Role of IκB kinase β in regulating the remodeling of the CARMA1-Bcl10-MALT1 complex

Biochem Biophys Res Commun. 2018 Jun 2;500(2):268-274. doi: 10.1016/j.bbrc.2018.04.057. Epub 2018 Apr 14.

Abstract

The current work investigates the notion that inducible clustering of signaling mediators of the IKK pathway is important for platelet activation. Thus, while the CARMA1, Bcl10, and MALT1 (CBM) complex is essential for triggering IKK/NF-κB activation upon platelet stimulation, the signals that elicit its formation and downstream effector activation remain elusive. We demonstrate herein that IKKβ is involved in membrane fusion, and serves as a critical protein kinase required for initial formation and the regulation of the CARMA1/MALT1/Bcl10/CBM complex in platelets. We also show that IKKβ regulates these processes via modulation of phosphorylation of Bcl10 and IKKγ polyubiquitination. Collectively, our data demonstrate that IKKβ regulates membrane fusion and the remodeling of the CBM complex formation.

Keywords: CBM complex; IKKβ; SNARE machinery; Ubiquitination.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • B-Cell CLL-Lymphoma 10 Protein / metabolism*
  • Blood Platelets / metabolism
  • Blood Platelets / ultrastructure
  • CARD Signaling Adaptor Proteins / metabolism*
  • Gene Deletion
  • I-kappa B Kinase / metabolism*
  • Membrane Fusion
  • Mice
  • Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein / metabolism*
  • Phosphorylation
  • Protein Kinase C-delta / metabolism
  • Ubiquitination

Substances

  • B-Cell CLL-Lymphoma 10 Protein
  • Bcl10 protein, mouse
  • CARD Signaling Adaptor Proteins
  • Card11 protein, mouse
  • I-kappa B Kinase
  • Protein Kinase C-delta
  • Malt1 protein, mouse
  • Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein