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Sprouty 2,机械加载和成骨分化过程中FosB和间充质干细胞增殖的早期反应基因调节因子。

Sprouty 2, an Early Response Gene Regulator of FosB and Mesenchymal Stem Cell Proliferation During Mechanical Loading and Osteogenic Differentiation.

作者信息

Schneider A Kristin, Cama Giuseppe, Ghuman Mandeep, Hughes Francis J, Gharibi Borzo

机构信息

Division of Tissue Engineering and Biophotonics, Dental Institute, King's College London, Tower Wing, Guy's Hospital, London, SE1 9RT, UK.

出版信息

J Cell Biochem. 2017 Sep;118(9):2606-2614. doi: 10.1002/jcb.26035. Epub 2017 May 23.

DOI:10.1002/jcb.26035
PMID:28387432
Abstract

Sprouty 2 (Spry2), an inhibitor of MAP kinase signaling was previously shown by our group to be induced during mechanical loading of mesenchymal stem cells (MSCs). Here, we studied the implication of Spry2 activation during mechanical loading and chemically induced MSC differentiation. Spry 2 expression showed an immediate early response during mechanical loading and chemical induction of osteogenic differentiation and followed the same pattern as osteogenic associated gene FosB and was necessary for the induction of FosB, as Spry 2 knock down also abrogated the upregulation of FosB expression. Spry 2 knock down was, also associated with an early response of the osteogenic genes Runx-2 and ALP. Neither the knock-down of Spry 2 nor the subsequent reduction in FosB had any effect on mid-late osteogenesis or mineralization but was associated with a significant increase in proliferation of MSC. These effects were possibly governed by negative regulation of MEK/Erk signaling as Spry 2 knock down resulted in an increase in phosphorylation of Erk1/2. In summary, our results shows the involvement of Spry2 in regulation of FosB and Runx2 genes, MAPK signaling and proliferation of MSC. Taken together these results suggest a possible role for Spry2 in regulation of MSC functions in response to mechanical loading and osteogenic differentiation. J. Cell. Biochem. 118: 2606-2614, 2017. © 2017 Wiley Periodicals, Inc.

摘要

Sprouty 2(Spry2)是一种丝裂原活化蛋白激酶信号通路的抑制剂,我们团队之前发现它在间充质干细胞(MSC)机械加载过程中被诱导表达。在此,我们研究了机械加载和化学诱导MSC分化过程中Spry2激活的意义。Spry2表达在机械加载和化学诱导成骨分化过程中呈现即时早期反应,并且与成骨相关基因FosB遵循相同模式,且对于FosB的诱导是必需的,因为敲低Spry2也消除了FosB表达的上调。敲低Spry2还与成骨基因Runx-2和碱性磷酸酶(ALP)的早期反应相关。敲低Spry2以及随后FosB的减少对中晚期成骨或矿化均无任何影响,但与MSC增殖的显著增加相关。这些效应可能受MEK/Erk信号通路的负调控,因为敲低Spry2导致Erk1/2磷酸化增加。总之,我们的结果表明Spry2参与FosB和Runx2基因的调控、MAPK信号通路以及MSC的增殖。综合这些结果表明,Spry2在响应机械加载和成骨分化调控MSC功能方面可能发挥作用。《细胞生物化学杂志》118: 2606 - 2614, 2017。© 2017威利期刊公司

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