Abstract

The thymus is a primary lymphoid organ, home of maturation and selection of thymocytes for generation of functional T-cells. Multiple factors are involved throughout the different stages of the maturation process to tightly regulate T-cell production. The metabolism of arachidonic acid by cyclooxygenases, lipoxygenases and specific isomerases generates eicosanoids, lipid mediators capable of triggering cellular responses. In this study, we determined the profile of expression of the eicosanoids present in the mouse thymus at different stages of thymocyte development. As the group IVA cytosolic phospholipase A2 (cPLA2α) catalyzes the hydrolysis of phospholipids, thereby generating arachidonic acid, we further verified its contribution by including cPLA2α deficient mice to our investigations. We found that a vast array of eicosanoids is expressed in the thymus, which expression is substantially modulated through thymocyte development. The cPLA2α was dispensable in the generation of most eicosanoids in the thymus and consistently, the ablation of the cPLA2α gene in mouse thymus and the culture of thymuses from human newborns in presence of the cPLA2α inhibitor pyrrophenone did not impact thymocyte maturation. This study provides information on the eicosanoid repertoire present during thymocyte development and suggests that thymocyte maturation can occur independently of cPLA2α.

Highlights

  • The thymus has a central role in the immune system as it supports the development, the differentiation and the selection of T-cells [1,2,3]

  • To determine the eicosanoids produced by the thymus through different stages of thymocyte maturation, we compared the lipid profile generated in Fetal thymic organ cultures (FTOC) supernatants (E15.5) after 1, 3 and 5 days of culture

  • We found that LTB4 remains among the most abundant lipid mediator present in the thymus, followed by LXA4 and 5-Hydroxyeicosatetraenoic acid (HETE) (Fig 1C)

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Summary

Introduction

The thymus has a central role in the immune system as it supports the development, the differentiation and the selection of T-cells [1,2,3]. Thymic development of the T-cell precursors is finely regulated. The T-cell precursors originating from the bone marrow enter in the thymus through the cortex. These immature T-cells, called thymocytes, differently express the T-cell receptor (TCR) co-receptors CD4 and CD8 at their surface, an indication of the T-cell maturation state. Owing to the lack of expression of CD4 and CD8 immediately after their.

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