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Liver X receptors and fat cell metabolism

Liver X receptors (LXRs) are members of the nuclear receptor family and are present in two isoforms, α and β, encoded by two separate genes. Originally described in the liver, LXRs have in the last 15 years been implicated in central metabolic pathways, including bile acid synthesis, lipid and gluco...

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Detalles Bibliográficos
Autores principales: Laurencikiene, J, Rydén, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520012/
https://www.ncbi.nlm.nih.gov/pubmed/22370853
http://dx.doi.org/10.1038/ijo.2012.21
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author Laurencikiene, J
Rydén, M
author_facet Laurencikiene, J
Rydén, M
author_sort Laurencikiene, J
collection PubMed
description Liver X receptors (LXRs) are members of the nuclear receptor family and are present in two isoforms, α and β, encoded by two separate genes. Originally described in the liver, LXRs have in the last 15 years been implicated in central metabolic pathways, including bile acid synthesis, lipid and glucose homeostasis. Although the vast majority of studies have been performed in non-adipose cells/tissues, results in recent years suggest that LXRs may have important modulatory roles in adipose tissue and adipocytes. Although several authors have published reviews on LXR, there have been no attempts to summarize the effects reported specifically in adipose systems. This overview gives a brief introduction to LXR and describes the sometimes-contradictory results obtained in murine cell systems and in rodent adipose tissue. The so far very limited number of studies performed in human adipocytes and adipose tissue are also presented. It should be apparent that although LXR may impact on several different pathways in metabolism, the clinical role of LXR modulation in adipose tissue is still not clear.
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spelling pubmed-35200122012-12-12 Liver X receptors and fat cell metabolism Laurencikiene, J Rydén, M Int J Obes (Lond) Review Liver X receptors (LXRs) are members of the nuclear receptor family and are present in two isoforms, α and β, encoded by two separate genes. Originally described in the liver, LXRs have in the last 15 years been implicated in central metabolic pathways, including bile acid synthesis, lipid and glucose homeostasis. Although the vast majority of studies have been performed in non-adipose cells/tissues, results in recent years suggest that LXRs may have important modulatory roles in adipose tissue and adipocytes. Although several authors have published reviews on LXR, there have been no attempts to summarize the effects reported specifically in adipose systems. This overview gives a brief introduction to LXR and describes the sometimes-contradictory results obtained in murine cell systems and in rodent adipose tissue. The so far very limited number of studies performed in human adipocytes and adipose tissue are also presented. It should be apparent that although LXR may impact on several different pathways in metabolism, the clinical role of LXR modulation in adipose tissue is still not clear. Nature Publishing Group 2012-12 2012-02-28 /pmc/articles/PMC3520012/ /pubmed/22370853 http://dx.doi.org/10.1038/ijo.2012.21 Text en Copyright © 2012 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Review
Laurencikiene, J
Rydén, M
Liver X receptors and fat cell metabolism
title Liver X receptors and fat cell metabolism
title_full Liver X receptors and fat cell metabolism
title_fullStr Liver X receptors and fat cell metabolism
title_full_unstemmed Liver X receptors and fat cell metabolism
title_short Liver X receptors and fat cell metabolism
title_sort liver x receptors and fat cell metabolism
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520012/
https://www.ncbi.nlm.nih.gov/pubmed/22370853
http://dx.doi.org/10.1038/ijo.2012.21
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