The proliferation of human mucosal-associated invariant T cells requires a MYC-SLC7A5-glycolysis metabolic axis

Author:

Kedia-Mehta Nidhi1ORCID,Pisarska Marta M.12ORCID,Rollings Christina3,O’Neill Chloe2ORCID,De Barra Conor2ORCID,Foley Cathriona4ORCID,Wood Nicole A. W.12,Wrigley-Kelly Neil56,Veerapen Natacha7,Besra Gurdyal7ORCID,Bergin Ronan2ORCID,Jones Nicholas8ORCID,O’Shea Donal256,Sinclair Linda V.3ORCID,Hogan Andrew E.12ORCID

Affiliation:

1. Kathleen Lonsdale Institute for Human Health Research, Maynooth University, Maynooth, Co Kildare, Ireland.

2. National Children’s Research Centre, Dublin 12, Ireland.

3. Division of Cell Signaling and Immunology, School of Life Sciences, University of Dundee, Dundee, UK.

4. Department of Biological Sciences, Munster Technological University, Cork, Ireland.

5. St. Vincent’s University Hospital, Dublin 4, Ireland.

6. University College Dublin, Dublin 4, Ireland.

7. School of Biosciences, University of Birmingham, Birmingham, UK.

8. Institute of Life Science, Swansea University Medical School, Swansea, UK.

Abstract

Mucosal-associated invariant T (MAIT) cells are an abundant population of innate T cells that recognize bacterial ligands and play a key role in host protection against bacterial and viral pathogens. Upon activation, MAIT cells undergo proliferative expansion and increase their production of effector molecules such as cytokines. In this study, we found that both mRNA and protein abundance of the key metabolism regulator and transcription factor MYC was increased in stimulated MAIT cells. Using quantitative mass spectrometry, we identified the activation of two MYC-controlled metabolic pathways, amino acid transport and glycolysis, both of which were necessary for MAIT cell proliferation. Last, we showed that MAIT cells isolated from people with obesity showed decreased MYC mRNA abundance upon activation, which was associated with defective MAIT cell proliferation and functional responses. Collectively, our data uncover the importance of MYC-regulated metabolism for MAIT cell proliferation and provide additional insight into the molecular basis for the functional defects of MAIT cells in obesity.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Cell Biology,Molecular Biology,Biochemistry

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