Autocrine androgen action is essential for Leydig cell maturation and function, and protects against late‐onset Leydig cell apoptosis in both mice and men

• Published in: The FASEB journal 2015-03, Vol.29 (3), p.894-910
• Main Authors: O'Hara, Laura, McInnes, Kerry, Simitsidellis, Ioannis, Morgan, Stephanie, Atanassova, Nina, Slowikowska‐Hilczer, Jolanta, Kula, Krzysztof, Szarras‐Czapnik, Maria, Milne, Laura, Mitchell, Rod T., Smith, Lee B.
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Androgen-Insensitivity Syndrome - drug therapy; Androgen-Insensitivity Syndrome - metabolism; Androgen-Insensitivity Syndrome - pathology; Androgens - pharmacology; Animals; Apoptosis - drug effects; Autocrine Communication; Blotting, Western; Cells, Cultured; Child; estrogen; Humans; Immunoenzyme Techniques; Leydig Cells - drug effects; Leydig Cells - metabolism; Leydig Cells - pathology; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Protective Agents - pharmacology; Real-Time Polymerase Chain Reaction; Receptors, Androgen - physiology; Research Communication; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - genetics; spermatogenesis; Spermatogenesis - drug effects; steroidogenesis; testis; Testis - drug effects; Testis - metabolism; Testis - pathology; testosterone; Young Adult
• ISSN: 0892-6638; 1530-6860
• DOI: 10.1096/fj.14-255729

Leydig cell number and function decline as men age, and low testosterone is associated with all “Western” cardio‐metabolic disorders. However, whether perturbed androgen action within the adult Leydig cell lineage predisposes individuals to this late‐onset degeneration remains unknown. To address this, we generated a novel mouse model in which androgen receptor (AR) is ablated from ~75% of adult Leydig stem cell/cell progenitors, from fetal life onward (Leydig cell AR knockout mice), permitting interrogation of the specific roles of autocrine Leydig cell AR signaling through comparison to adjacent AR‐retaining Leydig cells, testes from littermate controls, and to human testes, including from patients with complete androgen insensitivity syndrome (CAIS). This revealed that autocrine AR signaling is dispensable for the attainment of final Leydig cell number but is essential for Leydig cell maturation and regulation of steroidogenic enzymes in adulthood. Furthermore, these studies reveal that autocrine AR signaling in Leydig cells protects against late‐onset degeneration of the seminiferous epithelium in mice and inhibits Leydig cell apoptosis in both adult mice and patients with CAIS, possibly via opposing aberrant estrogen signaling. We conclude that autocrine androgen action within Leydig cells is essential for the lifelong support of spermatogenesis and the development and lifelong health of Leydig cells.—O'Hara, L., McInnes, K., Simitsidellis, I., Morgan, S., Atanassova, N., Slowikowska‐Hilczer, J., Kula, K., Szarras‐Czapnik, M., Milne, L., Mitchell, R. T., Smith, L. B., Autocrine androgen action is essential for Leydig cell maturation and function, and protects against late‐onset Leydig cell apoptosis in both mice andmen. FASEB J. 29, 894–910 (2015). www.fasebj.org