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

Raquel M. Marques,Mauro Perretti,Trinidad Montero-Melendez,Romain A. Colas,Jesmond Dalli,Maria Gonzalez-Nunez,Mary E. Walker,Esteban A. Gomez

doi:10.1038/s41418-021-00807-x

Raquel M. Marques, Mauro Perretti + Show 6 more

Open Access

https://doi.org/10.1038/s41418-021-00807-x

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Abstract

Regulatory T-cells (Tregs) 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 Treg biology. Pharmacological inhibition or genetic deletion of ALOX15 in Tregs decreased FOXP3 expression, altered Treg 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 Tregs with the ALOX15-derived specilized pro-resolving mediators (SPM)s Resolvin (Rv)D3 and RvD5n-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 Tregs. Taken together these findings demonstrate a central role of pro-resolving lipid mediators in governing the differentiation of naive T-cells to Tregs.

Highlights

Regulatory T-cells (Tregs) are a subset of T-cells that play a central role in the maintenance of homeostasis
Similar observations were made in murine Tregs where we observed an upregulation of ALOX5, and ALOX15 in Tregs when compared with naïve CD4+ T-cells (Supplementary Fig. S2)
Given the central role that ALOX15 plays in lipid mediator biosynthesis [15, 18, 19], we assessed the time course for ALOX15 upregulation in relation to FOXP3 expression during the course of Treg differentiation

Summary

Introduction

Regulatory T-cells (Tregs) are a subset of T-cells that play a central role in the maintenance of homeostasis. Defects in Tregs differentiation and/or function are linked with dysregulated lymphoproliferation, autoimmune diseases and chronic inflammation, including atherosclerosis [1,2,3,4]. This is because Tregs are tasked with preventing the unregulated activation of cells within both the innate and adaptive arms of the immune system [1,2,3,4].

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