Department of Physiology, Michigan State University, East Lansing, Michigan, 48824, USA.
Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan, 48824, USA.
Sci Rep. 2019 Oct 29;9(1):15525. doi: 10.1038/s41598-019-52105-9.
Male infertility might be caused by genetic and/or environmental factors that impair spermatogenesis and epididymal sperm maturation. Here we report that heterozygous deletion of the nuclear receptor coactivator-5 (Ncoa5) gene resulted in decreased motility and progression of spermatozoa in the cauda epididymis, leading to infertility in male mice. Light microscopic and ultrastructural analysis revealed morphological defects in the spermatozoa collected from the cauda epididymis of Ncoa5 mice. Immunohistochemistry showed that interleukin-6 (IL-6) expression in epithelial cells of Ncoa5 epididymis was higher than wild type counterparts. Furthermore, heterozygous deletion of Il-6 gene in Ncoa5 male mice partially improved spermatozoa motility and moderately rescued infertility phenotype. Our results uncover a previously unknown physiological role of NCOA5 in the regulation of epididymal sperm maturation and suggest that NCOA5 deficiency could cause male infertility through increased IL-6 expression in epididymis.
男性不育可能是由遗传和/或环境因素引起的,这些因素会损害精子发生和附睾精子成熟。在这里,我们报告说,核受体共激活因子 5(Ncoa5)基因的杂合缺失导致精子在附睾尾部的运动和进展减少,导致雄性小鼠不育。光镜和超微结构分析显示,从 Ncoa5 小鼠附睾尾部收集的精子存在形态缺陷。免疫组织化学显示,Ncoa5 附睾上皮细胞中白细胞介素 6(IL-6)的表达高于野生型对照。此外,Ncoa5 雄性小鼠中 Il-6 基因的杂合缺失部分改善了精子的运动能力,并适度挽救了不育表型。我们的结果揭示了 NCOA5 在调节附睾精子成熟中的一个以前未知的生理作用,并表明 NCOA5 缺乏可能通过增加附睾中 IL-6 的表达导致男性不育。