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Circadian regulation of protein cargo in extracellular vesicles

The circadian clock controls many aspects of physiology, but it remains undescribed whether extracellular vesicles (EVs), including exosomes, involved in cell-cell communications between tissues are regulated in a circadian pattern. We demonstrate a 24-hour rhythmic abundance of individual proteins...

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Autores principales: Yeung, Ching-Yan Chloé, Dondelinger, Frank, Schoof, Erwin M., Georg, Birgitte, Lu, Yinhui, Zheng, Zhiyong, Zhang, Jingdong, Hannibal, Jens, Fahrenkrug, Jan, Kjaer, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993114/
https://www.ncbi.nlm.nih.gov/pubmed/35394844
http://dx.doi.org/10.1126/sciadv.abc9061
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author Yeung, Ching-Yan Chloé
Dondelinger, Frank
Schoof, Erwin M.
Georg, Birgitte
Lu, Yinhui
Zheng, Zhiyong
Zhang, Jingdong
Hannibal, Jens
Fahrenkrug, Jan
Kjaer, Michael
author_facet Yeung, Ching-Yan Chloé
Dondelinger, Frank
Schoof, Erwin M.
Georg, Birgitte
Lu, Yinhui
Zheng, Zhiyong
Zhang, Jingdong
Hannibal, Jens
Fahrenkrug, Jan
Kjaer, Michael
author_sort Yeung, Ching-Yan Chloé
collection PubMed
description The circadian clock controls many aspects of physiology, but it remains undescribed whether extracellular vesicles (EVs), including exosomes, involved in cell-cell communications between tissues are regulated in a circadian pattern. We demonstrate a 24-hour rhythmic abundance of individual proteins in small EVs using liquid chromatography–mass spectrometry in circadian-synchronized tendon fibroblasts. Furthermore, the release of small EVs enriched in RNA binding proteins was temporally separated from those enriched in cytoskeletal and matrix proteins, which peaked during the end of the light phase. Last, we targeted the protein sorting mechanism in the exosome biogenesis pathway and established (by knockdown of circadian-regulated flotillin-1) that matrix metalloproteinase 14 abundance in tendon fibroblast small EVs is under flotillin-1 regulation. In conclusion, we have identified proteomic time signatures for small EVs released by tendon fibroblasts, which supports the view that the circadian clock regulates protein cargo in EVs involved in cell-cell cross-talk.
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spelling pubmed-89931142022-04-22 Circadian regulation of protein cargo in extracellular vesicles Yeung, Ching-Yan Chloé Dondelinger, Frank Schoof, Erwin M. Georg, Birgitte Lu, Yinhui Zheng, Zhiyong Zhang, Jingdong Hannibal, Jens Fahrenkrug, Jan Kjaer, Michael Sci Adv Biomedicine and Life Sciences The circadian clock controls many aspects of physiology, but it remains undescribed whether extracellular vesicles (EVs), including exosomes, involved in cell-cell communications between tissues are regulated in a circadian pattern. We demonstrate a 24-hour rhythmic abundance of individual proteins in small EVs using liquid chromatography–mass spectrometry in circadian-synchronized tendon fibroblasts. Furthermore, the release of small EVs enriched in RNA binding proteins was temporally separated from those enriched in cytoskeletal and matrix proteins, which peaked during the end of the light phase. Last, we targeted the protein sorting mechanism in the exosome biogenesis pathway and established (by knockdown of circadian-regulated flotillin-1) that matrix metalloproteinase 14 abundance in tendon fibroblast small EVs is under flotillin-1 regulation. In conclusion, we have identified proteomic time signatures for small EVs released by tendon fibroblasts, which supports the view that the circadian clock regulates protein cargo in EVs involved in cell-cell cross-talk. American Association for the Advancement of Science 2022-04-08 /pmc/articles/PMC8993114/ /pubmed/35394844 http://dx.doi.org/10.1126/sciadv.abc9061 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Yeung, Ching-Yan Chloé
Dondelinger, Frank
Schoof, Erwin M.
Georg, Birgitte
Lu, Yinhui
Zheng, Zhiyong
Zhang, Jingdong
Hannibal, Jens
Fahrenkrug, Jan
Kjaer, Michael
Circadian regulation of protein cargo in extracellular vesicles
title Circadian regulation of protein cargo in extracellular vesicles
title_full Circadian regulation of protein cargo in extracellular vesicles
title_fullStr Circadian regulation of protein cargo in extracellular vesicles
title_full_unstemmed Circadian regulation of protein cargo in extracellular vesicles
title_short Circadian regulation of protein cargo in extracellular vesicles
title_sort circadian regulation of protein cargo in extracellular vesicles
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993114/
https://www.ncbi.nlm.nih.gov/pubmed/35394844
http://dx.doi.org/10.1126/sciadv.abc9061
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