PTBP1 is necessary for dendritic cells to regulate T-cell homeostasis and antitumour immunity

Immunology. 2021 May;163(1):74-85. doi: 10.1111/imm.13304. Epub 2021 Feb 3.

Abstract

Dendritic cells (DCs) play an important role in linking innate and adaptive immunity. DCs can sense endogenous and exogenous antigens and present those antigens to T cells to induce an immune response or immune tolerance. During activation, alternative splicing (AS) in DCs is dramatically changed to induce cytokine secretion and upregulation of surface marker expression. PTBP1, an RNA-binding protein, is essential in alternative splicing, but the function of PTBP1 in DCs is unknown. Here, we found that a specific deficiency of Ptbp1 in DCs could increase MHC II expression and perturb T-cell homeostasis without affecting DC development. Functionally, Ptbp1 deletion in DCs could enhance antitumour immunity and asthma exacerbation. Mechanistically, we found that Pkm alternative splicing and a subset of Ifn response genes could be regulated by PTBP1. These findings revealed the function of PTBP1 in DCs and indicated that PTBP1 might be a novel therapeutic target for antitumour treatment.

Keywords: RNA-binding protein; alternative splicing; asthma; dendritic cells; tumour.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing
  • Animals
  • Asthma / enzymology*
  • Asthma / genetics
  • Asthma / immunology
  • Asthma / pathology
  • Cell Line, Tumor
  • Cytokines / genetics
  • Cytokines / metabolism
  • Dendritic Cells / enzymology*
  • Dendritic Cells / immunology
  • Gene Expression Regulation
  • Heterogeneous-Nuclear Ribonucleoproteins / genetics
  • Heterogeneous-Nuclear Ribonucleoproteins / metabolism*
  • Histocompatibility Antigens Class II / metabolism
  • Homeostasis
  • Lung / enzymology*
  • Lung / immunology
  • Lung / pathology
  • Lymphocyte Activation
  • Lymphocytes, Tumor-Infiltrating / immunology
  • Lymphocytes, Tumor-Infiltrating / metabolism*
  • Melanoma, Experimental / enzymology*
  • Melanoma, Experimental / genetics
  • Melanoma, Experimental / immunology
  • Melanoma, Experimental / metabolism
  • Mice
  • Mice, Knockout
  • Polypyrimidine Tract-Binding Protein / genetics
  • Polypyrimidine Tract-Binding Protein / metabolism*
  • Pyruvate Kinase / genetics
  • Pyruvate Kinase / metabolism
  • Skin Neoplasms / enzymology*
  • Skin Neoplasms / genetics
  • Skin Neoplasms / immunology
  • Skin Neoplasms / pathology
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism*
  • Tumor Escape
  • Tumor Microenvironment

Substances

  • Cytokines
  • Heterogeneous-Nuclear Ribonucleoproteins
  • Histocompatibility Antigens Class II
  • Ptbp1 protein, mouse
  • Polypyrimidine Tract-Binding Protein
  • Pkm protein, mouse
  • Pyruvate Kinase