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酪蛋白激酶1α调节成年小鼠的睾酮合成和睾丸发育。

Casein Kinase 1α Regulates Testosterone Synthesis and Testis Development in Adult Mice.

作者信息

Guo Hongzhou, Zhang Di, Zhou Yewen, Sun Longjie, Li Changping, Luo Xuan, Liu Jiali, Cui Sheng

机构信息

College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, Jiangsu, People's Republic of China.

State Key Laboratory of Farm Animal Biotech Breeding, College of Biological Sciences, China Agricultural University, Beijing 10021, People's Republic of China.

出版信息

Endocrinology. 2023 Mar 13;164(5). doi: 10.1210/endocr/bqad042.

Abstract

Casein kinase 1α (CK1α) is a main component of the Wnt/β-catenin signaling pathway, which participates in multiple biological processes. Our recent study demonstrated that CK1α is expressed in both germ cells and somatic cells of mouse testes and regulates spermatogenesis. However, little information is known about the role of CK1α in regulating the development of somatic cells in mouse testes. Our results demonstrated that conditional disruption of CK1α in murine Leydig cells sharply decreased testosterone levels; markedly affected testis development, sperm motility, and sperm morphology; and caused subfertility. The germ cell population was partially decreased in CK1α conditional knockout (cKO) mice, while the proliferation of Leydig cells and Sertoli cells was not affected. Furthermore, in vitro results verified that luteinizing hormone upregulates CK1α through the luteinizing hormone/protein kinase/Epidermal Growth Factor Receptor/extracellular regulated protein kinases/2 signaling pathway and that CK1α interacts with and phosphorylates EGFR, which subsequently activates the phosphorylation of ERK1/2, thereby promoting testosterone synthesis. In addition, high-dose testosterone propionate partially rescued the phenotype observed in cKO mice. This study provides new insights into the role of CK1α in steroidogenesis and male reproduction.

摘要

酪蛋白激酶1α(CK1α)是Wnt/β-连环蛋白信号通路的主要组成部分,参与多种生物学过程。我们最近的研究表明,CK1α在小鼠睾丸的生殖细胞和体细胞中均有表达,并调节精子发生。然而,关于CK1α在调节小鼠睾丸体细胞发育中的作用,目前所知甚少。我们的结果表明,小鼠睾丸间质细胞中CK1α的条件性缺失会显著降低睾酮水平;明显影响睾丸发育、精子活力和精子形态,并导致生育力下降。在CK1α条件性敲除(cKO)小鼠中,生殖细胞数量部分减少,而睾丸间质细胞和支持细胞的增殖未受影响。此外,体外实验结果证实,促黄体生成素通过促黄体生成素/蛋白激酶/表皮生长因子受体/细胞外调节蛋白激酶/2信号通路上调CK1α,且CK1α与表皮生长因子受体相互作用并使其磷酸化,进而激活细胞外信号调节激酶1/2的磷酸化,从而促进睾酮合成。此外,高剂量丙酸睾酮部分挽救了在cKO小鼠中观察到的表型。本研究为CK1α在类固醇生成和雄性生殖中的作用提供了新的见解。

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