Feuerer, M. et al. Lean, but not obese, fat is enriched for a unique population of regulatory T cells that affect metabolic parameters. Nat. Med. 15, 930-939

Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Joslin Diabetes Center, Boston, Massachusetts, USA.
Nature medicine (Impact Factor: 27.36). 09/2009; 15(8):930-9. DOI: 10.1038/nm.2002
Source: PubMed


Obesity is accompanied by chronic, low-grade inflammation of adipose tissue, which promotes insulin resistance and type-2 diabetes. These findings raise the question of how fat inflammation can escape the powerful armamentarium of cells and molecules normally responsible for guarding against a runaway immune response. CD4(+) Foxp3(+) T regulatory (T(reg)) cells with a unique phenotype were highly enriched in the abdominal fat of normal mice, but their numbers were strikingly and specifically reduced at this site in insulin-resistant models of obesity. Loss-of-function and gain-of-function experiments revealed that these T(reg) cells influenced the inflammatory state of adipose tissue and, thus, insulin resistance. Cytokines differentially synthesized by fat-resident regulatory and conventional T cells directly affected the synthesis of inflammatory mediators and glucose uptake by cultured adipocytes. These observations suggest that harnessing the anti-inflammatory properties of T(reg) cells to inhibit elements of the metabolic syndrome may have therapeutic potential.

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Available from: Jongsoon Lee, Sep 29, 2015
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    • "We therefore examined T cell populations in adipose tissue (Figure S3C). Consistent with previous reports (Feuerer et al., 2009; Nishimura et al., 2009; Winer et al., 2009), within the CD3 + gated T cell population there was an marked increase in the proportion of CD8 + T cells and partial decrease in CD4 + T cells in epididymal adipose tissue of HFD-fed WT mice (Figure 4E). "
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