Regulation of B cell differentiation by the ubiquitin-binding protein TAX1BP1

نویسندگان

  • Nobuko Matsushita
  • Midori Suzuki
  • Emi Ikebe
  • Shun Nagashima
  • Ryoko Inatome
  • Kenichi Asano
  • Masato Tanaka
  • Masayuki Matsushita
  • Eisaku Kondo
  • Hidekatsu Iha
  • Shigeru Yanagi
چکیده

Tax1-binding protein 1 (TAX1BP1) is a ubiquitin-binding protein that restricts nuclear factor-κB (NF-κB) activation and facilitates the termination of aberrant inflammation. However, its roles in B-cell activation and differentiation are poorly understood. To evaluate the function of TAX1BP1 in B cells, we established TAX1BP1-deficient DT40 B cells that are hyper-responsive to CD40-induced extracellular signal-regulated kinase (ERK) activation signaling, exhibit prolonged and exaggerated ERK phosphorylation and show enhanced B lymphocyte-induced maturation protein 1 (Blimp-1; a transcription factor inducing plasma cell differentiation) expression that is ERK-dependent. Furthermore, TAX1BP1-deficient cells exhibit significantly decreased surface IgM expression and increased IgM secretion. Moreover, TAX1BP1-deficient mice display reduced germinal center formation and antigen-specific antibody production. These findings show that TAX1BP1 restricts ERK activation and Blimp-1 expression and regulates germinal center formation.

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عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2016