Protein Kinase CK2 Regulates B Cell Development and Differentiation. Academic Article uri icon

Overview

abstract

  • Protein kinase CK2 (also known as Casein Kinase 2) is a serine/threonine kinase composed of two catalytic subunits (CK2α and/or CK2α') and two regulatory CK2β subunits. CK2 is overexpressed and overactive in B cell acute lymphoblastic leukemia and diffuse large B cell lymphomas, leading to inappropriate activation of the NF-κB, JAK/STAT, and PI3K/AKT/mTOR signaling pathways and tumor growth. However, whether CK2 regulates normal B cell development and differentiation is not known. We generated mice lacking CK2α specifically in B cells (using CD19-driven Cre recombinase). These mice exhibited cell-intrinsic expansion of marginal zone B cells at the expense of transitional B cells, without changes in follicular B cells. Transitional B cells required CK2α to maintain adequate BCR signaling. In the absence of CK2α, reduced BCR signaling and elevated Notch2 signaling activation increased marginal zone B cell differentiation. Our results identify a previously unrecognized function for CK2α in B cell development and differentiation.

publication date

  • July 23, 2021

Research

keywords

  • B-Lymphocytes
  • Casein Kinase II
  • Precursor Cells, B-Lymphoid

Identity

PubMed Central ID

  • PMC8323969

Scopus Document Identifier

  • 85111710097

Digital Object Identifier (DOI)

  • 10.4049/jimmunol.2100059

PubMed ID

  • 34301844

Additional Document Info

volume

  • 207

issue

  • 3