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DUSP5 promotes osteogenic differentiation through SCP1/2‐dependent phosphorylation of SMAD1 by Xuejiao Liu; Xuenan Liu; Yangge Du; Menglong Hu; Yueming Tian; Zheng Li; Longwei Lv; Xiao Zhang; Yunsong Liu; Yongsheng Zhou; Ping Zhang is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

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## Abstract Dual‐specificity phosphatases (DUSPs) are defined by their capability to dephosphorylate both phosphoserine/phosphothreonine (pSer/pThr) and phosphotyrosine (pTyr). DUSP5, a member of DUSPs superfamily, is located in the nucleus and plays crucially regulatory roles in the signaling pathway transduction. In our present study, we discover that DUSP5 significantly promotes osteogenic differentiation of mesenchymal stromal cells (MSCs) by activating SMAD1 signaling pathway. Mechanistically, DUSP5 physically interacts with the phosphatase domain of small C‐terminal phosphatase 1/2 (SCP1/2, SMAD1 phosphatases) by the linker region. In addition, we further confirm that DUSP5 activates SMAD1 signaling through a SCP1/2‐dependent manner. Specifically, DUSP5 attenuates the SCP1/2‐SMAD1 interaction by competitively binding to SCP1/2, which is responsible for the SMAD1 dephosphorylation, and thus results in the activation of SMAD1 signaling. Importantly, DUSP5 expression in mouse bone marrow MSCs is significantly reduced in ovariectomized (OVX) mice in which osteogenesis is highly passive, and overexpression of __Dusp5__ via tail vein injection reverses the bone loss of OVX mice eff

Who reads DUSP5 promotes osteogenic differentiation through SCP1/2‐dependent phosphorylation of SMAD1?

Author

Xuejiao Liu; Xuenan Liu; Yangge Du; Menglong Hu; Yueming Tian; Zheng Li; Longwei Lv; Xiao Zhang; Yunsong Liu; Yongsheng Zhou; Ping Zhang

Publisher

Oxford University Press (OUP)

Published

2021

Language

EN

Field

Biochemistry, Genetics and Molecular Biology (Life Sciences)