Mahadevan V, Hart I R, Lewis G P
Department of Pharmacology, Royal College of Surgeons of England, London, United Kingdom.
Cancer Res. 1989 Jan 15;49(2):415-9.
A new quantitative assay for measuring angiogenesis in a s.c. located sponge implant in rats is described. Using this model, which detects neovascularization by measuring alterations in 133Xe clearance, it has been shown that the known angiogenic factors, transforming growth factor alpha and tumor necrosis factor alpha, cause maximum vascularization of the sponge to occur by Day 11 postimplantation compared with Days 15 to 17 in control animals. The monokine interleukin 1 alpha is shown to be strongly angiogenic, suggesting that more than one macrophage-derived cytokine may be the active mediator in macrophage-induced angiogenesis. Extracellular matrix proteins appear to play a role in regulating the angiogenic response such that presoaking sponges in laminin (40 micrograms/ml) or fibrinogen (500 micrograms/ml) solutions induced a significant reduction in the time taken to achieve maximum 133Xe clearance values; no such enhancement of neovascularization was observed when sponges were presoaked in type IV collagen (100 micrograms/ml) solution. The assay described here, which is reproducible, objective, and quantitative, should be of considerable use in elucidating the molecular basis of angiogenesis regulation.
本文描述了一种新的定量测定方法,用于测量大鼠皮下植入海绵中的血管生成情况。使用该模型,通过测量¹³³Xe清除率的变化来检测新血管形成,结果表明,已知的血管生成因子,即转化生长因子α和肿瘤坏死因子α,与对照动物在植入后第15至17天相比,在植入后第11天可使海绵的血管生成达到最大值。单核因子白细胞介素1α被证明具有强烈的血管生成作用,这表明可能不止一种巨噬细胞衍生的细胞因子是巨噬细胞诱导血管生成的活性介质。细胞外基质蛋白似乎在调节血管生成反应中起作用,例如将海绵预先浸泡在层粘连蛋白(40微克/毫升)或纤维蛋白原(500微克/毫升)溶液中,可显著缩短达到最大¹³³Xe清除率值所需的时间;而当海绵预先浸泡在IV型胶原(100微克/毫升)溶液中时,未观察到新血管生成的这种增强。本文所述的测定方法具有可重复性、客观性和定量性,在阐明血管生成调节的分子基础方面应具有相当大的用途。