Time-resolved expression profiling of the nuclear receptor superfamily in human adipogenesis.

BACKGROUND: The differentiation of fibroblast-like pre-adipocytes to lipid-loaded adipocytes is regulated by a network of transcription factors, the most prominent one being the nuclear receptor peroxisome proliferator-activated receptor (PPAR) γ. However, many of the other 47 members of the nuclear...

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Main Authors: Mari Lahnalampi, Merja Heinäniemi, Lasse Sinkkonen, Martin Wabitsch, Carsten Carlberg
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2946337?pdf=render
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author Mari Lahnalampi
Merja Heinäniemi
Lasse Sinkkonen
Martin Wabitsch
Carsten Carlberg
author_facet Mari Lahnalampi
Merja Heinäniemi
Lasse Sinkkonen
Martin Wabitsch
Carsten Carlberg
author_sort Mari Lahnalampi
collection DOAJ
description BACKGROUND: The differentiation of fibroblast-like pre-adipocytes to lipid-loaded adipocytes is regulated by a network of transcription factors, the most prominent one being the nuclear receptor peroxisome proliferator-activated receptor (PPAR) γ. However, many of the other 47 members of the nuclear receptor superfamily have an impact on adipogenesis, which in human cells has not been investigated in detail. METHODOLOGY/PRINCIPAL FINDINGS: We analyzed by quantitative PCR all human nuclear receptors at multiple time points during differentiation of SGBS pre-adipocytes. The earliest effect was the down-regulation of the genes RARG, PPARD, REV-ERBA, REV-ERBB, VDR and GR followed by the up-regulation of PPARG, LXRA and AR. These observations are supported with data from 3T3-L1 mouse pre-adipocytes and primary human adipocytes. Investigation of the effects of the individual differentiation mix components in short-term treatments and of their omission from the full mix showed that the expression levels of the early-regulated nuclear receptor genes were most affected by the glucocorticoid receptor (GR) ligand cortisol and the phosphodiesterase inhibitor IBMX. Interestingly, the effects of both compounds converged to repress the genes PPARD, REV-ERBA, REV-ERBB, VDR and GR, whereas cortisol and IBMX showed antagonistic interaction for PPARG, LXRA and AR causing a time lag in their up-regulation. We hypothesize that the well-known auto-repression of GR fine-tunes the detected early responses. Consistently, chromatin immunoprecipitation experiments showed that GR association increased on the transcription start sites of the genes RARG, REV-ERBB, VDR and GR. CONCLUSIONS/SIGNIFICANCE: Adipocyte differentiation is a process, in which many members of the nuclear receptor superfamily change their mRNA expression. The actions of cortisol and IBMX converged to repress several nuclear receptors early in differentiation, while up-regulation of other nuclear receptor genes showed a time lag due to antagonisms of the signals. Our results place GR and its ligand cortisol as central regulatory factors controlling early regulatory events in human adipogenesis that precedes the regulation of the later events by PPARG.
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spelling doaj.art-d8472418811b4bd39c53d55e6d9ace7b2022-12-22T00:52:13ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-01-0159e1299110.1371/journal.pone.0012991Time-resolved expression profiling of the nuclear receptor superfamily in human adipogenesis.Mari LahnalampiMerja HeinäniemiLasse SinkkonenMartin WabitschCarsten CarlbergBACKGROUND: The differentiation of fibroblast-like pre-adipocytes to lipid-loaded adipocytes is regulated by a network of transcription factors, the most prominent one being the nuclear receptor peroxisome proliferator-activated receptor (PPAR) γ. However, many of the other 47 members of the nuclear receptor superfamily have an impact on adipogenesis, which in human cells has not been investigated in detail. METHODOLOGY/PRINCIPAL FINDINGS: We analyzed by quantitative PCR all human nuclear receptors at multiple time points during differentiation of SGBS pre-adipocytes. The earliest effect was the down-regulation of the genes RARG, PPARD, REV-ERBA, REV-ERBB, VDR and GR followed by the up-regulation of PPARG, LXRA and AR. These observations are supported with data from 3T3-L1 mouse pre-adipocytes and primary human adipocytes. Investigation of the effects of the individual differentiation mix components in short-term treatments and of their omission from the full mix showed that the expression levels of the early-regulated nuclear receptor genes were most affected by the glucocorticoid receptor (GR) ligand cortisol and the phosphodiesterase inhibitor IBMX. Interestingly, the effects of both compounds converged to repress the genes PPARD, REV-ERBA, REV-ERBB, VDR and GR, whereas cortisol and IBMX showed antagonistic interaction for PPARG, LXRA and AR causing a time lag in their up-regulation. We hypothesize that the well-known auto-repression of GR fine-tunes the detected early responses. Consistently, chromatin immunoprecipitation experiments showed that GR association increased on the transcription start sites of the genes RARG, REV-ERBB, VDR and GR. CONCLUSIONS/SIGNIFICANCE: Adipocyte differentiation is a process, in which many members of the nuclear receptor superfamily change their mRNA expression. The actions of cortisol and IBMX converged to repress several nuclear receptors early in differentiation, while up-regulation of other nuclear receptor genes showed a time lag due to antagonisms of the signals. Our results place GR and its ligand cortisol as central regulatory factors controlling early regulatory events in human adipogenesis that precedes the regulation of the later events by PPARG.http://europepmc.org/articles/PMC2946337?pdf=render
spellingShingle Mari Lahnalampi
Merja Heinäniemi
Lasse Sinkkonen
Martin Wabitsch
Carsten Carlberg
Time-resolved expression profiling of the nuclear receptor superfamily in human adipogenesis.
PLoS ONE
title Time-resolved expression profiling of the nuclear receptor superfamily in human adipogenesis.
title_full Time-resolved expression profiling of the nuclear receptor superfamily in human adipogenesis.
title_fullStr Time-resolved expression profiling of the nuclear receptor superfamily in human adipogenesis.
title_full_unstemmed Time-resolved expression profiling of the nuclear receptor superfamily in human adipogenesis.
title_short Time-resolved expression profiling of the nuclear receptor superfamily in human adipogenesis.
title_sort time resolved expression profiling of the nuclear receptor superfamily in human adipogenesis
url http://europepmc.org/articles/PMC2946337?pdf=render
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