ID家族蛋白在精原干细胞中的功能冗余作用

IF 5.9 2区 医学 Q1 CELL & TISSUE ENGINEERING
Hue M La, Ai-Leen Chan, Ashlee M Hutchinson, Bianka Y M Su, Fernando J Rossello, Ralf B Schittenhelm, Robin M Hobbs
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引用次数: 0

摘要

精原干细胞(SSC)对精子的持续生成至关重要,但SSC的调控机制和标志物仍不十分明确。研究表明,Id家族转录调节因子Id4在SSC中表达并参与SSC的维持。在这里,我们使用报告基因和基因敲除模型来确定Id4在成年男性生殖系中的表达和功能。在精原细胞池中,Id4报告基因的表达和DNA结合抑制因子4(ID4)蛋白在整个GFRα1+部分中都能发现,GFRα1+部分是自我更新的群体。然而,成体造血干细胞能耐受Id4缺失,同时还能显示减数分裂精母细胞的作用。Id4缺失后,未分化精原细胞的培养可以建立。重要的是,未分化精原细胞中ID4的缺失会引发ID3的上调,而在野生型细胞中,这两种ID蛋白都与转录因子伙伴TCF3相关联。在培养的精原细胞中联合抑制ID会破坏干细胞状态并阻碍增殖。因此,我们的数据证明了IDs在干细胞功能中的关键但功能冗余的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functionally redundant roles of ID family proteins in spermatogonial stem cells.

Spermatogonial stem cells (SSCs) are essential for sustained sperm production, but SSC regulatory mechanisms and markers remain poorly defined. Studies have suggested that the Id family transcriptional regulator Id4 is expressed in SSCs and involved in SSC maintenance. Here, we used reporter and knockout models to define the expression and function of Id4 in the adult male germline. Within the spermatogonial pool, Id4 reporter expression and inhibitor of DNA-binding 4 (ID4) protein are found throughout the GFRα1+ fraction, comprising the self-renewing population. However, Id4 deletion is tolerated by adult SSCs while revealing roles in meiotic spermatocytes. Cultures of undifferentiated spermatogonia could be established following Id4 deletion. Importantly, ID4 loss in undifferentiated spermatogonia triggers ID3 upregulation, and both ID proteins associate with transcription factor partner TCF3 in wild-type cells. Combined inhibition of IDs in cultured spermatogonia disrupts the stem cell state and blocks proliferation. Our data therefore demonstrate critical but functionally redundant roles of IDs in SSC function.

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来源期刊
Stem Cell Reports
Stem Cell Reports CELL & TISSUE ENGINEERING-CELL BIOLOGY
CiteScore
10.50
自引率
1.70%
发文量
200
审稿时长
28 weeks
期刊介绍: Stem Cell Reports publishes high-quality, peer-reviewed research presenting conceptual or practical advances across the breadth of stem cell research and its applications to medicine. Our particular focus on shorter, single-point articles, timely publication, strong editorial decision-making and scientific input by leaders in the field and a "scoop protection" mechanism are reasons to submit your best papers.
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