Huang Yanping, Li Xiangping, Sun Xiangzhou, Yao Jiahui, Gao Fengxin, Wang Zhenqing, Hu Jiaying, Wang Zhu, Ouyang Bin, Tu Xiangan, Zou Xuenong, Liu Wei, Lu Mujun, Deng Chunhua, Yang Qiyun, Xie Yun
Department of Urology and Andrology, Renji Hospital, School of Medicine, Shanghai Institute of Andrology, Shanghai Jiao Tong University, Shanghai, China.
Department of Urology and Andrology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Front Cell Dev Biol. 2022 Feb 8;9:782824. doi: 10.3389/fcell.2021.782824. eCollection 2021.
The elderly males undergo degenerative fertility and testicular endocrine function that jeopardize the reproductive health and well-being. However, the mechanisms underlying reproductive aging are unclear. Here, we tried to address this by investigating the phenotypes and transcriptomes of seven regions of the male mouse reproductive tract: the testis, efferent ductules, initial segment, caput, corpus and cauda epididymidis, and vas deferens, in adult (3 months) and aged (21 months) mice. Quantitative PCR, immunohistochemistry, immunofluorescent staining, and enzyme-linked immunosorbent assay were performed for the analysis of gene expression in mice, human tissues, and semen samples. Aged male mice showed both systematic and reproductive changes, and remarkable histological changes were detected in the testis and proximal epididymis. Transcriptomes of the male reproductive tract were mapped, and a series of region-specific genes were identified and validated in mouse and/or human tissues, including Protamine 1 (), ADAM metallopeptidase domain 28 (), Ribonuclease A family member 13 (), WAP four-disulfide core domain 13 (), and . Meanwhile, age-related transcriptome changes of different regions of the male reproductive tract were characterized. Notably, increased immune response was functionally related to the male reproductive aging, especially the T cell activation. An immune response-associated factor, phospholipase A2 group IID (), was identified as a potential biomarker for reproductive aging in mice. And the PLA2G2D level in human seminal plasma surged at approximately 35 years of age. Furthermore, we highlighted Protein tyrosine phosphatase receptor type C (), Lymphocyte protein tyrosine kinase (), Microtubule associated protein tau (), and Interferon induced protein with tetratricopeptide repeats 3 () as critical molecules in the aging of initial segment, caput, caput, and cauda epididymidis, respectively. This study provides an RNA-seq resource for the male reproductive system during aging in mice, and is expected to improve our understanding of male reproductive aging and infertility.
老年男性会经历生育能力和睾丸内分泌功能的衰退,这会危及生殖健康和福祉。然而,生殖衰老背后的机制尚不清楚。在这里,我们试图通过研究成年(3个月)和老年(21个月)雄性小鼠生殖 tract 的七个区域:睾丸、输出小管、起始段、附睾头、附睾体、附睾尾和输精管的表型和转录组来解决这个问题。进行了定量PCR、免疫组织化学、免疫荧光染色和酶联免疫吸附测定,以分析小鼠、人体组织和精液样本中的基因表达。老年雄性小鼠表现出全身和生殖方面的变化,并且在睾丸和附睾近端检测到明显的组织学变化。绘制了雄性生殖道的转录组图谱,并在小鼠和/或人体组织中鉴定并验证了一系列区域特异性基因,包括鱼精蛋白1()、ADAM金属肽酶结构域28()、核糖核酸酶A家族成员13()、WAP四硫核心结构域13()和。同时,对雄性生殖道不同区域与年龄相关的转录组变化进行了表征。值得注意的是,免疫反应增强在功能上与雄性生殖衰老相关,尤其是T细胞活化。一种免疫反应相关因子,磷脂酶A2组IID(),被确定为小鼠生殖衰老的潜在生物标志物。并且人类精浆中PLA2G2D水平在大约35岁时激增。此外,我们分别强调蛋白酪氨酸磷酸酶受体C型()、淋巴细胞蛋白酪氨酸激酶()、微管相关蛋白tau()和干扰素诱导的含四肽重复序列3的蛋白()是附睾起始段、附睾头、附睾体和附睾尾衰老过程中的关键分子。这项研究为小鼠衰老过程中的雄性生殖系统提供了一个RNA测序资源,有望增进我们对雄性生殖衰老和不育的理解。