Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Brown Adipose Tissue Harbors a distinct subpopulation of regulatory T cells


ABSTRACT: Regulatory T (Treg) cells are critical determinants of both immune responses and metabolic control. Here we show that systemic ablation of Treg cells compromised the adaptation of whole-body energy expenditure to cold exposure, correlating with impairment in thermogenic marker gene expression and massive invasion of pro-inflammatory macrophages in brown adipose tissue (BAT). Indeed, BAT harbored a unique sub-set of Treg cells characterized by a unique gene signature. As these Treg cells respond to BAT activation upon cold exposure, this study defines a BAT-specific Treg sub-set with direct implications for the regulation of energy homeostasis in response to environmental stress. We isolated regulatory and conventional T cells from brown-adipose tissue of warm-conditioned or cold-conditioned mice. As controls, we harvested spleen-Treg and Tconv cells from warm-treated mice. Cells were isolated pooled organs and target cells purified by FACS. RNA was extracted and gene expression measured.

ORGANISM(S): Mus musculus

SUBMITTER: Markus Feuerer 

PROVIDER: E-GEOD-64909 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Regulatory T (Treg) cells are critical determinants of both immune responses and metabolic control. Here we show that systemic ablation of Treg cells compromised the adaptation of whole-body energy expenditure to cold exposure, correlating with impairment in thermogenic marker gene expression and massive invasion of pro-inflammatory macrophages in brown adipose tissue (BAT). Indeed, BAT harbored a unique sub-set of Treg cells characterized by a unique gene signature. As these Treg cells respond  ...[more]

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