C-FlipL is expressed in undifferentiated mouse male germ cells

被引:10
作者
Giampietri, Claudia [1 ]
Petrungaro, Simonetta
Coluccia, Plerpaolo
Antonangeli, Fabrizio
Paone, Alessio
Padula, Fabrizio
De Cesaris, Paola
Ziparo, Elio
Filippini, Antonio
机构
[1] Univ Roma La Sapienza, Ist Pasteur, Fdn Cenci Bolognetti, Dept Histol & Med Embryol, I-00161 Rome, Italy
[2] Univ Roma La Sapienza, Dept Surg P Valdoni, I-00161 Rome, Italy
[3] Univ Aquila, Dept Expt Med, I-67100 Laquila, Italy
关键词
testis; apoptosis; stem cells; caspases;
D O I
10.1016/j.febslet.2006.10.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apoptosis represents a fundamental process during fetal/post-natal testis development. Therefore pro- and antiapoptotic proteins are essential to regulate testis physiology. c-FliP(L) is a known inhibitor of caspase 8110 activity; in this study its perinatal expression in mouse male germ cells was investigated. In testis sections and seminiferous tubule whole mount c-FliPL was found to be expressed in undifferentiated spermatogonia and to co-localize with germ stem cells markers. In vivo investigations in the vitamin-A deficient mouse, lacking differentiated germ cells, confirmed c-FliP(L) expression in undifferentiated spermatogonia. Further analyses showed Fas expression but no significant caspase 8/10 activity when c-FliP(L) was highly expressed. Altogether these data suggest that c-Flip may control the survival rate of undifferentiated spermatogonia. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:6109 / 6114
页数:6
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