Halin Cornelia, Detmar Michael
Institute of Pharmaceutical Sciences, Swiss Federal Institute of Technology, ETH Zurich, Zurich, Switzerland.
Methods Enzymol. 2008;445:1-25. doi: 10.1016/S0076-6879(08)03001-2.
The growth of blood and lymphatic vessels, namely angiogenesis and lymphangiogenesis, is well known to be of importance for tumor growth and metastatic spread. In fact, several therapeutic strategies are currently being pursued in the clinic to interfere with these processes. By contrast, vascular remodeling associated with chronic inflammatory disorders, such as psoriasis, rheumatoid arthritis or inflammatory bowel disease, is only now emerging as a potential new target to treat these conditions. Animal models of inflammation, which mimic the inflammatory and the vascular phenotype of the disease, are important tools for studying inflammation and the accompanying (lymph)angiogenic response in vivo. This review provides a brief summary of our current knowledge of inflammation-induced angiogenesis and lymphangiogenesis and of selected mouse models that can be used to analyze these processes in vivo. It also provides a detailed description of methods, such as immunofluorescence or fluorescence-activated cell sorting (FACS) that can be used to visualize and quantitate vascular remodeling in inflamed tissues.
血管生成和淋巴管生成,即血液和淋巴管的生长,对于肿瘤生长和转移扩散的重要性已广为人知。事实上,目前临床上正在探索多种治疗策略来干预这些过程。相比之下,与慢性炎症性疾病(如银屑病、类风湿性关节炎或炎症性肠病)相关的血管重塑,直到现在才作为治疗这些疾病的潜在新靶点而出现。模拟疾病炎症和血管表型的炎症动物模型,是在体内研究炎症及伴随的(淋巴)血管生成反应的重要工具。本综述简要总结了我们目前对炎症诱导的血管生成和淋巴管生成的认识,以及可用于在体内分析这些过程的选定小鼠模型。它还详细描述了可用于可视化和定量炎症组织中血管重塑的方法,如免疫荧光或荧光激活细胞分选(FACS)。