Heinrich A, DeFalco T
Division of Reproductive Sciences, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, MLC 7045, Cincinnati, OH, 45229, USA.
Department of Pediatrics, University of Cincinnati College of Medicine, 3230 Eden Avenue, Suite E-870, Cincinnati, OH, 45267, USA.
Andrology. 2020 Jul;8(4):903-914. doi: 10.1111/andr.12703. Epub 2019 Sep 30.
Testicular architecture and sperm production are supported by a complex network of communication between various cell types. These signals ensure fertility by: regulating spermatogonial stem/progenitor cells; promoting steroidogenesis; and driving male-specific differentiation of the gonad. Sertoli cells have long been assumed to be the major cellular player in testis organogenesis and spermatogenesis. However, cells in the interstitial compartment, such as Leydig, vascular, immune, and peritubular cells, also play prominent roles in the testis but are less well understood.
Here, we aim to outline our current knowledge of the cellular and molecular mechanisms by which interstitial cell types contribute to spermatogenesis and testicular development, and how these diverse constituents of the testis play essential roles in ensuring male sexual differentiation and fertility.
We surveyed scientific literature and summarized findings in the field that address how interstitial cells interact with other interstitial cell populations and seminiferous tubules (i.e., Sertoli and germ cells) to support spermatogenesis, male-specific differentiation, and testicular function. These studies focused on 4 major cell types: Leydig cells, vascular cells, immune cells, and peritubular cells.
A growing number of studies have demonstrated that interstitial cells play a wide range of functions in the fetal and adult testis. Leydig cells, through secretion of hormones and growth factors, are responsible for steroidogenesis and progression of spermatogenesis. Vascular, immune, and peritubular cells, apart from their traditionally acknowledged physiological roles, have a broader importance than previously appreciated and are emerging as essential players in stem/progenitor cell biology.
Interstitial cells take part in complex signaling interactions with both interstitial and tubular cell populations, which are required for several biological processes, such as steroidogenesis, Sertoli cell function, spermatogenesis, and immune regulation. These various processes are essential for testicular function and demonstrate how interstitial cells are indispensable for male fertility.
睾丸结构和精子生成由多种细胞类型之间复杂的通讯网络所支持。这些信号通过以下方式确保生育能力:调节精原干细胞/祖细胞;促进类固醇生成;驱动性腺的雄性特异性分化。长期以来,支持细胞一直被认为是睾丸器官发生和精子发生中的主要细胞参与者。然而,间质区室中的细胞,如睾丸间质细胞、血管细胞、免疫细胞和睾丸周细胞,在睾丸中也发挥着重要作用,但人们对它们的了解较少。
在此,我们旨在概述目前关于间质细胞类型促进精子发生和睾丸发育的细胞和分子机制的知识,以及睾丸的这些不同组成部分如何在确保男性性分化和生育能力方面发挥重要作用。
我们查阅了科学文献,并总结了该领域中关于间质细胞如何与其他间质细胞群体和生精小管(即支持细胞和生殖细胞)相互作用以支持精子发生、雄性特异性分化和睾丸功能的研究结果。这些研究聚焦于4种主要细胞类型:睾丸间质细胞、血管细胞、免疫细胞和睾丸周细胞。
越来越多的研究表明,间质细胞在胎儿和成年睾丸中发挥着广泛的功能。睾丸间质细胞通过分泌激素和生长因子,负责类固醇生成和精子发生的进展。血管细胞、免疫细胞和睾丸周细胞,除了其传统上公认的生理作用外,具有比以前认识到的更广泛的重要性,并且正在成为干细胞/祖细胞生物学中的关键参与者。
间质细胞参与了与间质和小管细胞群体的复杂信号相互作用,这是类固醇生成、支持细胞功能、精子发生和免疫调节等多种生物学过程所必需的。这些不同的过程对于睾丸功能至关重要,并证明了间质细胞对于男性生育能力是不可或缺的。