SH2-B Is Required for Both Male and Female Reproduction

Author:

Ohtsuka Satoshi1,Takaki Satoshi2,Iseki Masanori2,Miyoshi Kanta3,Nakagata Naomi4,Kataoka Yuki5,Yoshida Nobuaki5,Takatsu Kiyoshi2,Yoshimura Akihiko13

Affiliation:

1. Division of Molecular Genetics, Institute of Life Science, Kurume University, Kurume 839-0861

2. Division of Immunology, Department of Microbiology and Immunology

3. Division of Molecular and Cellular Immunology, Medical Institute of Bioregulation, Kyushu University, Higashi-ku, Fukuoka 812-8582

4. Division of Reproductive Engineering, Center for Animal Resources & Development, Kumamoto University, Kumamoto 860-0811, Japan

5. Laboratory of Gene Expression and Regulation, Center for Experimental Medicine, Institute of Medical Science, The University of Tokyo, Minato-ku 108-8639

Abstract

ABSTRACT 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-I-mediated reproductive pathway in mice.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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