| Literature DB >> 34301844 |
Hairong Wei1, Wei Yang1, Huixian Hong1, Zhaoqi Yan1,2, Hongwei Qin3, Etty N Benveniste1.
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.Entities:
Mesh:
Substances:
Year: 2021 PMID: 34301844 PMCID: PMC8323969 DOI: 10.4049/jimmunol.2100059
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.426