Targeting IRE1α improves insulin sensitivity and thermogenesis and suppresses metabolically active adipose tissue macrophages in obesity.
Dan WuVenkateswararao EedaZahra MariaKomal RawalOana Herlea-PanaRam Babu UndiHui-Ying LimWeidong WangPublished in: bioRxiv : the preprint server for biology (2024)
Overnutrition engenders the expansion of adipose tissue and the accumulation of immune cells, in particular, macrophages, in the adipose tissue, leading to chronic low-grade inflammation and insulin resistance. In obesity, several proinflammatory subpopulations of adipose tissue macrophages (ATMs) identified hitherto include the conventional "M1-like" CD11C-expressing ATM and the newly discovered metabolically activated CD9-expressing ATM; however, the relationship among ATM subpopulations is unclear. The ER stress sensor inositol-requiring enzyme 1α (IRE1α) is activated in the adipocytes and immune cells under obesity. It is unknown whether targeting IRE1α is capable of reversing insulin resistance and obesity and modulating the metabolically activated ATMs. We report that pharmacological inhibition of IRE1α RNase significantly ameliorates insulin resistance and glucose intolerance in diet-induced obesity mice. IRE1α inhibition also increases thermogenesis and energy expenditure, and hence protects against high fat diet-induced obesity. Our study shows that the "M1-like" CD11c + ATMs are largely overlapping with but yet non-identical to CD9 + ATMs in obese white adipose tissue. Notably, IRE1α inhibition diminishes the accumulation of obesity-induced metabolically activated ATMs and "M1-like" ATMs, resulting in the curtailment of adipose inflammation and ensuing reactivation of thermogenesis, without augmentation of the alternatively activated M2 macrophage population. Our findings suggest the potential of targeting IRE1α for the therapeutic treatment of insulin resistance and obesity.
Keyphrases
- insulin resistance
- adipose tissue
- high fat diet induced
- high fat diet
- polycystic ovary syndrome
- metabolic syndrome
- endoplasmic reticulum stress
- low grade
- type diabetes
- skeletal muscle
- dna damage
- oxidative stress
- dna repair
- smoking cessation
- dna damage response
- risk assessment
- high grade
- blood pressure
- signaling pathway
- drug induced
- climate change