共 48 条
SH2-B is required for both male and female reproduction
被引:55
作者:
Ohtsuka, S
Takaki, S
Iseki, M
Miyoshi, K
Nakagata, N
Kataoka, Y
Yoshida, N
Takatsu, K
Yoshimura, A
机构:
[1] Kyushu Univ, Med Inst Bioregulat, Div Mol & Cellular Immunol, Higashi Ku, Fukuoka 8128582, Japan
[2] Kurume Univ, Inst Life Sci, Div Mol Genet, Kurume, Fukuoka 8390861, Japan
[3] Kumamoto Univ, Ctr Anim Res & Dev, Div Reprod Engn, Kumamoto 8600811, Japan
[4] Univ Tokyo, Inst Med Sci, Div Immunol, Dept Microbiol & Immunol,Minato Ku, Tokyo 1088639, Japan
[5] Univ Tokyo, Inst Med Sci, Lab Gene Express & Regulat, Ctr Med Expt,Minato Ku, Tokyo 1088639, Japan
关键词:
D O I:
10.1128/MCB.22.9.3066-3077.2002
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:
Many growth factors and hormones modulate the reproductive status in mammals. Among these, insulin and insulin-like growth factor I (IGF-I) regulate the development of gonadal tissues. SH2-B has been shown to interact with insulin and IGF-I receptors, although the role of SH2-B in these signals has not been clarified. To investigate the role of SH2-B, we generated mice with a targeted disruption of the SH2-B gene. Both male and female SH2-B-/- mice showed slight retardation in growth and impaired fertility. Female knockout mice possess small, anovulatory ovaries with reduced numbers of follicles and male SH2-B-/- mice have small testes with a reduced number of sperm. SH2-B-/- cumulus cells do not respond to either follicle-stimulating hormone or IGF-I. These data suggest that SH2-B plays a critical role in the IGF-1-mediated reproductive pathway in mice.
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页码:3066 / 3077
页数:12
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