Royal College of Surgeons in Ireland
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Intertwining roles of circadian and metabolic regulation of the innate immune response

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posted on 2024-01-18, 14:59 authored by Shannon Cox, James O'Siorain, Lauren FaganLauren Fagan, Annie CurtisAnnie Curtis, Richard G Carroll
It has emerged that an interconnected relationship exists between metabolism, circadian rhythms, and the immune system. The relationship between metabolism and circadian rhythms is not that surprising given the necessity to align rhythms of feeding/fasting with activity/rest. Recently, our understanding of the importance of metabolic pathways in terms of immune function, termed immunometabolism, has grown exponentially. It is now appreciated that the time of day during which the innate immune system is challenged strongly conditions the subsequent response. Recent observations have found that many individual components that make up the circadian clock also control aspects of metabolism in innate immune cells to modulate inflammation. This circadian/metabolic axis may be a key factor driving rhythmicity of immune function and circadian disruption is associated with a range of chronic inflammatory diseases such as atherosclerosis, obesity, and diabetes. The field of “circadian immunometabolism” seeks to reveal undiscovered circadian controlled metabolic pathways that in turn regulate immune responses. The innate immune system has been intricately linked to chronic inflammatory diseases, and within the immune system, individual cell types carry out unique roles in inflammation. Therefore, circadian immunometabolism effects are unique to each innate immune cell.

Funding

Science Foundation Ireland Career Development Award (17/CDA/4688)

Irish Research Council Laureate Award (IRCLA/2017/110)

History

Comments

The original article is available at https://link.springer.com/

Published Citation

Cox SL, O'Siorain JR, Fagan LE, Curtis AM, Carroll RG. Intertwining roles of circadian and metabolic regulation of the innate immune response. Semin Immunopathol. 2022;44(2):225-237.

Publication Date

12 January 2022

PubMed ID

35022891

Department/Unit

  • School of Pharmacy and Biomolecular Sciences
  • Tissue Engineering Research Group (TERG)

Research Area

  • Vascular Biology
  • Immunity, Infection and Inflammation
  • Biomaterials and Regenerative Medicine

Publisher

Springer Science and Business Media LLC

Version

  • Accepted Version (Postprint)