Fas expression correlates with human germ cell degeneration in meiotic and post-meiotic arrest of spermatogenesis

• Published in: Molecular human reproduction Vol. 8; no. 3; pp. 213 - 220
• Main Authors: Francavilla, Sandro, D'Abrizio, Piera, Cordeschi, Giuliana, Pelliccione, Fiore, Necozione, Stefano, Ulisse, Salvatore, Properzi, Giuliana, Francavilla, Felice
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01.03.2002; Oxford Publishing Limited (England)
• Subjects: Ageing, cell death; apoptosis; Biological and medical sciences; Cell physiology; Fas; fas Receptor - biosynthesis; Fundamental and applied biological sciences. Psychology; Humans; immunohistochemistry; Immunohistochemistry - methods; Infertility, Male; Male; Meiosis - physiology; Molecular and cellular biology; spermatogenesis; Spermatogenesis - physiology; Spermatozoa - cytology; Spermatozoa - metabolism; Testis - cytology; Testis - metabolism; ultrastructure; Human; Ripening; Fas ligand; Spermatocyte; Spermatogenesis; Meiosis; Germinal cell; Gene expression; Spermatid; Apoptosis
• ISSN: 1360-9947; 1460-2407; 1460-2407
• DOI: 10.1093/molehr/8.3.213

Degeneration of human male germ cells was analysed by means of light (LM) and transmission electron (TEM) microscopy. The frequency of degenerating cells was correlated with that of Fas-expressing germ cells in human testes with normal spermatogenesis (n = 10), complete early maturation arrest (EMA) (n = 10) or incomplete late maturation arrest (LMA; n = 10) of spermatogenesis. LM analysis of testis sections with normal spermatogenesis indicated that degenerating germ cells were localized in the adluminal compartment of the seminiferous epithelium. TEM showed that apoptotic cells were mostly primary spermatocytes and, to a lesser extent, round or early elongating spermatids. Apoptotic germ cells appeared to be eliminated either in the seminiferous lumen or by Sertoli cell phagocytosis. An increased number of degenerating cells was observed in testes with LMA as compared with normal testes and testes with EMA of spermatogenesis (P < 0.001, Wilcoxon's rank sum test). Comparison of these results with those obtained from immunohistochemistry experiments demonstrated a tight correlation between the number of apoptotic cells and the number of Fas-expressing germ cells (P = 0.001, Spearman's rank = 0.69). These findings suggest that altered meiotic and post-meiotic germ cell maturation might be associated with an up-regulation of Fas gene expression capable of triggering apoptotic elimination of defective germ cells.