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Macrophage-Specific Expression of Urokinase-Type Plasminogen Activator Promotes Skeletal Muscle Regeneration

机译:尿激酶型纤溶酶原激活物的巨噬细胞特异性表达促进骨骼肌再生。

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Macrophages (Mp) and the plasminogen system play important roles in tissue repair following injury. We hypothesized that Mp-specific expression of urokinase-type plasminogen activator (uPA) is sufficient for Mp to migrate into damaged muscle and for efficient muscle regeneration. We generated transgenic mice expressing uPA only in Mp, and we assessed the ability of these mice to repair muscle injury. Mp-only uPA expression was sufficient to induce wild-type levels of Mp accumulation, angiogenesis, and new muscle fiber formation. In mice with wild-type uPA expression, Mp-specific overexpression further increased Mp accumulation and enhanced muscle fiber regeneration. Furthermore, Mp expression of uPA regulated the level of active hepatocyte growth factor, which is required for muscle fiber regeneration, in damaged muscle. In vitro studies demonstrated that uPA promotes Mp migration through proteolytic and nonproteolytic mechanisms, including proteolytic activation of hepatocyte growth factor. In summary, Mp-derived uPA promotes muscle regeneration by inducing Mp migration, angiogenesis, and myogenesis.
机译:巨噬细胞(Mp)和纤溶酶原系统在损伤后的组织修复中起重要作用。我们假设尿激酶型纤溶酶原激活物(uPA)的Mp特异性表达足以使Mp迁移到受损的肌肉中并有效地进行肌肉再生。我们生成了仅在Mp中表达uPA的转基因小鼠,并且我们评估了这些小鼠修复肌肉损伤的能力。仅Mp的uPA表达足以诱导野生型水平的Mp积累,血管生成和新的肌纤维形成。在具有野生型uPA表达的小鼠中,Mp特异性过度表达进一步增加了Mp积累并增强了肌纤维再生。此外,uPA的Mp表达调节受损肌肉中肌肉纤维再生所需的活性肝细胞生长因子的水平。体外研究表明,uPA通过蛋白水解和非蛋白水解机制(包括肝细胞生长因子的蛋白水解激活)促进Mp迁移。总之,Mp衍生的uPA通过诱导Mp迁移,血管生成和肌生成来促进肌肉再生。

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