PRMT5 is essential for B cell development and germinal center dynamics

Nat Commun. 2019 Jan 3;10(1):22. doi: 10.1038/s41467-018-07884-6.

Abstract

Mechanisms regulating B cell development, activation, education in the germinal center (GC) and differentiation, underpin the humoral immune response. Protein arginine methyltransferase 5 (Prmt5), which catalyzes most symmetric dimethyl arginine protein modifications, is overexpressed in B cell lymphomas but its function in normal B cells is poorly defined. Here we show that Prmt5 is necessary for antibody responses and has essential but distinct functions in all proliferative B cell stages in mice. Prmt5 is necessary for B cell development by preventing p53-dependent and p53-independent blocks in Pro-B and Pre-B cells, respectively. By contrast, Prmt5 protects, via p53-independent pathways, mature B cells from apoptosis during activation, promotes GC expansion, and counters plasma cell differentiation. Phenotypic and RNA-seq data indicate that Prmt5 regulates GC light zone B cell fate by regulating transcriptional programs, achieved in part by ensuring RNA splicing fidelity. Our results establish Prmt5 as an essential regulator of B cell biology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / immunology
  • B-Lymphocytes / immunology
  • B-Lymphocytes / metabolism
  • B-Lymphocytes / physiology*
  • Cell Differentiation / immunology
  • Cell Proliferation / physiology*
  • Cells, Cultured
  • Disease Models, Animal
  • Female
  • Gene Knockdown Techniques
  • Germinal Center / cytology
  • Germinal Center / physiology*
  • Humans
  • Immunity, Humoral / physiology*
  • Lymphocyte Activation / immunology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Primary Cell Culture
  • Protein-Arginine N-Methyltransferases / genetics
  • Protein-Arginine N-Methyltransferases / metabolism
  • Protein-Arginine N-Methyltransferases / physiology*
  • Signal Transduction / physiology
  • Trichostrongyloidea / immunology
  • Trichostrongyloidiasis / immunology
  • Trichostrongyloidiasis / parasitology
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Tumor Suppressor Protein p53
  • Prmt5 protein, mouse
  • Protein-Arginine N-Methyltransferases