ICOS signaling limits regulatory T cell accumulation and function in visceral adipose tissue

A unique population of Foxp3(+) regulatory T cells (T(R)s) resides in visceral adipose tissue (VAT) that regulates adipose inflammation and helps preserve insulin sensitivity. Inducible T cell co-stimulator (ICOS) is highly expressed on effector (e)T(R)s that migrate to nonlymphoid tissues, and contributes to their maintenance and function in models of autoimmunity. In this study, we report an unexpected cell-intrinsic role for ICOS expression and downstream phosphoinositide 3-kinase (PI3K) signaling in limiting the abundance, VAT-associated phenotype, and function of T(R)s specifically in VAT. Icos(−)(/−) mice and mice expressing a knock-in form of ICOS that cannot activate PI3K had increased VAT-T(R) abundance and elevated expression of canonical VAT-T(R) markers. Loss of ICOS signaling facilitated enhanced accumulation of T(R)s to VAT associated with elevated CCR3 expression, and resulted in reduced adipose inflammation and heightened insulin sensitivity in the context of a high-fat diet. Thus, we have uncovered a new and surprising molecular pathway that regulates VAT-T(R) accumulation and function.