Genomic definition of multiple ex vivo Treg sub-phenotypes
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ABSTRACT: Regulatory T (Treg) cells that express the FoxP3 transcription factor are essential for lymphoid homeostasis and immune tolerance to self. Other non-immunological functions of Treg cells, such as controlling metabolic function in adipose tissue, are also emerging. Treg cells originate primarily in the thymus, but can also be elicited from conventional T cells by in vivo exposure to low-dose antigen or homeostatic expansion, or by activation in the presence of TGFβ in vitro. Treg cells are characterized by a distinct transcriptional signature controlled in part, but not solely, by FoxP3. For a better perspective on transcriptional control in Treg cells, we compared gene expression profiles of a broad panel of Treg cells from various origins or anatomical locations. Treg cells generated by
ORGANISM(S): Mus musculus
SUBMITTER: Christophe Benoist
PROVIDER: E-GEOD-20366 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
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