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Peritubular cells of the human testis: prostaglandin E 2 and more
Author(s) -
Mayerhofer Artur
Publication year - 2020
Publication title -
andrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.947
H-Index - 43
eISSN - 2047-2927
pISSN - 2047-2919
DOI - 10.1111/andr.12669
Subject(s) - glial cell line derived neurotrophic factor , biology , medicine , endocrinology , microbiology and biotechnology , receptor , peritubular capillaries , spermatogenesis , neurotrophic factors , kidney
Background Several layers of slender, smooth muscle‐like, peritubular cells and extracellular matrix ( ECM ) form the peritubular compartment of the human testis. Peritubular cells are the least explored testicular cells. Materials and methods Human testicular peritubular cells ( HTPC s) can be isolated from small testicular fragments of patients and studied in vitro. We have used this cellular model, in combination with human testicular samples, to examine how peritubular cells may contribute to male (in)fertility. Results Human testicular peritubular cells (HTPCs) retain contractile abilities in vitro and secrete many proteins. Among them are factors, which serve intra‐testicular roles, for example, glial cell line‐derived neurotrophic factor ( GDNF ), thought to be important for the renewal of spermatogonial stem cells ( SSC s). Studies in mutant mice indicated that peritubular cell‐derived GDNF is crucial for lifelong spermatogenesis. Thus, peritubular cells are a functional part of the SSC niche. Peritubular cells of mice and men express androgen receptors ( AR ). In mouse peritubular cells, androgens enhanced GDNF production, but not in HTPC s. Rather, AR activation increased the levels of AR and smooth muscle proteins and thereby enhanced the smooth muscle‐like phenotype. Following the lead of a proteomic analysis, which identified the key prostaglandin ( PG )‐synthesizing enzyme ( PTGS 1 = COX 1), we found that HTPC s secrete PGE 2 . COX 1, and PGE 2 receptors ( EP 1, 2, and 4) were identified in peritubular cells in situ, supporting in vivo relevance. In HTPC s, activation of EP 1/4 increased GDNF and a smooth muscle protein. Ibuprofen is a nonsteroidal anti‐inflammatory drug ( NSAID ), which blocks PG synthesis. Added to HTPC s it reduced PGE 2 and GDNF production and lowered smooth muscle protein levels. If applicable to the in vivo situation, the results suggest that ibuprofen and possibly other NSAID s may impair important peritubular cell functions and consequently testicular functions. Conclusion The few examples highlighted, together with others not mentioned here, indicate that HTPC s provide an experimental window into the human testis.