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c‐Flip expression and function in fetal mouse gonocytes
Author(s) -
Giampietri Claudia,
Petrungaro Simonetta,
Klinger Francesca G.,
Coluccia Pierpaolo,
Paone Alessio,
Vivarelli Elisabetta,
Filippini Antonio,
De Cesaris Paola,
De Felici Massimo,
Ziparo Elio
Publication year - 2006
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.05-4626fje
Subject(s) - gonocyte , apoptosis , biology , fetus , endocrinology , medicine , microbiology and biotechnology , germ cell , programmed cell death , spermatogenesis , sertoli cell , genetics , gene , pregnancy
Apoptosis is a key mechanism in spermatogenesis, and in testis, most gonocytes degenerate at fetal and postnatal ages to select a cell subset committed to become germ stem cells. The aim of the present study is to investigate mechanisms controlling the massive apoptosis of fetal gonocytes. We evaluated the expression and function of c‐Flip, an apoptosis inhibitor known to interfere with the proapoptotic Fas‐signaling pathway in a variety of cell types, but never investigated in fetal testis. Expression of c‐Flip long isoform (c‐FlipL) within fetal testis was localized in gonocytes at 16.5 and 18.5 days post coitum (dpc), both at the mRNA and protein level, while it was weakly expressed or undetectable at earlier stages. Moreover, Fas protein was found in fetal testes at 13.5, 16.5, and 18.5 dpc. Testes at 18.5 dpc, expressing high levels of c‐FlipL, were resistant to Fas‐induced apoptosis while they became highly sensitive when c‐FlipL was inhibited by antisense c‐Flip oligos. In addition, there was an inverse relation between gonocyte spontaneous apoptosis sensitivity and c‐FlipL levels. Furthermore, caspase‐10 activity was inversely related with c‐FlipL expression, suggesting that caspase‐10 might be a target of c‐FlipL. These data represent the first evidence demonstrating c‐Flip expression in fetal testes and its role in protecting gonocytes from Fas‐dependent apoptosis.