A mouse Sertoli cell line expressing anti-Mullerian hormone and its type II receptor

被引:53
作者
Dutertre, M
Rey, R
Porteu, A
Josso, N
Picard, JY
机构
[1] Ecole Normale Super, Dept Biol, Unite Rech Endocrinol Dev, INSERM, F-92120 Montrouge, France
[2] Inst Cochin Genet Mol, INSERM, Unite Rech Physiol & Pathol Genet & Mol, F-75014 Paris, France
关键词
anti-Mullerian hormone; Mullerian inhibiting substance; anti-Mullerian hormone receptor; Sertoli cell line; testis tumour; targeted oncogenesis;
D O I
10.1016/S0303-7207(97)00214-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Anti-Mullerian hormone (AMH) induces the regression of Mullerian ducts in the male foetus; it is secreted by prepubertal testicular Sertoli cells and repressed at puberty. Using an AMH promoter/Simian virus 40 (SV40) oncogene fusion gene, we generated transgenic mouse lines exhibiting heritable Sertoli cell tumorigenesis. One cell line, derived from an adult male, expressed mRNAs characteristic of mature Sertoli cells, but no AMH. Two other cell lines were obtained from pretumoral testes at 6.5 days. One was cloned to yield SMAT1, whose expression pattern was characteristic of prepubertal Sertoli cells, namely no transferrin and high SF-1 and AMH expression. SMAT1 also secretes AMH protein into the culture medium and expresses the AMH receptor. To the best of our knowledge, this is the first Sertoli cell line stably expressing AMH and its receptor. Our results show that, in targeted oncogenesis, the timing of cell line derivation plays a critical role even when using a developmentally regulated promoter. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:57 / 65
页数:9
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