Sunderkötter C, Roth J, Sorg C
Institute of Experimental Dermatology, University of Münster, Federal Republic of Germany.
Am J Pathol. 1990 Sep;137(3):511-5.
Tumor necrosis factor alpha (TNF-alpha) and basic fibroblast growth factor (bFGF) have been assigned a major role in the induction of angiogenesis. By performing immunohistochemical studies of cauterized mouse corneas, the in situ distribution of bFGF and TNF-alpha in the course of inflammatory neovascularization was investigated. bFGF was found throughout the corneal epithelium of untreated and cauterized eyes. However it was only rarely detected in the endothelium or in infiltrating cells before the onset of neovascularization. TNF-alpha was not expressed by any cell before the ingrowth of new blood vessels, which took place within 36 hours after cauterization. It is concluded that the release of these cytokines by infiltrating cells is of minor or no importance for the induction of sterile inflammatory angiogenesis.
肿瘤坏死因子α(TNF-α)和碱性成纤维细胞生长因子(bFGF)在血管生成诱导过程中被认为起着主要作用。通过对烧灼后的小鼠角膜进行免疫组织化学研究,调查了bFGF和TNF-α在炎症性新生血管形成过程中的原位分布。在未处理和烧灼后的眼睛的整个角膜上皮中均发现了bFGF。然而,在新生血管形成开始之前,在内皮细胞或浸润细胞中很少检测到bFGF。在烧灼后36小时内出现新生血管长入之前,任何细胞均未表达TNF-α。结论是,浸润细胞释放这些细胞因子对于无菌性炎症性血管生成的诱导作用较小或无重要意义。