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PPARγ marks splenic precursors of multiple nonlymphoid-tissue Treg compartments

Chaoran Li, Andrés Rojas, Gang Wang, Alexander O. Mann, Christophe Benoıst, Diane Mathis

2021Proceedings of the National Academy of Sciences45 citationsDOIOpen Access PDF

Abstract

Significance Foxp3 + CD4 + regulatory T cells (Tregs) control both immune responses and tissue homeostasis. Dedicated Treg compartments occur in several nonlymphoid tissues—When, where, and how do they acquire specialized characteristics? A splenic Treg population expressing low levels of the transcription factor PPARγ contains precursors of Tregs in visceral adipose tissue. Since PPARγ, the “master regulator” of adipocyte differentiation, is required for the accumulation and function of Tregs in this tissue but not others, its expression in splenic precursors of adipose-tissue Tregs is not surprising. We show that the splenic PPARγ lo Treg population is transcriptionally heterogeneous and engenders Tregs in multiple additional nonlymphoid tissues. A general pool of splenic precursors of nonlymphoid-tissue Tregs opens possibilities for manipulating them experimentally or therapeutically.

Topics & Concepts

Adipose tissueFOXP3PopulationTranscription factorImmune systemBiologyAdipocyteImmunologySpleenRegulatorCell biologyHomeostasisEndocrinologyMedicineGeneBiochemistryEnvironmental healthT-cell and B-cell ImmunologyImmune Cell Function and InteractionAtherosclerosis and Cardiovascular Diseases
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