Potter Sarah J, DeFalco Tony
Division of Reproductive SciencesCincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Division of Reproductive SciencesCincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA
Reproduction. 2017 Apr;153(4):R151-R162. doi: 10.1530/REP-16-0588. Epub 2017 Jan 23.
Intricate cellular and molecular interactions ensure that spermatogonial stem cells (SSCs) proceed in a step-wise differentiation process through spermatogenesis and spermiogenesis to produce sperm. SSCs lie within the seminiferous tubule compartment, which provides a nurturing environment for the development of sperm. Cells outside of the tubules, such as interstitial and peritubular cells, also help direct SSC activity. This review focuses on interstitial (interstitial macrophages, Leydig cells and vasculature) and peritubular (peritubular macrophages and peritubular myoid cells) cells and their role in regulating the SSC self-renewal and differentiation in mammals. Leydig cells, the major steroidogenic cells in the testis, influence SSCs through secreted factors, such as insulin growth factor 1 (IGF1) and colony-stimulating factor 1 (CSF1). Macrophages interact with SSCs through various potential mechanisms, such as CSF1 and retinoic acid (RA), to induce the proliferation or differentiation of SSCs respectively. Vasculature influences SSC dynamics through CSF1 and vascular endothelial growth factor (VEGF) and by regulating oxygen levels. Lastly, peritubular myoid cells produce one of the most well-known factors that is required for SSC self-renewal, glial cell line-derived neurotrophic factor (GDNF), as well as CSF1. Overall, SSC interactions with interstitial and peritubular cells are critical for SSC function and are an important underlying factor promoting male fertility.
复杂的细胞和分子相互作用确保精原干细胞(SSCs)在精子发生和精子形成过程中逐步进行分化,以产生精子。SSCs位于生精小管区域内,该区域为精子发育提供了滋养环境。小管外的细胞,如间质细胞和管周细胞,也有助于指导SSC的活动。本综述重点关注间质细胞(间质巨噬细胞、睾丸间质细胞和脉管系统)和管周细胞(管周巨噬细胞和管周肌样细胞)及其在调节哺乳动物SSC自我更新和分化中的作用。睾丸间质细胞是睾丸中主要的类固醇生成细胞,通过分泌因子,如胰岛素生长因子1(IGF1)和集落刺激因子1(CSF1)影响SSCs。巨噬细胞通过各种潜在机制与SSCs相互作用,如CSF1和视黄酸(RA),分别诱导SSCs的增殖或分化。脉管系统通过CSF1和血管内皮生长因子(VEGF)以及调节氧水平影响SSC的动态变化。最后,管周肌样细胞产生SSC自我更新所需的最著名因子之一,即胶质细胞系衍生神经营养因子(GDNF)以及CSF1。总体而言,SSC与间质细胞和管周细胞的相互作用对SSC功能至关重要,是促进男性生育能力的重要潜在因素。