The Bile Acid Synthesis Pathway Is Present and Functional in the Human Ovary

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The Bile Acid Synthesis Pathway Is Present and Functional in the Human Ovary

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Title: The Bile Acid Synthesis Pathway Is Present and Functional in the Human Ovary
Author: Nierstenhoefer, Maik; Tobiasch, Edda; Usheva, Anny; Smith, Laura; Yoo, Sang Wook; Penzias, Alan Stewart

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Citation: Smith, Laura P., Maik Nierstenhoefer, Sang Wook Yoo, Alan S. Penzias, Edda Tobiasch, and Anny Usheva. 2009. The Bile Acid Synthesis Pathway Is Present and Functional in the Human Ovary. PLoS ONE 4(10): e7333.
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Abstract: Background: Bile acids, end products of the pathway for cholesterol elimination, are required for dietary lipid and fat-soluble vitamin absorption and maintain the balance between cholesterol synthesis in the liver and cholesterol excretion. They are composed of a steroid structure and are primarily made in the liver by the oxidation of cholesterol. Cholesterol is also highly abundant in the human ovarian follicle, where it is used in the formation of the sex steroids. Methodology/Principal Findings: Here we describe for the first time evidence that all aspects of the bile acid synthesis pathway are present in the human ovarian follicle, including the enzymes in both the classical and alternative pathways, the nuclear receptors known to regulate the pathway, and the end product bile acids. Furthermore, we provide functional evidence that bile acids are produced by the human follicular granulosa cells in response to cholesterol presence in the culture media. Conclusions/Significance: These findings establish a novel pathway present in the human ovarian follicle that has the capacity to compete directly with sex steroid synthesis.
Published Version: doi:10.1371/journal.pone.0007333
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752198/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:4742698

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