Sertoli cell-enriched proteins in mouse and human testicular interstitial fluid

• Published in: PloS one Vol. 18; no. 9; p. e0290846
• Main Authors: O'Donnell, Liza, Dagley, Laura F, Curley, Michael, Darbey, Annalucia, O'Shaughnessy, Peter J, Diemer, Thorsten, Pilatz, Adrian, Fietz, Daniela, Stanton, Peter G, Smith, Lee B, Rebourcet, Diane
• Format: Journal Article
• Language: English
• Published: San Francisco Public Library of Science 01.09.2023; Public Library of Science (PLoS)
• Subjects: Ablation; Analysis; Angiogenesis; Biology and Life Sciences; Cell interactions; Datasets; Engineering and Technology; Enrichment; Fertility; Genomics; Genotype & phenotype; Immune system; Leydig cells; Mass spectrometry; Medicine and Health Sciences; Peptides; Proteins; Proteomes; Proteomics; Research and Analysis Methods; Scientific imaging; Seminiferous tubule; Sertoli cells; Somatic cells; Sperm; Spermatogenesis; Steroidogenesis; Testes; Testosterone; Tubules; Australia
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0290846

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.