Multiple Roles of Sirtuin 6 in Adipose Tissue Inflammation.

Diabetes Metab J

Department of Biochemistry and Research Institute for Endocrine Sciences, Chonbuk National University Medical School, Jeonju, Korea.

Published: March 2023

AI Article Synopsis

  • - Adipose tissue inflammation is a key factor in obesity-related insulin resistance, where inflamed adipocytes release cytokines that attract immune cells.
  • - Sirtuin 6 (Sirt6) is crucial for regulating this inflammation but its levels drop in obese individuals and rise with weight loss; its deficiency can impact various immune cells and their roles in inflammation.
  • - The review discusses specific immune cell types involved in adipose tissue inflammation and highlights the need for more research on Sirt6's effects on insulin resistance and mechanisms of adipose tissue browning.

Article Abstract

Adipose tissue (AT) inflammation is strongly associated with obesity-induced insulin resistance. When subjected to metabolic stress, adipocytes become inflamed and secrete a plethora of cytokines and chemokines, which recruit circulating immune cells to AT. Although sirtuin 6 (Sirt6) is known to control genomic stabilization, aging, and cellular metabolism, it is now understood to also play a pivotal role in the regulation of AT inflammation. Sirt6 protein levels are reduced in the AT of obese humans and animals and increased by weight loss. In this review, we summarize the potential mechanism of AT inflammation caused by impaired action of Sirt6 from the immune cells' point of view. We first describe the properties and functions of immune cells in obese AT, with an emphasis on discrete macrophage subpopulations which are central to AT inflammation. We then highlight data that links Sirt6 to functional phenotypes of AT inflammation. Importantly, we discuss in detail the effects of Sirt6 deficiency in adipocytes, macrophages, and eosinophils on insulin resistance or AT browning. In our closing perspectives, we discuss emerging issues in this field that require further investigation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10040615PMC
http://dx.doi.org/10.4093/dmj.2022.0270DOI Listing

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