ERKs induce expression of the transcriptional repressor Blimp-1 and subsequent plasma cell differentiation

Sci Signal. 2011 Apr 19;4(169):ra25. doi: 10.1126/scisignal.2001592.

Abstract

In immune cells, the positive role of the extracellular signal-regulated kinase (ERK) signaling pathway in cell cycle progression and survival is well established; however, it is unclear whether ERK signaling plays a role in cell differentiation. Here, we report that ERKs are essential for the differentiation of B cells into antibody-producing plasma cells and that ERKs induce the expression of Prdm1, which encodes Blimp-1, a transcriptional repressor and "master regulator" of plasma cell differentiation. Transgenic mice with conditional deletion of both ERK1 and ERK2 in germinal center (GC) B cells lacked plasma cells differentiated after GC formation, and memory B cells from these mice failed to differentiate into plasma cells. In addition, ERK1- and ERK2-deficient B cells exhibited impaired Prdm1 expression upon stimulation with antibody against CD40 in the presence of interleukin-4; conversely, enforced expression of Prdm1 in ERK1- and ERK2-deficient B cells restored the generation of plasma cells. Thus, our study suggests that cytokines stimulate ERKs to induce the production of Blimp-1 and that ERKs thereby contribute to the process of cellular differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes / cytology
  • B-Lymphocytes / immunology*
  • Blotting, Western
  • Cell Differentiation / immunology*
  • DNA Primers / genetics
  • Enzyme-Linked Immunosorbent Assay
  • Enzyme-Linked Immunospot Assay
  • Extracellular Signal-Regulated MAP Kinases / genetics
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • Flow Cytometry / methods
  • Germinal Center / metabolism
  • Mice
  • Mice, Transgenic
  • Plasma Cells / cytology*
  • Positive Regulatory Domain I-Binding Factor 1
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction / immunology*
  • Transcription Factors / metabolism

Substances

  • DNA Primers
  • Prdm1 protein, mouse
  • Transcription Factors
  • Positive Regulatory Domain I-Binding Factor 1
  • Extracellular Signal-Regulated MAP Kinases