Regulation of sclerostin by the SIRT1 stabilization pathway in osteocytes

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Osteocytes play a critical role in bone remodeling through the secretion of paracrine factors regulating the differentiation and activity of osteoblasts and osteoclasts. Sclerostin is a key osteocyte-derived factor that suppresses bone formation and promotes bone resorption, therefore regulators of sclerostin secretion are a likely source of new therapeutic strategies for treatment of skeletal disorders. Here, we demonstrate that protein kinase CK2 (casein kinase 2) controls sclerostin expression in osteocytes via the deubiquitinase ubiquitin-specific peptidase 4 (USP4)-mediated stabilization of Sirtuin1 (SIRT1). Deletion of CK2 regulatory subunit, Csnk2b, in osteocytes (Csnk2b(Dmp1)) results in low bone mass due to elevated levels of sclerostin. This phenotype in Csnk2b(Dmp1) mice was partly reversed when sclerostin expression was downregulated by a single intravenous injection with bone-targeting adeno-associated virus 9 (AAV9) carrying an artificial-microRNA that targets Sost. Mechanistically, CK2-induced phosphorylation of USP4 is important for stabilization of SIRT1 by suppressing ubiquitin-dependent proteasomal degradation. Upregulated expression of SIRT1 inhibits sclerostin transcription in osteocytes. Collectively, the CK2-USP4-SIRT1 pathway is crucial for the regulation of sclerostin expression in osteocytes to maintain bone homeostasis.
Publisher
SPRINGERNATURE
Issue Date
2022-02
Language
English
Article Type
Article
Citation

CELL DEATH AND DIFFERENTIATION, v.29, no.8, pp.1625 - 1638

ISSN
1350-9047
DOI
10.1038/s41418-022-00952-x
URI
http://hdl.handle.net/10203/297914
Appears in Collection
MA-Journal Papers(저널논문)
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