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首页> 外文期刊>The Journal of biological chemistry >Activated Platelets Interfere with Recruitment of Mesenchymal Stem Cells to Apoptotic Cardiac Cells via High Mobility Group Box 1/Toll-like Receptor 4-mediated Down-regulation of Hepatocyte Growth Factor Receptor MET
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Activated Platelets Interfere with Recruitment of Mesenchymal Stem Cells to Apoptotic Cardiac Cells via High Mobility Group Box 1/Toll-like Receptor 4-mediated Down-regulation of Hepatocyte Growth Factor Receptor MET

机译:活化血小板干扰间充质干细胞的募集到凋亡心脏细胞通过高迁移率组箱1 /造成的受体4介导的肝细胞生长因子受体的下调

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Recruitment of mesenchymal stem cells (MSC) following cardiac injury, such as myocardial infarction, plays a critical role in tissue repair and may contribute to myocardial recovery. However, the mechanisms that regulate migration of MSC to the site of tissue damage remain elusive. Here, we demonstrate in vitro that activated platelets substantially inhibit recruitment of MSC toward apoptotic cardiac myocytes and fibroblasts. The alarmin high mobility group box 1 (HMGB1) was released by platelets upon activation and mediated inhibition of the cell death-dependent migratory response through Toll-like receptor (TLR)-4 expressed on the MSC. Migration of MSC to apoptotic cardiac myocytes and fibroblasts was driven by hepatocyte growth factor (HGF), and platelet activation was followed by HMGB1/TLR-4-dependent down-regulation of HGF receptor MET on MSC, thereby impairing HGF-driven MSC recruitment. We identify a novel mechanism by which platelets, upon activation, interfere with MSC recruitment to apoptotic cardiac cells, a process that may be of particular relevance for myocardial repair and regeneration.
机译:心脏损伤如心肌损伤后的间充质干细胞(MSC)在组织修复中发挥着关键作用,可能有助于心肌恢复。然而,调节MSC迁移到组织损伤部位的机制仍然难以捉摸。在这里,我们在体外证明活化血小板基本上抑制MSC的募集朝凋亡心肌细胞和成纤维细胞。通过在MSC上表达的Toll样受体(TLR)-4激活并介导细胞死亡依赖性迁移响应,通过血小板通过血小板释放出来的警报高迁移率组盒1(HMGB1)。 MSC的迁移到凋亡心肌细胞和成纤维细胞的迁移由肝细胞生长因子(HGF)驱动,然后在MSC上遇到HGF受体的HMGB1 / TLR-4依赖性下调,从而损害HGF驱动的MSC募集。我们鉴定了一种新的机制,在激活时血小板干扰MSC募集到凋亡心脏细胞,这是对心肌修复和再生的特定相关性的过程。

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