Mucosal-associated invariant T cells promote inflammation and intestinal dysbiosis leading to metabolic dysfunction during obesity.
Amine ToubalBadr KiafLucie BeaudoinLucie CagninacciMoez RhimiBlandine FruchetJennifer da SilvaAlexandra J CorbettYannick SimoniOlivier LantzJamie RossjohnJames McCluskeyPhilippe LesnikEmmanuelle MaguinAgnès LehuenPublished in: Nature communications (2020)
Obesity is associated with low-grade chronic inflammation promoting insulin-resistance and diabetes. Gut microbiota dysbiosis is a consequence as well as a driver of obesity and diabetes. Mucosal-associated invariant T cells (MAIT) are innate-like T cells expressing a semi-invariant T cell receptor restricted to the non-classical MHC class I molecule MR1 presenting bacterial ligands. Here we show that during obesity MAIT cells promote inflammation in both adipose tissue and ileum, leading to insulin resistance and impaired glucose and lipid metabolism. MAIT cells act in adipose tissue by inducing M1 macrophage polarization in an MR1-dependent manner and in the gut by inducing microbiota dysbiosis and loss of gut integrity. Both MAIT cell-induced tissue alterations contribute to metabolic dysfunction. Treatment with MAIT cell inhibitory ligand demonstrates its potential as a strategy against inflammation, dysbiosis and metabolic disorders.
Keyphrases
- insulin resistance
- adipose tissue
- oxidative stress
- type diabetes
- high fat diet induced
- induced apoptosis
- metabolic syndrome
- high fat diet
- low grade
- glycemic control
- skeletal muscle
- polycystic ovary syndrome
- diabetic rats
- weight loss
- cell cycle arrest
- single cell
- cardiovascular disease
- immune response
- cell therapy
- magnetic resonance
- weight gain
- magnetic resonance imaging
- stem cells
- blood glucose
- computed tomography
- blood pressure
- cell death
- endothelial cells
- fatty acid
- body mass index
- physical activity
- pi k akt
- binding protein
- endoplasmic reticulum stress