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
相关论文
共 27 条
[11]   Inhibition of death receptor signals by cellular FLIP [J].
Irmler, M ;
Thome, M ;
Hahne, M ;
Schneider, P ;
Hofmann, B ;
Steiner, V ;
Bodmer, JL ;
Schroter, M ;
Burns, K ;
Mattmann, C ;
Rimoldi, D ;
French, LE ;
Tschopp, J .
NATURE, 1997, 388 (6638) :190-195
[12]   Human CD34+ hematopoietic stem/progenitor cells express high levels of FLIP and are resistant to Fas-mediated apoptosis [J].
Kim, H ;
Whartenby, KA ;
Georgantas, RW ;
Wingard, J ;
Civin, CI .
STEM CELLS, 2002, 20 (02) :174-182
[13]  
KOUBOVA J, 2006, P NATL ACAD SCI US
[14]   SPERMATOCYTE TOXICITY OF 2-METHOXYETHANOL (ME) IN RATS AND GUINEA-PIGS - EVIDENCE FOR THE INDUCTION OF APOPTOSIS [J].
KU, WW ;
WINE, RN ;
CHAE, BY ;
GHANAYEM, BI ;
CHAPIN, RE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1995, 134 (01) :100-110
[15]   Culture conditions and single growth factors affect fate determination of mouse spermatogonial stem cells [J].
Kubota, H ;
Avarbock, MR ;
Brinster, RL .
BIOLOGY OF REPRODUCTION, 2004, 71 (03) :722-731
[16]   The Fas system is a key regulator of germ cell apoptosis in the testis [J].
Lee, JW ;
Richburg, JH ;
Younkin, SC ;
Boekelheide, K .
ENDOCRINOLOGY, 1997, 138 (05) :2081-2088
[17]   MORPHOLOGY, PROLIFERATION, AND DIFFERENTIATION OF UNDIFFERENTIATED SPERMATOGONIA IN THE CHINESE-HAMSTER AND THE RAM [J].
LOK, D ;
WEENK, D ;
DEROOIJ, DG .
ANATOMICAL RECORD, 1982, 203 (01) :83-99
[18]   THE FAS DEATH FACTOR [J].
NAGATA, S ;
GOLSTEIN, P .
SCIENCE, 1995, 267 (5203) :1449-1456
[19]   Developmental expression of BMP4/ALK3/SMAD5 signaling pathway in the mouse testis: a potential role of BMP4 in spermatogonia differentiation [J].
Pellegrini, M ;
Grimaldi, P ;
Rossi, P ;
Geremia, R ;
Dolci, S .
JOURNAL OF CELL SCIENCE, 2003, 116 (16) :3363-3372
[20]   FLICE-inhibitory protein expression during macrophage differentiation confers resistance to Fas-mediated apoptosis [J].
Perlman, H ;
Pagliari, LJ ;
Georganas, C ;
Mano, T ;
Walsh, K ;
Pope, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (11) :1679-1688