L-Phenylalanine is a metabolic checkpoint of human Th2 cells

Author:

Kulkarni Abhijeet JORCID,Rodriguez-Coira Juan,Stocker Nino,Radzikowska UrszulaORCID,García-Cívico Antonio JORCID,Delgado Dolset María IsabelORCID,Contreras NuriaORCID,Jardón Parages Inés,Saiz Sanchez Vanessa,Serrano Pilar,Izquierdo Elena,Gomez-Casado Cristina,Sanchez-Solares Javier,Pablo-Torres Carmela,Obeso David,Moreno-Aguilar Carmen,Luisa Espinazo Maria,Eljaszewicz Andrzej,Koch JanaORCID,Baerenfaller KatjaORCID,Heider Anja,Tan Ge,Escribese Maria MORCID,Ruiz-Leon Berta,Akdis Cezmi A,Argüello Rafael J.ORCID,Barber Domingo,Villaseñor AlmaORCID,Sokolowska Milena

Abstract

SummaryAfter the primary response, circulating memory CD4+T effector and T regulatory cells (Treg) regulate recall responses, which are impaired in allergy. Using mass spectrometry, we discovered distinct metabolomes of these cells in humans and their unique enrichment in amino acids. By assessing energy metabolism inin vitroandex vivosingle-cell analyses, we determined that increased intracellular L-phenylalanine boosts glycolysis while limiting OXPHOS in CD4+T, memory CD4+T and Th2, but not in Treg cells. L-phenylalanine also restrains memory CD4+T proliferation in an IL4I1-dependent manner and inhibits Th2 cell proliferation and differentiation. RNA-sequencing, metabolomics, flow cytometry and proteomics, validatedin vitroand across patients’ cohorts, revealed an impairment in LAT1-dependent transport of L-phenylalanine into Th2 cells in allergy with an increase in its intracellular processing, accompanied by an expansion of pathogenic Th2 cells. Thus, our study identifies L-phenylalanine as a checkpoint in the development, energy metabolism and function of Th2 cells.

Publisher

Cold Spring Harbor Laboratory

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