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尿激酶型纤溶酶原激活物在巨噬细胞中的特异性表达促进骨骼肌再生。

Macrophage-specific expression of urokinase-type plasminogen activator promotes skeletal muscle regeneration.

机构信息

Department of Kinesiology and Nutrition, University of Illinois, Chicago, IL 60612, USA.

出版信息

J Immunol. 2011 Aug 1;187(3):1448-57. doi: 10.4049/jimmunol.1004091. Epub 2011 Jun 27.

Abstract

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.

摘要

巨噬细胞 (Mp) 和纤溶酶原系统在损伤后组织修复中发挥重要作用。我们假设 Mp 特异性表达尿激酶型纤溶酶原激活物 (uPA) 足以使 Mp 迁移到受损肌肉中,并实现有效的肌肉再生。我们生成了仅在 Mp 中表达 uPA 的转基因小鼠,并评估了这些小鼠修复肌肉损伤的能力。Mp 中仅表达 uPA 就足以诱导 Mp 积累、血管生成和新肌纤维形成达到野生型水平。在具有野生型 uPA 表达的小鼠中,Mp 特异性过表达进一步增加了 Mp 积累并增强了肌纤维再生。此外,uPA 在受损肌肉中调节活性肝细胞生长因子的水平,这是肌纤维再生所必需的。体外研究表明,uPA 通过蛋白水解和非蛋白水解机制促进 Mp 迁移,包括肝细胞生长因子的蛋白水解激活。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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