PPARs Integrate the Mammalian Clock and Energy Metabolism

Peroxisome proliferator-activated receptors (PPARs) are a group of nuclear receptors that function as transcription factors regulating the expression of numerous target genes. PPARs play an essential role in various physiological and pathological processes, especially in energy metabolism. It has lo...

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Main Authors: Lihong Chen, Guangrui Yang
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:PPAR Research
Online Access:http://dx.doi.org/10.1155/2014/653017
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author Lihong Chen
Guangrui Yang
author_facet Lihong Chen
Guangrui Yang
author_sort Lihong Chen
collection DOAJ
description Peroxisome proliferator-activated receptors (PPARs) are a group of nuclear receptors that function as transcription factors regulating the expression of numerous target genes. PPARs play an essential role in various physiological and pathological processes, especially in energy metabolism. It has long been known that metabolism and circadian clocks are tightly intertwined. However, the mechanism of how they influence each other is not fully understood. Recently, all three PPAR isoforms were found to be rhythmically expressed in given mouse tissues. Among them, PPARα and PPARγ are direct regulators of core clock components, Bmal1 and Rev-erbα, and, conversely, PPARα is also a direct Bmal1 target gene. More importantly, recent studies using knockout mice revealed that all PPARs exert given functions in a circadian manner. These findings demonstrated a novel role of PPARs as regulators in correlating circadian rhythm and metabolism. In this review, we summarize advances in our understanding of PPARs in circadian regulation.
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spelling doaj-art-5909ab6ba685406d803431775c0976b52025-02-03T06:04:47ZengWileyPPAR Research1687-47571687-47652014-01-01201410.1155/2014/653017653017PPARs Integrate the Mammalian Clock and Energy MetabolismLihong Chen0Guangrui Yang1The Institute for Translational Medicine and Therapeutics, Translational Research Center, University of Pennsylvania, 3400 Civic Center Boulevard, Building 421, Philadelphia, PA 19104-5158, USAThe Institute for Translational Medicine and Therapeutics, Translational Research Center, University of Pennsylvania, 3400 Civic Center Boulevard, Building 421, Philadelphia, PA 19104-5158, USAPeroxisome proliferator-activated receptors (PPARs) are a group of nuclear receptors that function as transcription factors regulating the expression of numerous target genes. PPARs play an essential role in various physiological and pathological processes, especially in energy metabolism. It has long been known that metabolism and circadian clocks are tightly intertwined. However, the mechanism of how they influence each other is not fully understood. Recently, all three PPAR isoforms were found to be rhythmically expressed in given mouse tissues. Among them, PPARα and PPARγ are direct regulators of core clock components, Bmal1 and Rev-erbα, and, conversely, PPARα is also a direct Bmal1 target gene. More importantly, recent studies using knockout mice revealed that all PPARs exert given functions in a circadian manner. These findings demonstrated a novel role of PPARs as regulators in correlating circadian rhythm and metabolism. In this review, we summarize advances in our understanding of PPARs in circadian regulation.http://dx.doi.org/10.1155/2014/653017
spellingShingle Lihong Chen
Guangrui Yang
PPARs Integrate the Mammalian Clock and Energy Metabolism
PPAR Research
title PPARs Integrate the Mammalian Clock and Energy Metabolism
title_full PPARs Integrate the Mammalian Clock and Energy Metabolism
title_fullStr PPARs Integrate the Mammalian Clock and Energy Metabolism
title_full_unstemmed PPARs Integrate the Mammalian Clock and Energy Metabolism
title_short PPARs Integrate the Mammalian Clock and Energy Metabolism
title_sort ppars integrate the mammalian clock and energy metabolism
url http://dx.doi.org/10.1155/2014/653017
work_keys_str_mv AT lihongchen pparsintegratethemammalianclockandenergymetabolism
AT guangruiyang pparsintegratethemammalianclockandenergymetabolism