PLoS ONE (Jan 2013)

The kinase PDK1 is essential for B-cell receptor mediated survival signaling.

  • Sung-Gyoo Park,
  • Meixiao Long,
  • Jung-Ah Kang,
  • Woo-Seok Kim,
  • Cho-Rong Lee,
  • Sin-Hyeog Im,
  • Ian Strickland,
  • Jan Schulze-Luehrmann,
  • Matthew S Hayden,
  • Sankar Ghosh

DOI
https://doi.org/10.1371/journal.pone.0055378
Journal volume & issue
Vol. 8, no. 2
p. e55378

Abstract

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Phosphoinositide-dependent kinase 1 (PDK1) plays an important role in integrating the T cell antigen receptor (TCR) and CD28 signals to achieve efficient NF-κB activation. PDK1 is also an important regulator of T cell development, mediating pre-TCR induced proliferation signals. However, the role of PDK1 in B cell antigen receptor (BCR) signaling and B cell development remains largely unknown. In this study we provide genetic evidence supporting the role of PDK1 in B cell survival. We found PDK1 is required for BCR mediated survival in resting B cells, likely through regulation of Foxo activation. PDK1-dependent signaling to NF-κB is not crucial to resting B cell viability. However, PDK1 is necessary for triggering NF-κB during B cell activation and is required for activated B cell survival. Together these studies demonstrate that PDK1 is essential for BCR-induced signal transduction to Foxo and NF-κB and is indispensable for both resting and activated B cell survival.