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Cholesterol metabolism pathways – are the intermediates more important than the products?

Every cell in vertebrates possesses the machinery to synthesise cholesterol and to metabolise it. The major route of cholesterol metabolism is conversion to bile acids. Bile acids themselves are interesting molecules being ligands to nuclear and G protein‐coupled receptors, but perhaps the intermedi...

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Detalles Bibliográficos
Autores principales: Wang, Yuqin, Yutuc, Eylan, Griffiths, William J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8653896/
https://www.ncbi.nlm.nih.gov/pubmed/33506652
http://dx.doi.org/10.1111/febs.15727
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author Wang, Yuqin
Yutuc, Eylan
Griffiths, William J.
author_facet Wang, Yuqin
Yutuc, Eylan
Griffiths, William J.
author_sort Wang, Yuqin
collection PubMed
description Every cell in vertebrates possesses the machinery to synthesise cholesterol and to metabolise it. The major route of cholesterol metabolism is conversion to bile acids. Bile acids themselves are interesting molecules being ligands to nuclear and G protein‐coupled receptors, but perhaps the intermediates in the bile acid biosynthesis pathways are even more interesting and equally important. Here, we discuss the biological activity of the different intermediates generated in the various bile acid biosynthesis pathways. We put forward the hypothesis that the acidic pathway of bile acid biosynthesis has primary evolved to generate signalling molecules and its utilisation by hepatocytes provides an added bonus of producing bile acids to aid absorption of lipids in the intestine.
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spelling pubmed-86538962021-12-20 Cholesterol metabolism pathways – are the intermediates more important than the products? Wang, Yuqin Yutuc, Eylan Griffiths, William J. FEBS J State‐of‐the‐Art Reviews Every cell in vertebrates possesses the machinery to synthesise cholesterol and to metabolise it. The major route of cholesterol metabolism is conversion to bile acids. Bile acids themselves are interesting molecules being ligands to nuclear and G protein‐coupled receptors, but perhaps the intermediates in the bile acid biosynthesis pathways are even more interesting and equally important. Here, we discuss the biological activity of the different intermediates generated in the various bile acid biosynthesis pathways. We put forward the hypothesis that the acidic pathway of bile acid biosynthesis has primary evolved to generate signalling molecules and its utilisation by hepatocytes provides an added bonus of producing bile acids to aid absorption of lipids in the intestine. John Wiley and Sons Inc. 2021-02-17 2021-06 /pmc/articles/PMC8653896/ /pubmed/33506652 http://dx.doi.org/10.1111/febs.15727 Text en © 2021 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle State‐of‐the‐Art Reviews
Wang, Yuqin
Yutuc, Eylan
Griffiths, William J.
Cholesterol metabolism pathways – are the intermediates more important than the products?
title Cholesterol metabolism pathways – are the intermediates more important than the products?
title_full Cholesterol metabolism pathways – are the intermediates more important than the products?
title_fullStr Cholesterol metabolism pathways – are the intermediates more important than the products?
title_full_unstemmed Cholesterol metabolism pathways – are the intermediates more important than the products?
title_short Cholesterol metabolism pathways – are the intermediates more important than the products?
title_sort cholesterol metabolism pathways – are the intermediates more important than the products?
topic State‐of‐the‐Art Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8653896/
https://www.ncbi.nlm.nih.gov/pubmed/33506652
http://dx.doi.org/10.1111/febs.15727
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