Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/23139
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Type: Journal article
Title: Null mutation in transforming growth factor β1 disrupts ovarian function and causes oocyte incompetence and early embryo arrest
Other Titles: Null mutation in transforming growth factor beta1 disrupts ovarian function and causes oocyte incompetence and early embryo arrest
Author: Ingman, W.
Robker, R.
Woittiez, K.
Robertson, S.
Citation: Endocrinology, 2006; 147(2):835-845
Publisher: Endocrine Soc
Issue Date: 2006
ISSN: 0013-7227
0013-7227
Statement of
Responsibility: 
Wendy V. Ingman, Rebecca L. Robker, Karen Woittiez, and Sarah A. Robertson
Abstract: TGFbeta1 is implicated in regulation of ovarian function and the events of early pregnancy. We have investigated the effect of null mutation in the Tgfbeta1 gene on reproductive function in female mice. The reproductive capacity of TGFbeta1 null mutant females was severely impaired, leading to almost complete infertility. Onset of sexual maturity was delayed, after which ovarian function was disrupted, with extended ovarian cycles, irregular ovulation, and a 40% reduction in oocytes ovulated. Serum FSH and estrogen content were normal, but TGFbeta1 null mutant mice failed to display the characteristic proestrus surge in circulating LH. Ovarian hyperstimulation with exogenous gonadotropins elicited normal ovulation rates in TGFbeta1 null mutant mice. After mating with wild-type stud males, serum progesterone content was reduced by 75% associated with altered ovarian expression of mRNAs encoding steroidogenic enzymes 3beta-hydroxysteroid dehydrogenase-1 and P450 17 alpha-hydroxylase/C17-20-lyase. Embryos recovered from TGFbeta1 null mutant females were developmentally arrested in the morula stage and rarely progressed to blastocysts. Attempts to rescue embryos by exogenous progesterone administration and in vitro culture were unsuccessful, and in vitro fertilization and culture experiments demonstrated that impaired development is unlikely to result from lack of maternal tract TGFbeta1. We conclude that embryo arrest is due to developmental incompetence in oocytes developed in a TGFbeta1-deficient follicular environment. This study demonstrates that TGFbeta1 is a critical determinant of normal ovarian function, operating through regulation of LH activity and generation of oocytes competent for embryonic development and successful initiation of pregnancy.
Keywords: Ovary; Ovum; Animals; Mice, Knockout; Mice; Mice, SCID; Infertility, Female; Progesterone; Transforming Growth Factor beta; Embryonic Development; Estrous Cycle; Ovulation; Pregnancy; Pregnancy, Animal; Sexual Maturation; Mutation; Female; Transforming Growth Factor beta1
Description: Copyright © 2006 by The Endocrine Society
RMID: 0020060215
DOI: 10.1210/en.2005-1189
Appears in Collections:Obstetrics and Gynaecology publications

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