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Insulin/IGF-1 Drives PERIOD Synthesis to Entrain Circadian Rhythms with Feeding Time
In mammals, endogenous circadian clocks sense and respond to daily feeding and lighting cues, adjusting internal ∼24 h rhythms to resonate with, and anticipate, external cycles of day and night. The mechanism underlying circadian entrainment to feeding time is critical for understanding why mistimed...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6506277/ https://www.ncbi.nlm.nih.gov/pubmed/31030999 http://dx.doi.org/10.1016/j.cell.2019.02.017 |
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author | Crosby, Priya Hamnett, Ryan Putker, Marrit Hoyle, Nathaniel P. Reed, Martin Karam, Carolyn J. Maywood, Elizabeth S. Stangherlin, Alessandra Chesham, Johanna E. Hayter, Edward A. Rosenbrier-Ribeiro, Lyn Newham, Peter Clevers, Hans Bechtold, David A. O’Neill, John S. |
author_facet | Crosby, Priya Hamnett, Ryan Putker, Marrit Hoyle, Nathaniel P. Reed, Martin Karam, Carolyn J. Maywood, Elizabeth S. Stangherlin, Alessandra Chesham, Johanna E. Hayter, Edward A. Rosenbrier-Ribeiro, Lyn Newham, Peter Clevers, Hans Bechtold, David A. O’Neill, John S. |
author_sort | Crosby, Priya |
collection | PubMed |
description | In mammals, endogenous circadian clocks sense and respond to daily feeding and lighting cues, adjusting internal ∼24 h rhythms to resonate with, and anticipate, external cycles of day and night. The mechanism underlying circadian entrainment to feeding time is critical for understanding why mistimed feeding, as occurs during shift work, disrupts circadian physiology, a state that is associated with increased incidence of chronic diseases such as type 2 (T2) diabetes. We show that feeding-regulated hormones insulin and insulin-like growth factor 1 (IGF-1) reset circadian clocks in vivo and in vitro by induction of PERIOD proteins, and mistimed insulin signaling disrupts circadian organization of mouse behavior and clock gene expression. Insulin and IGF-1 receptor signaling is sufficient to determine essential circadian parameters, principally via increased PERIOD protein synthesis. This requires coincident mechanistic target of rapamycin (mTOR) activation, increased phosphoinositide signaling, and microRNA downregulation. Besides its well-known homeostatic functions, we propose insulin and IGF-1 are primary signals of feeding time to cellular clocks throughout the body. |
format | Online Article Text |
id | pubmed-6506277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-65062772019-05-13 Insulin/IGF-1 Drives PERIOD Synthesis to Entrain Circadian Rhythms with Feeding Time Crosby, Priya Hamnett, Ryan Putker, Marrit Hoyle, Nathaniel P. Reed, Martin Karam, Carolyn J. Maywood, Elizabeth S. Stangherlin, Alessandra Chesham, Johanna E. Hayter, Edward A. Rosenbrier-Ribeiro, Lyn Newham, Peter Clevers, Hans Bechtold, David A. O’Neill, John S. Cell Article In mammals, endogenous circadian clocks sense and respond to daily feeding and lighting cues, adjusting internal ∼24 h rhythms to resonate with, and anticipate, external cycles of day and night. The mechanism underlying circadian entrainment to feeding time is critical for understanding why mistimed feeding, as occurs during shift work, disrupts circadian physiology, a state that is associated with increased incidence of chronic diseases such as type 2 (T2) diabetes. We show that feeding-regulated hormones insulin and insulin-like growth factor 1 (IGF-1) reset circadian clocks in vivo and in vitro by induction of PERIOD proteins, and mistimed insulin signaling disrupts circadian organization of mouse behavior and clock gene expression. Insulin and IGF-1 receptor signaling is sufficient to determine essential circadian parameters, principally via increased PERIOD protein synthesis. This requires coincident mechanistic target of rapamycin (mTOR) activation, increased phosphoinositide signaling, and microRNA downregulation. Besides its well-known homeostatic functions, we propose insulin and IGF-1 are primary signals of feeding time to cellular clocks throughout the body. Cell Press 2019-05-02 /pmc/articles/PMC6506277/ /pubmed/31030999 http://dx.doi.org/10.1016/j.cell.2019.02.017 Text en © 2019 MRC Laboratory of Molecular Biology http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Crosby, Priya Hamnett, Ryan Putker, Marrit Hoyle, Nathaniel P. Reed, Martin Karam, Carolyn J. Maywood, Elizabeth S. Stangherlin, Alessandra Chesham, Johanna E. Hayter, Edward A. Rosenbrier-Ribeiro, Lyn Newham, Peter Clevers, Hans Bechtold, David A. O’Neill, John S. Insulin/IGF-1 Drives PERIOD Synthesis to Entrain Circadian Rhythms with Feeding Time |
title | Insulin/IGF-1 Drives PERIOD Synthesis to Entrain Circadian Rhythms with Feeding Time |
title_full | Insulin/IGF-1 Drives PERIOD Synthesis to Entrain Circadian Rhythms with Feeding Time |
title_fullStr | Insulin/IGF-1 Drives PERIOD Synthesis to Entrain Circadian Rhythms with Feeding Time |
title_full_unstemmed | Insulin/IGF-1 Drives PERIOD Synthesis to Entrain Circadian Rhythms with Feeding Time |
title_short | Insulin/IGF-1 Drives PERIOD Synthesis to Entrain Circadian Rhythms with Feeding Time |
title_sort | insulin/igf-1 drives period synthesis to entrain circadian rhythms with feeding time |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6506277/ https://www.ncbi.nlm.nih.gov/pubmed/31030999 http://dx.doi.org/10.1016/j.cell.2019.02.017 |
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