouse†.

机构信息

Department of Biomedical Sciences, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Department of Genetics and Penn Genomics Analysis Core, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Biol Reprod. 2021 Aug 3;105(2):503-518. doi: 10.1093/biolre/ioab093.

Abstract

Retinoic acid (RA) induces spermatogonial differentiation, but the mechanism by which it operates remains largely unknown. We developed a germ cell culture assay system to study genes involved in spermatogonial differentiation triggered by RA. Stimulated by RA 8 (Stra8), a RA-inducible gene, is indispensable for meiosis initiation, and its deletion results in a complete block of spermatogenesis at the pre-leptotene/zygotene stage. To interrogate the role of Stra8 in RA mediated differentiation of spermatogonia, we derived germ cell cultures from the neonatal testis of both wild type and Stra8 knock-out mice. We provide the first evidence that Stra8 plays a crucial role in modulating the responsiveness of undifferentiated spermatogonia to RA and facilitates transition to a differentiated state. Stra8-mediated differentiation is achieved through the downregulation of a large portfolio of genes and pathways, most notably including genes involved in the spermatogonial stem cell self-renewal process. We also report here for the first time the role of transcription elongation regulator-1 like (Tcerg1l) as a downstream effector of RA-induced spermatogonial differentiation.

摘要

维甲酸(RA)诱导精原细胞分化,但它的作用机制在很大程度上仍然未知。我们开发了一种生殖细胞培养测定系统,以研究 RA 诱导的精原细胞分化所涉及的基因。RA 诱导基因 Stra8 刺激对于起始减数分裂是必不可少的,其缺失导致精原细胞在早细线期/合线期完全阻滞。为了研究 Stra8 在 RA 介导的精原细胞分化中的作用,我们从小鼠的新生睾丸中分离出了野生型和 Stra8 敲除型的生殖细胞培养物。我们首次提供了证据表明 Stra8 在调节未分化精原细胞对 RA 的反应性以及促进向分化状态过渡方面起着关键作用。Stra8 介导的分化是通过下调一组大量的基因和途径来实现的,其中最显著的是包括参与精原干细胞自我更新过程的基因。我们还首次报道了转录延伸调节因子 1 样(Tcerg1l)作为 RA 诱导的精原细胞分化的下游效应物的作用。

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