Abstract
Metabolism regulates an array of cellular processes from embryonic development through adulthood. These include proliferation, differentiation and the effector functions of adult cells to maintain homeostasis and repair. It is becoming clear that bioenergetic shifts can control how cells respond to environmental disruptions during tissue injury to initiate a healing response. Specifically, innate immune cells shift their phenotypes to initiate and resolve inflammation, and there is intense interest to understand how these responses might regulate healing outcomes. Here, we review recent literature describing how cellular metabolism and metabolic byproducts regulate phenotype conversions among innate immune cells. Although most studies of this kind do not focus on tissue damage, we discuss how metabolic regulation of these phenotypes promotes tissue repair. In particular, we provide a framework for considering the extent to which altering the innate immune response might shift fibrotic repair towards regenerative healing.
Original language | English |
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Pages (from-to) | 72-82 |
Number of pages | 11 |
Journal | Current Opinion in Immunology |
Volume | 68 |
DOIs | |
State | Published - Feb 2021 |
Bibliographical note
Publisher Copyright:© 2020 Elsevier Ltd
Funding
We would like to thank Emily Johnson for designing figures. We apologize to those authors whose work we could not include due to space limitations. AWS’s lab is supported by grants from NSF ( IOS-1353713 ) and NIH (NIAMS – R01AR070313 and NIDCR – R21DE028070).
Funders | Funder number |
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National Science Foundation Arctic Social Science Program | IOS-1353713 |
National Institutes of Health (NIH) | |
National Institute of Arthritis and Musculoskeletal and Skin Diseases | R01AR070313 |
National Institute of Dental and Craniofacial Research | R21DE028070 |
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology