Selective degradation of PU.1 during autophagy represses the differentiation and antitumour activity of TH9 cells.

Fiche publication


Date publication

septembre 2017

Journal

Nature communications

Auteurs

Membres identifiés du Cancéropôle Est :
Pr GHIRINGHELLI François


Tous les auteurs :
Rivera Vargas T, Cai Z, Shen Y, Dosset M, Benoit-Lizon I, Martin T, Roussey A, Flavell RA, Ghiringhelli F, Apetoh L

Résumé

Autophagy, a catabolic mechanism that involves degradation of cellular components, is essential for cell homeostasis. Although autophagy favours the lineage stability of regulatory T cells, the contribution of autophagy to the differentiation of effector CD4 T cells remains unclear. Here we show that autophagy selectively represses T helper 9 (TH9) cell differentiation. CD4 T cells lacking Atg3 or Atg5 have increased interleukin-9 (IL-9) expression upon differentiation into TH9 cells relative to Atg3- or Atg5-expressing control cells. In addition, the TH9 cell transcription factor, PU.1, undergoes K63 ubiquitination and degradation through p62-dependent selective autophagy. Finally, the blockade of autophagy enhances TH9 cell anticancer functions in vivo, and mice with T cell-specific deletion of Atg5 have reduced tumour outgrowth in an IL-9-dependent manner. Overall, our findings reveal an unexpected function of autophagy in the modulation of TH9 cell differentiation and antitumour activity, and prompt potential autophagy-dependent modulations of TH9 activity for cancer immunotherapy.Autophagy is a cellular process for recycling cell constituents, and is essential for T cell activation, but its function in T cell polarization is still unclear. Here the authors show that autophagy induces the degradation of transcription factor PU.1 to negatively modulate TH9 homeostasis and antitumour immunity.

Mots clés

Animals, Autophagy, immunology, Autophagy-Related Protein 5, Autophagy-Related Proteins, Cell Differentiation, immunology, Immunotherapy, Interleukin-9, immunology, Lymphopoiesis, immunology, Mice, Neoplasms, immunology, Proto-Oncogene Proteins, metabolism, T-Lymphocyte Subsets, immunology, T-Lymphocytes, Helper-Inducer, immunology, Trans-Activators, metabolism, Ubiquitin-Conjugating Enzymes

Référence

Nat Commun. 2017 Sep;8(1):559