Communication Between Natural Killer T Cells and Adipocytes in Obesity
Overview
Endocrinology
Physiology
Authors
Affiliations
Adipose tissue contains various types of immunocompetent cells, and these cells of innate and adaptive immunity control adipose tissue inflammation that blunts insulin sensitivity. Recent studies have shown that adipocytes express CD1d and present lipid antigen(s) to activate natural killer T (NKT) cells. The function of adipocytes is in turn modulated by cytokines that NKT cells produce to alter the expression of anti-inflammatory adipokine(s) and the production of inflammatory and chemoattractant cytokines. These studies imply that the interaction between adipocytes and NKT cells might affect the development of not only obesity but also obesity-related diseases. To test the importance of the interaction between NKT cells and adipocytes, we examined whether an adipocyte-specific CD1d deletion affected the development of obesity, which had been demonstrated with B6.CD1d (CD1d KO). We found that the interaction is indeed important to induce adipose tissue inflammation and insulin resistance in response to lipid excess. In this commentary, the advances and controversies on NKT cells and obesity are discussed based on our recent report that NKT cells play a pivotal role in the regulation of adipose tissue by communicating with adipocytes via CD1d.
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PMID: 38595891 PMC: 11002967. DOI: 10.7759/cureus.55881.
Editorial: Role of CD1- and MR1-Restricted T Cells in Immunity and Disease.
Iwabuchi K, Van Kaer L Front Immunol. 2019; 10:1837.
PMID: 31447847 PMC: 6691045. DOI: 10.3389/fimmu.2019.01837.
The Pathophysiological Relevance of the iNKT Cell/Mononuclear Phagocyte Crosstalk in Tissues.
Cortesi F, Delfanti G, Casorati G, Dellabona P Front Immunol. 2018; 9:2375.
PMID: 30369933 PMC: 6194905. DOI: 10.3389/fimmu.2018.02375.
Zhao Y, Li Z, Yang T, Wang M, Xi X PLoS One. 2018; 13(6):e0198669.
PMID: 29883469 PMC: 5993298. DOI: 10.1371/journal.pone.0198669.
Ren Y, Sekine-Kondo E, Shibata R, Kato-Itoh M, Umino A, Yanagida A Sci Rep. 2017; 7(1):12765.
PMID: 28986544 PMC: 5630609. DOI: 10.1038/s41598-017-12475-4.