Loss of 15-lipoxygenase disrupts Treg differentiation altering their pro-resolving functions

Regulatory T-cells (T-regs) are central in the maintenance of homeostasis and resolution of inflammation. However, the mechanisms that govern their differentiation and function are not completely understood. Herein, we demonstrate a central role for the lipid mediator biosynthetic enzyme 15-lipoxygenase (ALOX15) in regulating key aspects of T-reg biology. Pharmacological inhibition or genetic deletion of ALOX15 in T-regs decreased FOXP3 expression, altered T-reg transcriptional profile and shifted their metabolism. This was linked with an impaired ability of Alox15-deficient cells to exert their pro-resolving actions, including a decrease in their ability to upregulate macrophage efferocytosis and a downregulation of interferon gamma expression in Th1 cells. Incubation of T-regs with the ALOX15-derived specilized pro-resolving mediators (SPM)s Resolvin (Rv)D3 and RvD5(n-3 DPA) rescued FOXP3 expression in cells where ALOX15 activity was inhibited. In vivo, deletion of Alox15 led to increased vascular lipid load and expansion of Th1 cells in mice fed western diet, a phenomenon that was reversed when Alox15-deficient mice were reconstituted with wild type T-regs. Taken together these findings demonstrate a central role of pro-resolving lipid mediators in governing the differentiation of naive T-cells to T-regs.

Automated summary

Regulatory T-cells play a central role in maintaining homeostasis and resolving inflammation. ALOX15 was found to regulate key aspects of T-reg biology, with its inhibition or deletion leading to altered gene expression and metabolism in T-regs. Incubation with ALOX15-derived pro-resolving mediators rescued the expression of key regulatory genes in T-regs with inhibited ALOX15 activity.