CITED2 Binding to EP300 Regulates Human Spermatogonial Stem Cell Proliferation and Survival Through HSPA6.

IF 3.8 3区 医学 Q2 CELL & TISSUE ENGINEERING
Stem Cells International Pub Date : 2025-04-24 eCollection Date: 2025-01-01 DOI:10.1155/sci/2362489
Yongzhe Chen, Bang Liu, Sisi Tao, Lvjun Liu, Jianxin Gao, Ying Liang, Weilei Dong, Dai Zhou
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引用次数: 0

Abstract

Spermatogonial stem cells (SSCs) are essential for the initiation and continuation of spermatogenesis, a process fundamental to male fertility. Despite extensive studies on mouse SSCs, the mechanisms governing self-renewal and differentiation in human SSCs remain to be elucidated. This study investigated the regulatory mechanisms of SSCs by analyzing single-cell sequencing data from the GEO dataset of human testis. Analysis revealed dominant expression of CITED2 in human SSCs. Reduction of CITED2 levels in hSSC lines significantly inhibited proliferation and increased apoptosis. Protein interaction prediction and immunoprecipitation identified interactions between CITED2 and EP300 in SSC lines. RNA sequencing results indicated that CITED2 knockdown significantly affected the MAPK pathway and the HSPA6 gene. Overexpression of HSPA6 mitigated the proliferative and apoptotic changes provoked by CITED2 downregulation. These findings provide novel insights into the regulatory and functional mechanisms of CITED2-mediated hSSC development.

CITED2结合EP300通过HSPA6调控人精原干细胞增殖和存活
精原干细胞(ssc)是精子发生的起始和延续所必需的,精子发生是男性生育的基本过程。尽管对小鼠ssc进行了广泛的研究,但人类ssc自我更新和分化的机制仍有待阐明。本研究通过分析人类睾丸GEO数据集的单细胞测序数据,探讨了ssc的调控机制。分析显示,CITED2在人ssc中占主导地位。降低CITED2水平可显著抑制hSSC细胞增殖,增加细胞凋亡。蛋白相互作用预测和免疫沉淀鉴定了SSC细胞系中CITED2和EP300之间的相互作用。RNA测序结果显示,CITED2敲低显著影响MAPK通路和HSPA6基因。过表达HSPA6可减轻CITED2下调引起的增殖和凋亡变化。这些发现为cited2介导的hSSC发育的调控和功能机制提供了新的见解。
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来源期刊
Stem Cells International
Stem Cells International CELL & TISSUE ENGINEERING-
CiteScore
8.10
自引率
2.30%
发文量
188
审稿时长
18 weeks
期刊介绍: Stem Cells International is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of stem cell biology and applications. The journal will consider basic, translational, and clinical research, including animal models and clinical trials. Topics covered include, but are not limited to: embryonic stem cells; induced pluripotent stem cells; tissue-specific stem cells; stem cell differentiation; genetics and epigenetics; cancer stem cells; stem cell technologies; ethical, legal, and social issues.
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