Smoothened mediates medaka spermatogonia proliferation via Gli1-Rgcc-Cdk1 axis

被引:1
|
作者
Zhao, Changle [1 ]
Liu, Xiang [1 ]
Liu, Lei [1 ]
Li, Jianeng [1 ]
Liu, Xingyong [1 ]
Tao, Wenjing [1 ]
Wang, Deshou [1 ]
Wei, Jing [1 ]
机构
[1] Southwest Univ, Sch Life Sci,Integrat Sci Ctr Germplasm Creat West, Key Lab Freshwater FishReproduct & Dev Minist Educ, Lab Aquat Sci Chongqing, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金;
关键词
smoothened; Gli1; Rgcc; spermatogonia; proliferation; survival; RESPONSE GENE; COMPLEMENT; 32; UNDIFFERENTIATED SPERMATOGONIA; CELL-CYCLE; RGC-32; EXPRESSION; MAINTENANCE; CYCLOPAMINE; SURVIVAL; REVEALS;
D O I
10.1093/biolre/ioad090
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The proliferation of spermatogonia directly affects spermatogenesis and male fertility, but its underlying molecular mechanisms are poorly understood. In this study, Smoothened (Smo), the central transducer of Hedgehog signaling pathway, was characterized in medaka (Oryzias latipes), and its role and underlying mechanisms in the proliferation of spermatogonia were investigated. Smo was highly expressed in spermatogonia. In ex vivo testicular organ culture and a spermatogonial cell line (SG3) derived from medaka mature testis, Smo activation promoted spermatogonia proliferation, while its inhibition induced apoptosis. The expression of glioma-associated oncogene homolog 1 (gli1) and regulator of cell cycle (rgcc) was significantly upregulated in SG3 after Smo activation. Furthermore, Gli1 transcriptionally upregulated the expression of rgcc, and Rgcc overexpression rescued cell apoptosis caused by Smo or Gli1 inhibition. Co-immunoprecipitation assay indicated that Rgcc could interact with cyclin-dependent kinase 1 (Cdk1) to regulate the cell cycle of spermatogonia. Collectively, our study firstly reveals that Smo mediates the proliferation of spermatogonia through Gli1-Rgcc-Cdk1 axis. In addition, Smo and Gli1 are necessary of the survival of spermatogonia. This study deepens our understanding of spermatogonia proliferation and survival at the molecular level, and provides insights into male fertility control and reproductive disease treatment.
引用
收藏
页码:772 / 784
页数:13
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