首页> 美国卫生研究院文献>Stem Cells International >IL-1β-Induced Matrix Metalloprotease-1 Promotes Mesenchymal Stem Cell Migration via PAR1 and G-Protein-Coupled Signaling Pathway
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IL-1β-Induced Matrix Metalloprotease-1 Promotes Mesenchymal Stem Cell Migration via PAR1 and G-Protein-Coupled Signaling Pathway

机译:IL-1β诱导的基质金属蛋白酶1通过PAR1和G蛋白偶联的信号通路促进间充质干细胞迁移

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摘要

Mesenchymal stem cells (MSCs) are known for homing to sites of injury in response to signals of cellular damage. However, the mechanisms of how cytokines recruit stem cells to target tissue are still unclear. In this study, we found that the proinflammation cytokine interleukin-1β (IL-1β) promotes mesenchymal stem cell migration. The cDNA microarray data show that IL-1β induces matrix metalloproteinase-1 (MMP-1) expression. We then used quantitative real-time PCR and MMP-1 ELISA to verify the results. MMP-1 siRNA transfected MSCs, and MSC pretreatment with IL-1β inhibitor interleukin-1 receptor antagonist (IL-1RA), MMP tissue inhibitor of metalloproteinase 1 (TIMP1), tissue inhibitor of metalloproteinase 2 (TIMP2), MMP-1 inhibitor GM6001, and protease-activated receptor 1 (PAR1) inhibitor confirms that PAR1 protein signaling pathway leads to IL-1β-induced cell migration. In conclusion, IL-1β promotes the secretion of MMP-1, which then activates the PAR1 and G-protein-coupled signal pathways to promote mesenchymal stem cell migration.
机译:间充质干细胞(MSCs)响应细胞损伤信号而归巢到损伤部位。但是,细胞因子如何将干细胞募集到靶组织的机制仍不清楚。在这项研究中,我们发现促炎症细胞因子白介素-1β(IL-1β)促进间充质干细胞迁移。 cDNA微阵列数据显示IL-1β诱导基质金属蛋白酶1(MMP-1)表达。然后,我们使用定量实时PCR和MMP-1 ELISA验证结果。 MMP-1 siRNA转染的MSC,并用IL-1β抑制剂白介素1受体拮抗剂(IL-1RA),金属蛋白酶1的MMP组织抑制剂(TIMP1),金属蛋白酶2的组织抑制剂(TIMP2),MMP-1抑制剂GM6001进行MSC预处理,和蛋白酶激活受体1(PAR1)抑制剂证实PAR1蛋白信号通路导致IL-1β诱导的细胞迁移。总之,IL-1β促进MMP-1的分泌,然后激活PAR1和G蛋白偶联的信号通路,促进间充质干细胞迁移。

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