Griffith University, Parklands Drive, Southport, Queensland, Australia.
Centre for Reproductive Health, Hudson Institute of Medical Research, Clayton, Victoria, Australia.
PLoS One. 2023 Sep 1;18(9):e0290846. doi: 10.1371/journal.pone.0290846. eCollection 2023.
Sertoli cells support the development of sperm and the function of various somatic cells in the interstitium between the tubules. Sertoli cells regulate the function of the testicular vasculature and the development and function of the Leydig cells that produce testosterone for fertility and virility. However, the Sertoli cell-derived factors that regulate these cells are largely unknown. To define potential mechanisms by which Sertoli cells could support testicular somatic cell function, we aimed to identify Sertoli cell-enriched proteins in the testicular interstitial fluid (TIF) between the tubules. We previously resolved the proteome of TIF in mice and humans and have shown it to be a rich source of seminiferous tubule-derived proteins. In the current study, we designed bioinformatic strategies to interrogate relevant proteomic and genomic datasets to identify Sertoli cell-enriched proteins in mouse and human TIF. We analysed proteins in mouse TIF that were significantly reduced after one week of acute Sertoli cell ablation in vivo and validated which of these are likely to arise primarily from Sertoli cells based on relevant mouse testis RNASeq datasets. We used a different, but complementary, approach to identify Sertoli cell-enriched proteins in human TIF, taking advantage of high-quality human testis genomic, proteomic and immunohistochemical datasets. We identified a total of 47 and 40 Sertoli cell-enriched proteins in mouse and human TIF, respectively, including 15 proteins that are conserved in both species. Proteins with potential roles in angiogenesis, the regulation of Leydig cells or steroidogenesis, and immune cell regulation were identified. The data suggests that some of these proteins are secreted, but that Sertoli cells also deposit specific proteins into TIF via the release of extracellular vesicles. In conclusion, we have identified novel Sertoli cell-enriched proteins in TIF that are candidates for regulating somatic cell-cell communication and testis function.
支持精子发生和管间间质中各种体细胞功能的支持细胞。支持细胞调节睾丸脉管系统的功能以及产生睾酮的莱迪希细胞的发育和功能,而睾酮对于生育力和雄性力是必需的。然而,调节这些细胞的支持细胞衍生因子在很大程度上是未知的。为了确定支持细胞支持睾丸体细胞功能的潜在机制,我们旨在鉴定管间睾丸间质液(TIF)中富含支持细胞的蛋白质。我们之前已经解析了小鼠和人类的 TIF 蛋白质组,并表明它是生精小管衍生蛋白质的丰富来源。在当前的研究中,我们设计了生物信息学策略来询问相关的蛋白质组学和基因组数据集,以鉴定小鼠和人类 TIF 中富含支持细胞的蛋白质。我们分析了在体内急性支持细胞消融 1 周后明显减少的小鼠 TIF 中的蛋白质,并根据相关的小鼠睾丸 RNA-seq 数据集验证了其中哪些可能主要来源于支持细胞。我们使用了另一种不同但互补的方法来鉴定人类 TIF 中富含支持细胞的蛋白质,利用了高质量的人类睾丸基因组、蛋白质组和免疫组织化学数据集。我们总共鉴定了 47 种和 40 种在小鼠和人类 TIF 中分别富含支持细胞的蛋白质,包括在两种物种中均保守的 15 种蛋白质。鉴定出了具有潜在作用的蛋白质,包括血管生成、莱迪希细胞或类固醇生成的调节以及免疫细胞调节。数据表明,其中一些蛋白质是分泌性的,但支持细胞也通过释放细胞外囊泡将特定蛋白质沉积到 TIF 中。总之,我们已经在 TIF 中鉴定出了新的富含支持细胞的蛋白质,它们是调节体细胞细胞通讯和睾丸功能的候选物。