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鉴定CHD1L作为精原干细胞存活和自我更新的重要调节因子。

Identification of CHD1L as an Important Regulator for Spermatogonial Stem Cell Survival and Self-Renewal.

作者信息

Liu Shan-Shan, Bai Yin-Shan, Feng Li, Dong Wen-Wei, Li Yang, Xu Li-Ping, Ma Ning-Fang

机构信息

Department of Histology and Embryology, Guangzhou Medical University, Guangzhou, China.

出版信息

Stem Cells Int. 2016;2016:4069543. doi: 10.1155/2016/4069543. Epub 2016 Nov 27.

Abstract

Chromodomain helicase/ATPase DNA binding protein 1-like gene () participates in chromatin-dependent processes, including transcriptional activation and DNA repair. In this study, we have found for the first time that Chd1l is mainly expressed in the testicular tissues of prepubertal and adult mice and colocalized with PLZF, OCT4, and GFR1 in the neonatal mouse testis and THY1 undifferentiated spermatogonia or spermatogonial stem cells (SSCs). Knockdown of endogenous in cultured mouse undifferentiated SSCs inhibited the expression levels of , , , and genes, suppressed SSC colony formation, and reduced BrdU incorporation, while increasing SSC apoptosis. Moreover, the gene expression is activated by GDNF in the cultured mouse SSCs, and the GDNF signaling pathway was modulated by endogenous levels of Chd1l; as demonstrated by the gene expression levels of GDNF, inducible transcripts , , , and , but not that of GDNF-independent gene, , were significantly downregulated by Chd1l knockdown in mouse SSCs. Taken together, this study provides the first evidence to support the notion that is an intrinsic and novel regulator for SSC survival and self-renewal, and it exerts such regulation at least partially through a GDNF signaling pathway.

摘要

染色质结构域解旋酶/ATP酶DNA结合蛋白1样基因()参与依赖染色质的过程,包括转录激活和DNA修复。在本研究中,我们首次发现Chd1l主要在青春期前和成年小鼠的睾丸组织中表达,并在新生小鼠睾丸以及THY1未分化精原细胞或精原干细胞(SSCs)中与PLZF、OCT4和GFR1共定位。在培养的小鼠未分化SSCs中敲低内源性会抑制、、和基因的表达水平,抑制SSC集落形成,并减少BrdU掺入,同时增加SSC凋亡。此外,在培养的小鼠SSCs中,GDNF可激活基因表达,且GDNF信号通路受Chd1l内源性水平的调节;如GDNF、诱导转录本、、和的基因表达水平所示,但不依赖GDNF的基因的表达水平在小鼠SSCs中不受Chd1l敲低的显著下调。综上所述,本研究提供了首个证据支持是SSC存活和自我更新的内在新型调节因子这一观点,且它至少部分通过GDNF信号通路发挥这种调节作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c333/5149700/7e17f3decc0c/SCI2016-4069543.001.jpg

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