Key result
Adipose tissue macrophages drive obesity-associated inflammation through diverse subpopulations and extensive cellular crosstalk.
Why the study?
Understanding the pathological mechanisms underlying obesity, including the roles of adipose tissue macrophages beyond classical M1/M2 polarization, is critical for developing new intervention strategies for obesity and its comorbidities.
This review summarizes recent advances in understanding the diverse roles and cellular crosstalk of adipose tissue macrophages in obesity-induced inflammation and insulin resistance.
Highlights macrophage subpopulations as potential targets in obesity inflammation; leaves open clinical translation pending interventional trials.
Obesity has become a worldwide epidemic that poses a severe threat to human health. Evidence suggests that many obesity comorbidities, such as type 2 diabetes mellitus, steatohepatitis, and cardiovascular diseases, are related to obesity-induced chronic low-grade inflammation. Macrophages are the primary immune cells involved in obesity-associated inflammation in both mice and humans. Intensive research over the past few years has yielded tremendous progress in our understanding of the additional roles of adipose tissue macrophages (ATMs) beyond classical M1/M2 polarization in obesity and related comorbidities. In this review, we first characterize the diverse subpopulations of ATMs in the context of obesity. Furthermore, we review the recent advance on the role of the extensive crosstalk between adipocytes and ATMs in obesity. Finally, we focus on the extended crosstalk within adipose tissue between perivascular mesenchymal cells and ATMs. Understanding the pathological mechanisms that underlie obesity will be critical for the development of new intervention strategies to prevent or treat this disease and its associated co-morbidities.
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Cai et al. (2022) conducted a review in Obesity and Insulin Resistance. Adipose tissue macrophages play a critical role in obesity-associated inflammation through diverse subpopulations and extensive crosstalk with adipocytes and perivascular mesenchymal cells.
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