School of Molecular Biosciences, Washington State University, Pullman, WA 99164, USA.
Biol Reprod. 2024 Oct 14;111(4):959-974. doi: 10.1093/biolre/ioae115.
Sertoli cells, omnipresent, somatic cells within the seminiferous tubules of the mammalian testis are essential to male fertility. Sertoli cells maintain the integrity of the testicular microenvironment, regulate hormone synthesis, and of particular importance, synthesize the active derivative of vitamin A, all trans retinoic acid (atRA), which is required for germ cell differentiation and the commitment of male germ cells to meiosis. Stages VIII-IX, when atRA synthesis occurs in the testis, coincide with multiple germ cell development and testicular restructuring events that rely on Sertoli cell gene products to proceed normally. In this study, we have synchronized and captured the mouse testis at four recurrent points of atRA synthesis to observe transcriptomic changes within Sertoli cells as mice age and the Sertoli cells are exposed to increasingly developed germ cell subtypes. This work provides comprehensive, high-resolution characterization of the timing of induction of functional Sertoli cell genes across the first wave of spermatogenesis, and outlines in silico predictions of germ cell derived signaling mechanisms targeting Sertoli cells. We have found that Sertoli cells adapt to their environment, especially to the needs of the germ cell populations present and establish germ-Sertoli cell and Sertoli-Sertoli cell junctions early but gain many of their known immune-regulatory and protein secretory functions in preparation for spermiogenesis and spermiation. Additionally, we have found unique patterns of germ-Sertoli signaling present at each endogenous pulse of atRA, suggesting individual functions of the various germ cells in germ-Sertoli communication.
支持细胞是哺乳动物睾丸生精小管中普遍存在的体细胞,对男性生育能力至关重要。支持细胞维持睾丸微环境的完整性,调节激素合成,特别是合成维生素 A 的活性衍生物全反式视黄酸(atRA),这是生殖细胞分化和雄性生殖细胞进入减数分裂所必需的。在生精小管中合成 atRA 的阶段 VIII-IX 与多个生殖细胞发育和睾丸重构事件同时发生,这些事件依赖于支持细胞基因产物的正常进行。在这项研究中,我们对小鼠睾丸进行了同步化处理,并在四个反复出现的 atRA 合成点捕获了小鼠睾丸,以观察随着年龄的增长,以及支持细胞暴露于不断发育的生殖细胞亚型时,支持细胞内的转录组变化。这项工作全面、高分辨率地描述了在第一次精子发生过程中功能性支持细胞基因的诱导时间,并概述了针对支持细胞的生殖细胞衍生信号机制的计算预测。我们发现支持细胞会适应其环境,尤其是适应存在的生殖细胞群体的需求,并在早期建立生殖细胞-支持细胞和支持细胞-支持细胞连接,但为了准备精子发生和精子释放,它们会获得许多已知的免疫调节和蛋白质分泌功能。此外,我们在每个内源 atRA 脉冲中发现了独特的生殖细胞-支持细胞信号模式,这表明各种生殖细胞在生殖细胞-支持细胞通讯中具有不同的功能。