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DJ-1 promotes angiogenesis and osteogenesis by activating FGF receptor-1 signaling

机译:DJ-1通过激活FGF受体1信号传导促进血管生成和成骨

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摘要

Communication between osteoblasts and endothelial cells is essential for bone fracture repair, but the molecular identities of such communicating factors are not well defined. Here we identify DJ-1 as a novel mediator of the cross-talk between osteoblasts and endothelial cells through an unbiased screening of molecules secreted from human mesenchymal stem cells during osteogenesis. We show that DJ-1 stimulates the differentiation of human mesenchymal stem cells to osteoblasts and that DJ-1 induces angiogenesis in endothelial cells through activation of fibroblast growth factor receptor-1 signalling. In a rodent model of bone fracture repair, extracellular application of DJ-1 enhances bone regeneration in vivo by stimulating the formation of blood vessels and new bones. Both these effects are blocked by antagonizing fibroblast growth factor receptor-1 signalling. These findings uncover previously undefined extracellular roles of DJ-1 to promote angiogenesis and osteogenesis, suggesting DJ-1 may have therapeutic potential to stimulate bone regeneration.
机译:成骨细胞与内皮细胞之间的通讯对于骨折修复至关重要,但是这种通讯因素的分子特性尚不明确。在这里,我们通过在成骨过程中从人间充质干细胞分泌的分子的无偏筛选中,将DJ-1鉴定为成骨细胞与内皮细胞之间串扰的新型介体。我们显示DJ-1刺激人类间充质干细胞向成骨细胞分化,并且DJ-1通过激活成纤维细胞生长因子受体1信号传导诱导内皮细胞中的血管生成。在骨折修复的啮齿动物模型中,DJ-1的细胞外应用可通过刺激血管和新骨骼的形成来增强体内骨骼的再生。拮抗成纤维细胞生长因子受体1信号传导可阻断这两种作用。这些发现揭示了DJ-1在促进血管生成和成骨方面未曾定义的细胞外作用,表明DJ-1可能具有刺激骨再生的治疗潜力。

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