Division of Urology, Department of Surgery, University of Utah School of Medicine, Salt Lake City, UT 84112, USA; Howard Hughes Medical Institute, Department of Oncological Sciences and Huntsman Cancer Institute, University of Utah School of Medicine, Salt Lake City, UT 84112, USA.
Department of Obstetrics, Gynecology and Reproductive Sciences and Magee-Womens Research Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Dev Cell. 2022 May 9;57(9):1160-1176.e5. doi: 10.1016/j.devcel.2022.04.004. Epub 2022 May 2.
Aging men display reduced reproductive health; however, testis aging is poorly understood at the molecular and genomic levels. Here, we utilized single-cell RNA-seq to profile over 44,000 cells from both young and older men and examined age-related changes in germline development and in the testicular somatic cells. Age-related changes in spermatogonial stem cells appeared modest, whereas age-related dysregulation of spermatogenesis and somatic cells ranged from moderate to severe. Altered pathways included signaling and inflammation in multiple cell types, metabolic signaling in Sertoli cells, hedgehog signaling and testosterone production in Leydig cells, cell death and growth in testicular peritubular cells, and possible developmental regression in both Leydig and peritubular cells. Remarkably, the extent of dysregulation correlated with body mass index in older but not in younger men. Collectively, we reveal candidate molecular mechanisms underlying the complex testicular changes conferred by aging and their possible exacerbation by concurrent chronic conditions such as obesity.
男性随着年龄的增长生殖健康状况会下降;然而,睾丸衰老在分子和基因组水平上的机制尚不清楚。在这里,我们利用单细胞 RNA-seq 技术对来自年轻和年老男性的超过 44000 个细胞进行了分析,研究了生殖细胞发育和睾丸体细胞随年龄变化的相关情况。精原干细胞的年龄相关性变化似乎不大,而精子发生和体细胞的年龄相关性失调从中度到重度不等。受影响的途径包括多种细胞类型的信号转导和炎症、支持细胞中的代谢信号转导、Leydig 细胞中的 hedgehog 信号转导和睾酮生成、睾丸小管周围细胞的细胞死亡和生长,以及 Leydig 细胞和小管周围细胞的可能发育退化。值得注意的是,这种失调的程度与肥胖等慢性疾病相关,在年老男性中与体重指数相关,但在年轻男性中则不相关。总的来说,我们揭示了衰老导致的复杂睾丸变化的潜在分子机制,以及肥胖等慢性疾病可能加剧这些变化的机制。