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白细胞介素-1β通过核因子κB、丝裂原活化蛋白激酶和骨形态发生蛋白/信号转导和转录激活因子信号通路之间的相互作用对牙周膜干细胞成骨作用的双刃剑效应

Double-edged-sword effect of IL-1β on the osteogenesis of periodontal ligament stem cells via crosstalk between the NF-κB, MAPK and BMP/Smad signaling pathways.

作者信息

Mao C-Y, Wang Y-G, Zhang X, Zheng X-Y, Tang T-T, Lu E-Y

机构信息

Department of Prosthodontics, Shanghai Key Laboratory of Stomatology, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, 639 Zhizaoju Road, Shanghai, China.

Shanghai Key Laboratory of Orthopaedic Implant, Department of Orthopaedics Surgery, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, 639 Zhizaoju Road, Shanghai, China.

出版信息

Cell Death Dis. 2016 Jul 14;7(7):e2296. doi: 10.1038/cddis.2016.204.

Abstract

Microenvironmental conditions can interfere with the functional role and differentiation of mesenchymal stem cells (MSCs). Recent studies suggest that an inflammatory microenvironment can significantly impact the osteogenic potential of periodontal ligament stem cells (PDLSCs), but the precise effects and mechanisms involved remain unclear. Here, we show for the first time that interleukin-1β (IL-1β) has dual roles in the osteogenesis of PDLSCs at concentrations ranging from physiologically healthy levels to those found in chronic periodontitis. Low doses of IL-1β activate the BMP/Smad signaling pathway to promote the osteogenesis of PDLSCs, but higher doses of IL-1β inhibit BMP/Smad signaling through the activation of nuclear factor-κB (NF-κB) and mitogen-activated protein kinase (MAPK) signaling, inhibiting osteogenesis. These results demonstrate that crosstalk between NF-κB, MAPK and BMP/Smad signaling mediates this dual effect of IL-1β on PDLSCs. We also show that the impaired osteogenesis of PDLSCs results in more inflammatory cytokines and chemokines being released, inducing the chemotaxis of macrophages, which further clarifies the role of PDLSCs in the pathogenesis of periodontitis.

摘要

微环境条件可干扰间充质干细胞(MSCs)的功能作用和分化。最近的研究表明,炎症微环境可显著影响牙周膜干细胞(PDLSCs)的成骨潜能,但具体影响及相关机制仍不清楚。在此,我们首次表明,白细胞介素-1β(IL-1β)在生理健康水平至慢性牙周炎水平的浓度范围内,对PDLSCs的成骨具有双重作用。低剂量的IL-1β激活骨形态发生蛋白/ Smad信号通路,促进PDLSCs的成骨,但高剂量的IL-1β通过激活核因子-κB(NF-κB)和丝裂原活化蛋白激酶(MAPK)信号通路抑制骨形态发生蛋白/ Smad信号,从而抑制成骨。这些结果表明,NF-κB、MAPK和骨形态发生蛋白/ Smad信号之间的相互作用介导了IL-1β对PDLSCs的这种双重作用。我们还表明,PDLSCs成骨受损导致更多炎症细胞因子和趋化因子释放,诱导巨噬细胞趋化,这进一步阐明了PDLSCs在牙周炎发病机制中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f51/4973347/3e229408c50a/cddis2016204f1.jpg

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