Human Molecular Genetics Advance Access published online on September 19, 2006
Human Molecular Genetics, doi:10.1093/hmg/ddl393
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1 Departamento de Bioquímica y Biología Molecular y Celular, Facultad de Veterinaria, Universidad de Zaragoza
* To whom correspondence should be addressed. In human reproduction, hyperhomocysteinaemia has been reported as a risk factor for early pregnancy loss and congenital birth defects. Hyperhomocysteinaemia is also recognized as a cause of maternal obstetric complications such as preeclampsia. The role of plasma hyperhomocysteinemia in female fertility was examined using cystathionine beta synthase knockout (cbs KO) mice. Cbs KO females were infertile, showed alterations in the estrus cycle, and an increased progesterone response during pseudopregnancy induction. Both cbs KO ovaries and ovulated oocytes showed no major morphological alterations. However, placental and uterine masses were decreased at day 18 of pregnancy and showed morphological abnormalities. In cbs-KO pregnant females the number of uterine implantation sites was not decreased despite the low number of surviving embryos. Fertility was restored when cbs deficient ovaries were transplanted to normal ovarectomized recipients. We detected an increased uterine expression of Grp78, a marker of endoplasmic reticulum stress, that was accompanied by decreased levels of uterine cbs mRNA in both hyperhomocysteinemic heterozygous (fertile) and homozygous (non fertile) females. Our results indicate that cbs -/- female infertility is a consequence of uterine failure and demonstrate that uterine endoplasmic reticulum stress and cbs expression are not determinant of infertility suggesting that uterine dysfunction is a consequence of either hyperhomocysteinemia, or other factor(s) in the uterine environment of cbs -/- animals. In summary, these studies demonstrate the potential importance of homocysteine levels for uterine handling of embryos.
Received July 13, 2006
Accepted September 11, 2006
Article
Cystathionine
Mario A. Guzmán 1, María A. Navarro 1, Ricardo Carnicer 1, Alfonso J. Sarría 1, Sergio Acín 1, Carmen Arnal 2, Pedro Muniesa 3, Joaquín C. Surra 1, José M. Arbonés-Mainar 1, Nobuyo Maeda 4, and Jesús Osada 5 *
-synthase is essential for female reproductive function
2 Departamento de Patología Animal, Facultad de Veterinaria, Universidad de Zaragoza
3 Departamento de Anatomía y Embriología, Facultad de Veterinaria, Universidad de Zaragoza
4 Department of Pathology, University of North Carolina at Chapel Hill, USA
5 Department of Biochemistry and Molecular Biology, Facultad de Veterinaria, Universidad de Zaragoza, Miguel Servet, 177, E-50013 Zaragoza, Spain
Jesús Osada, E-mail: Josada{at}unizar.es
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