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The circadian clock regulates inflammatory arthritis
There is strong diurnal variation in the symptoms and severity of chronic inflammatory diseases, such as rheumatoid arthritis. In addition, disruption of the circadian clock is an aggravating factor associated with a range of human inflammatory diseases. To investigate mechanistic links between the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Federation of American Societies for Experimental Biology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067252/ https://www.ncbi.nlm.nih.gov/pubmed/27488122 http://dx.doi.org/10.1096/fj.201600353R |
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author | Hand, Laura E. Hopwood, Thomas W. Dickson, Suzanna H. Walker, Amy L. Loudon, Andrew S. I. Ray, David W. Bechtold, David A. Gibbs, Julie E. |
author_facet | Hand, Laura E. Hopwood, Thomas W. Dickson, Suzanna H. Walker, Amy L. Loudon, Andrew S. I. Ray, David W. Bechtold, David A. Gibbs, Julie E. |
author_sort | Hand, Laura E. |
collection | PubMed |
description | There is strong diurnal variation in the symptoms and severity of chronic inflammatory diseases, such as rheumatoid arthritis. In addition, disruption of the circadian clock is an aggravating factor associated with a range of human inflammatory diseases. To investigate mechanistic links between the biological clock and pathways underlying inflammatory arthritis, mice were administered collagen (or saline as a control) to induce arthritis. The treatment provoked an inflammatory response within the limbs, which showed robust daily variation in paw swelling and inflammatory cytokine expression. Inflammatory markers were significantly repressed during the dark phase. Further work demonstrated an active molecular clock within the inflamed limbs and highlighted the resident inflammatory cells, fibroblast-like synoviocytes (FLSs), as a potential source of the rhythmic inflammatory signal. Exposure of mice to constant light disrupted the clock in peripheral tissues, causing loss of the nighttime repression of local inflammation. Finally, the results show that the core clock proteins cryptochrome (CRY) 1 and 2 repressed inflammation within the FLSs, and provide novel evidence that a CRY activator has anti-inflammatory properties in human cells. We conclude that under chronic inflammatory conditions, the clock actively represses inflammatory pathways during the dark phase. This interaction has exciting potential as a therapeutic avenue for treatment of inflammatory disease.—Hand, L. E., Hopwood, T. W., Dickson, S. H., Walker, A. L., Loudon, A. S. I., Ray, D. W., Bechtold, D. A., Gibbs, J. E. The circadian clock regulates inflammatory arthritis. |
format | Online Article Text |
id | pubmed-5067252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Federation of American Societies for Experimental Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-50672522016-10-19 The circadian clock regulates inflammatory arthritis Hand, Laura E. Hopwood, Thomas W. Dickson, Suzanna H. Walker, Amy L. Loudon, Andrew S. I. Ray, David W. Bechtold, David A. Gibbs, Julie E. FASEB J Research There is strong diurnal variation in the symptoms and severity of chronic inflammatory diseases, such as rheumatoid arthritis. In addition, disruption of the circadian clock is an aggravating factor associated with a range of human inflammatory diseases. To investigate mechanistic links between the biological clock and pathways underlying inflammatory arthritis, mice were administered collagen (or saline as a control) to induce arthritis. The treatment provoked an inflammatory response within the limbs, which showed robust daily variation in paw swelling and inflammatory cytokine expression. Inflammatory markers were significantly repressed during the dark phase. Further work demonstrated an active molecular clock within the inflamed limbs and highlighted the resident inflammatory cells, fibroblast-like synoviocytes (FLSs), as a potential source of the rhythmic inflammatory signal. Exposure of mice to constant light disrupted the clock in peripheral tissues, causing loss of the nighttime repression of local inflammation. Finally, the results show that the core clock proteins cryptochrome (CRY) 1 and 2 repressed inflammation within the FLSs, and provide novel evidence that a CRY activator has anti-inflammatory properties in human cells. We conclude that under chronic inflammatory conditions, the clock actively represses inflammatory pathways during the dark phase. This interaction has exciting potential as a therapeutic avenue for treatment of inflammatory disease.—Hand, L. E., Hopwood, T. W., Dickson, S. H., Walker, A. L., Loudon, A. S. I., Ray, D. W., Bechtold, D. A., Gibbs, J. E. The circadian clock regulates inflammatory arthritis. Federation of American Societies for Experimental Biology 2016-11 2016-08-03 /pmc/articles/PMC5067252/ /pubmed/27488122 http://dx.doi.org/10.1096/fj.201600353R Text en © The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) (http://creativecommons.org/licenses/by/4.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Hand, Laura E. Hopwood, Thomas W. Dickson, Suzanna H. Walker, Amy L. Loudon, Andrew S. I. Ray, David W. Bechtold, David A. Gibbs, Julie E. The circadian clock regulates inflammatory arthritis |
title | The circadian clock regulates inflammatory arthritis |
title_full | The circadian clock regulates inflammatory arthritis |
title_fullStr | The circadian clock regulates inflammatory arthritis |
title_full_unstemmed | The circadian clock regulates inflammatory arthritis |
title_short | The circadian clock regulates inflammatory arthritis |
title_sort | circadian clock regulates inflammatory arthritis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067252/ https://www.ncbi.nlm.nih.gov/pubmed/27488122 http://dx.doi.org/10.1096/fj.201600353R |
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