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Altered Transcription Factor Expression Responses to Exercise in Insulin Resistance

PURPOSE: Insulin resistant muscle is resistant to gene expression changes induced by acute exercise. This study was undertaken to identify transcription factors that differentially respond to exercise in insulin resistance. Candidate transcription factors were identified from analysis of 5′-untransl...

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Autores principales: Zapata-Bustos, Rocio, Finlayson, Jean, Langlais, Paul R., Coletta, Dawn K., Luo, Moulun, Grandjean, Danielle, De Filippis, Elena A., Mandarino, Lawrence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8058368/
https://www.ncbi.nlm.nih.gov/pubmed/33897458
http://dx.doi.org/10.3389/fphys.2021.649461
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author Zapata-Bustos, Rocio
Finlayson, Jean
Langlais, Paul R.
Coletta, Dawn K.
Luo, Moulun
Grandjean, Danielle
De Filippis, Elena A.
Mandarino, Lawrence
author_facet Zapata-Bustos, Rocio
Finlayson, Jean
Langlais, Paul R.
Coletta, Dawn K.
Luo, Moulun
Grandjean, Danielle
De Filippis, Elena A.
Mandarino, Lawrence
author_sort Zapata-Bustos, Rocio
collection PubMed
description PURPOSE: Insulin resistant muscle is resistant to gene expression changes induced by acute exercise. This study was undertaken to identify transcription factors that differentially respond to exercise in insulin resistance. Candidate transcription factors were identified from analysis of 5′-untranslated regions (5′-UTRs) of exercise responsive genes and from analysis of the 5′-UTRs of genes coding for proteins that differ in abundance in insulin resistance. RESEARCH DESIGN AND METHODS: Twenty participants took part in this study. Insulin sensitivity was assessed by an euglycemic clamp. Participants were matched for aerobic capacity and performed a single 48 min bout of exercise with sets at 70 and 90% of maximum heart rate. Muscle biopsies were obtained at resting conditions, 30 min and 24 h after exercise. Global proteomics analysis identified differentially abundant proteins in muscle. The 5′-UTRs of genes coding for significant proteins were subjected to transcription factor enrichment analysis to identify candidate transcription factors. Q-rt-PCR to determine expression of candidate transcription factors was performed on RNA from resting and post-exercise muscle biopsies; immunoblots quantified protein abundance. RESULTS: Proteins involved in mitochondrial function, protein targeting and translation, and metabolism were among those significantly different between lean and obese groups. Transcription factor enrichment analysis of genes coding for these proteins revealed new candidate transcription factors to be evaluated along the previously identified factors. Q-rt-PCR analysis of RNA and immunoblot analysis from pre- and post-exercise muscle biopsies revealed several transcription and growth factors that had altered responses to exercise in insulin resistant participants. A significant increase (EGR3 and CTGF) and decrease (RELA and ATF2) in the mRNA expression of transcription and growth factors was found after exercise in the lean group, but not in the obese participants. CONCLUSIONS: These results confirm findings of an association between insulin sensitivity and transcription factor mRNA response to exercise and show that obesity also may be a sufficient prerequisite for exercise resistance. Analysis of the muscle proteome together with determination of effects of exercise on expression of transcription factors suggests that abnormal responses of transcription factors to exercise may be responsible for differences in protein abundances in insulin resistant muscle.
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spelling pubmed-80583682021-04-22 Altered Transcription Factor Expression Responses to Exercise in Insulin Resistance Zapata-Bustos, Rocio Finlayson, Jean Langlais, Paul R. Coletta, Dawn K. Luo, Moulun Grandjean, Danielle De Filippis, Elena A. Mandarino, Lawrence Front Physiol Physiology PURPOSE: Insulin resistant muscle is resistant to gene expression changes induced by acute exercise. This study was undertaken to identify transcription factors that differentially respond to exercise in insulin resistance. Candidate transcription factors were identified from analysis of 5′-untranslated regions (5′-UTRs) of exercise responsive genes and from analysis of the 5′-UTRs of genes coding for proteins that differ in abundance in insulin resistance. RESEARCH DESIGN AND METHODS: Twenty participants took part in this study. Insulin sensitivity was assessed by an euglycemic clamp. Participants were matched for aerobic capacity and performed a single 48 min bout of exercise with sets at 70 and 90% of maximum heart rate. Muscle biopsies were obtained at resting conditions, 30 min and 24 h after exercise. Global proteomics analysis identified differentially abundant proteins in muscle. The 5′-UTRs of genes coding for significant proteins were subjected to transcription factor enrichment analysis to identify candidate transcription factors. Q-rt-PCR to determine expression of candidate transcription factors was performed on RNA from resting and post-exercise muscle biopsies; immunoblots quantified protein abundance. RESULTS: Proteins involved in mitochondrial function, protein targeting and translation, and metabolism were among those significantly different between lean and obese groups. Transcription factor enrichment analysis of genes coding for these proteins revealed new candidate transcription factors to be evaluated along the previously identified factors. Q-rt-PCR analysis of RNA and immunoblot analysis from pre- and post-exercise muscle biopsies revealed several transcription and growth factors that had altered responses to exercise in insulin resistant participants. A significant increase (EGR3 and CTGF) and decrease (RELA and ATF2) in the mRNA expression of transcription and growth factors was found after exercise in the lean group, but not in the obese participants. CONCLUSIONS: These results confirm findings of an association between insulin sensitivity and transcription factor mRNA response to exercise and show that obesity also may be a sufficient prerequisite for exercise resistance. Analysis of the muscle proteome together with determination of effects of exercise on expression of transcription factors suggests that abnormal responses of transcription factors to exercise may be responsible for differences in protein abundances in insulin resistant muscle. Frontiers Media S.A. 2021-04-07 /pmc/articles/PMC8058368/ /pubmed/33897458 http://dx.doi.org/10.3389/fphys.2021.649461 Text en Copyright © 2021 Zapata-Bustos, Finlayson, Langlais, Coletta, Luo, Grandjean, De Filippis and Mandarino. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Zapata-Bustos, Rocio
Finlayson, Jean
Langlais, Paul R.
Coletta, Dawn K.
Luo, Moulun
Grandjean, Danielle
De Filippis, Elena A.
Mandarino, Lawrence
Altered Transcription Factor Expression Responses to Exercise in Insulin Resistance
title Altered Transcription Factor Expression Responses to Exercise in Insulin Resistance
title_full Altered Transcription Factor Expression Responses to Exercise in Insulin Resistance
title_fullStr Altered Transcription Factor Expression Responses to Exercise in Insulin Resistance
title_full_unstemmed Altered Transcription Factor Expression Responses to Exercise in Insulin Resistance
title_short Altered Transcription Factor Expression Responses to Exercise in Insulin Resistance
title_sort altered transcription factor expression responses to exercise in insulin resistance
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8058368/
https://www.ncbi.nlm.nih.gov/pubmed/33897458
http://dx.doi.org/10.3389/fphys.2021.649461
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