Casein kinase 2 beta as a novel enhancer of activin-like receptor-1 signaling

Article

关键词: GROWTH-FACTOR-BETA;    HEREDITARY HEMORRHAGIC TELANGIECTASIA;    ENDOTHELIAL-CELL MIGRATION;    SMAD1/5 PHOSPHORYLATION;    REGULATORY SUBUNIT;    INHIBITS MOS;    I RECEPTORS;    PROTEIN;    ENDOGLIN;    CK2;   

DOI  :  10.1096/fj.09-131607

来源: SCIE

【 摘 要 】

ALK-1 is a transforming growth factor beta (TGF-beta) superfamily receptor that is predominantly expressed in endothelial cells and is essential for angiogenesis, as demonstrated by the embryonic lethal phentoype when targeted for deletion in mice and its mutation in the human disease hereditary hemorrhagic telangiectasia. Although ALK-1 and the endothelial-specific TGF-beta superfamily coreceptor, endoglin, form a heteromeric complex and bind similar TGF-beta superfamily ligands, their signaling mechanisms remain poorly characterized. Here we report the identification of CK2 beta, the regulatory subunit of protein kinase CK2, as a novel enhancer of ALK-1 signaling. The cytoplasmic domain of ALK-1 specifically binds to CK2 beta in vitro and in vivo. NAAIRS mutagenesis studies define amino acid sequences 181-199 of CK2 beta and 207-212 of ALK-1 as the interaction domains, respectively. The ALK-1/CK2 beta interaction specifically enhanced Smad1/5/8 phosphorylation and ALK-1-mediated reporter activation in response to TGF-beta 1 and BMP-9 treatment. In a reciprocal manner, siRNA-mediated silencing of endogenous CK2 beta inhibited TGF-beta 1 and BMP-9-stimulated Smad1/5/8 phosphorylation and ALK-1-mediated reporter activation. Functionally, CK2 beta enhanced the ability of activated or ligand-stimulated ALK-1 to inhibit endothelial cell migration. Similarly, ALK-1 and CK2 beta antagonized endothelial tubule formation in Matrigel. These studies support CK2 beta as an important regulator of ALK-1 signaling and ALK-1-mediated functions in endothelial cells.-Lee, N. Y., Haney, J. C., Sogani, J., Blobe, G. C. Casein kinase 2 beta as a novel enhancer of activin-like receptor-1 signaling. FASEB J. 23, 3712-3721 (2009). www.fasebj.org

【 授权许可】

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