Abstract
Obesity-associated inflammation stems from a combination of cell-intrinsic changes of individual immune cell subsets and the dynamic crosstalk amongst a broad array of immune cells. Although much of the focus of immune cell contributions to metabolic disease has focused on adipose tissue-associated cells, these potent sources of inflammation inhabit other metabolic regulatory tissues, including liver and gut, and recirculate to promote systemic inflammation and thus obesity comorbidities. Tissue-associated immune cells, especially T cell subpopulations, have become a hotspot of inquiry based on their contributions to obesity, type 2 diabetes, non-alcoholic fatty liver diseases and certain types of cancers. The cell-cell interactions that take place under the stress of obesity are mediated by intracellular contact and cytokine production, and constitute a complicated network that drives the phenotypic alterations of immune cells and perpetuates a feed-forward loop of metabolic decline. Herein we discuss immune cell functions in various tissues and obesity-associated cancers from the viewpoint of inflammation. We also emphasize recent advances in the understanding of crosstalk amongst immune cell subsets under obese conditions, and suggest future directions for focused investigations with clinical relevance.
Original language | English |
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Article number | 1587 |
Journal | Frontiers in Immunology |
Volume | 10 |
Issue number | JULY |
DOIs | |
State | Published - 2019 |
Bibliographical note
Publisher Copyright:Copyright © 2019 Liu and Nikolajczyk.
Funding
This work was supported by R01DK108056 and R01DE025383. The NIH played no role in the contents of this article.
Funders | Funder number |
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National Institutes of Health (NIH) |
Keywords
- Cancer
- Crosstalk
- Inflammation
- Obesity
- Tissue-specific T cells
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology