CARF promotes spermatogonial self-renewal and proliferation through Wnt signaling pathway

被引:0
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作者
Wenhao Cui
Xiaoli He
Xiaohong Zhai
Huan Zhang
Yuanwei Zhang
Fei Jin
Xiaomin Song
Dianqing Wu
Qinghua Shi
Lin Li
机构
[1] Shanghai Institute of Biochemistry and Cell Biology,State Key Laboratory of Molecular Biology, CAS Center for Excellence in Molecular Cell Science
[2] Chinese Academy of Sciences,School of Life Science and Technology
[3] University of Chinese Academy of Sciences,School of Life Sciences
[4] Shanghai Tech University,Vascular Biology and Therapeutic Program and Department of Pharmacology
[5] University of Science and Technology of China,School of Life Science, Hangzhou Institute for Advanced Study
[6] Yale School of Medicine,undefined
[7] University of Chinese Academy of Sciences,undefined
来源
Cell Discovery | / 6卷
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摘要
Collaborator of ARF (CARF) regulates cell proliferative fate through both p53-dependent and -independent mechanisms. Recently, we reported a new function of CARF as a positive regulator of Wnt signaling. Despite these findings, the physiological function of CARF has not been well studied. Here, we generated CARF knockout mice and found that male CARF−/− mice exhibited significantly impaired fertility and Sertoli-cell-only (SCO) syndrome phenotypes. Further studies revealed that loss of CARF in Sertoli cells led to decreased GDNF expression, which hindered spermatogonial stem cells (SSCs) self-renewal. Meanwhile, CARF loss in undifferentiated spermatogonia impaired their proliferation. These two mechanisms together led to SCO syndrome phenotypes, which could be functionally rescued by pharmacological or genetic reactivation of Wnt signaling. Finally, we identified CARFS351F as a potential pathogenic mutation in an SCO patient. Overall, our findings reveal important roles of CARF in spermatogonial self-renewal and proliferation through the Wnt signaling pathway.
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