Alternative activation of mast cells by CD4+ T helper cells.

Autor: Leveque E; Institut National de la Santé et de la Recherche Médicale, Unité Mixte de Recherche U1037, Centre de Recherche en Cancérologie de Toulouse, 2 Avenue H. Curien, F-31037, France.; Université Toulouse III - Paul Sabatier, 118 route de Narbone, Toulouse F-31062, France., Battut L; Université Toulouse III - Paul Sabatier, 118 route de Narbone, Toulouse F-31062, France.; Institut National de la Santé et de la Recherche Médicale, U1220, Institut de Recherche en Santé Digestive, Institut National de la Recherche Agronomique, Institut National Polytechnique de Toulouse-École Nationale Vétérinaire de Toulouse, CHU Purpan place du Dr Baylac CS 60039, Toulouse F-31024, France., Petitfils C; Université Toulouse III - Paul Sabatier, 118 route de Narbone, Toulouse F-31062, France.; Institut National de la Santé et de la Recherche Médicale, U1220, Institut de Recherche en Santé Digestive, Institut National de la Recherche Agronomique, Institut National Polytechnique de Toulouse-École Nationale Vétérinaire de Toulouse, CHU Purpan place du Dr Baylac CS 60039, Toulouse F-31024, France., Valitutti S; Institut National de la Santé et de la Recherche Médicale, Unité Mixte de Recherche U1037, Centre de Recherche en Cancérologie de Toulouse, 2 Avenue H. Curien, F-31037, France.; Université Toulouse III - Paul Sabatier, 118 route de Narbone, Toulouse F-31062, France.; Department of Pathology, Institut Universitaire du Cancer-Oncopole de Toulouse, Centre Hospitalier Universitaire de Toulouse, 1 avenue Irène Joliot-Curie, Toulouse F-31059, France., Cenac N; Université Toulouse III - Paul Sabatier, 118 route de Narbone, Toulouse F-31062, France.; Institut National de la Santé et de la Recherche Médicale, U1220, Institut de Recherche en Santé Digestive, Institut National de la Recherche Agronomique, Institut National Polytechnique de Toulouse-École Nationale Vétérinaire de Toulouse, CHU Purpan place du Dr Baylac CS 60039, Toulouse F-31024, France., Dietrich G; Université Toulouse III - Paul Sabatier, 118 route de Narbone, Toulouse F-31062, France.; Institut National de la Santé et de la Recherche Médicale, U1220, Institut de Recherche en Santé Digestive, Institut National de la Recherche Agronomique, Institut National Polytechnique de Toulouse-École Nationale Vétérinaire de Toulouse, CHU Purpan place du Dr Baylac CS 60039, Toulouse F-31024, France., Espinosa E; Université Toulouse III - Paul Sabatier, 118 route de Narbone, Toulouse F-31062, France.; Institut National de la Santé et de la Recherche Médicale, U1220, Institut de Recherche en Santé Digestive, Institut National de la Recherche Agronomique, Institut National Polytechnique de Toulouse-École Nationale Vétérinaire de Toulouse, CHU Purpan place du Dr Baylac CS 60039, Toulouse F-31024, France.
Jazyk: angličtina
Zdroj: Journal of leukocyte biology [J Leukoc Biol] 2024 Nov 04; Vol. 116 (5), pp. 1127-1141.
DOI: 10.1093/jleuko/qiae139
Abstrakt: Effector CD4+ T (Teff) lymphocytes infiltrate sites of inflammation and orchestrate the immune response by instructing local leukocytes. Mast cells (MCs) are tissue sentinel cells strategically located near blood vessels and T cell-rich areas. MC/Teff cell interactions shape Teff cell responses, but in turn, Teff cell action on MCs is still poorly understood. Here, we analyzed the human MC/Teff cell interplay through both the application of RNA sequencing and functional assays. We showed that activated Teff cells induce a specific transcriptomic program in MCs including production of both inflammatory cytokines and chemokines, prostaglandin, and a FcεRI-dependent degranulation facilitation, thereby driving them toward an inflammatory phenotype. Moreover, Teff cells induce in MCs the capacity to interact with CD4+ T cells through a wide range of dedicated soluble and membrane ligands and to play the role of antigen-presenting cells.
Competing Interests: Conflict of interest statement. None declared.
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Databáze: MEDLINE