Hudon V, Berthod F, Black A F, Damour O, Germain L, Auger F A
Laboratoire d'Organogenèse Expérimentale, Département de Chirurgie, Université Laval, CHA, Hôpital du Saint-Sacrement, 1050 Chemin Sainte-Foy, Québec, Canada, G1S 4L8.
Br J Dermatol. 2003 Jun;148(6):1094-104. doi: 10.1046/j.1365-2133.2003.05298.x.
Because angiogenesis is a major feature of different physiological and pathological situations, the identification of factors that stimulate or inhibit this process and the elucidation of their mechanisms of action are most certainly of clinical relevance. We have produced a new model of endothelialized reconstructed dermis that promotes the spontaneous formation of a human capillary-like network and its stabilization in vitro for a period longer than 1 month.
The aim of this work was to describe the three-dimensional structure of the capillary-like network. Thereafter we strove to study, quantitatively and qualitatively, the influence of angiogenic and angiostatic drugs on capillary-like tube (CLT) formation in vitro in the model.
The endothelialized dermis was prepared by coculturing two human cell types, dermal fibroblasts and umbilical vein endothelial cells, in a collagen sponge biomaterial.
The visualization by confocal microscopy of the tubes present in the model showed that the endothelial structures were not cord-like but rather CLTs with well-defined lumina. Moreover, these tubes were organized in a complex network of branching structures. When angiogenic factors (vascular endothelial growth factor 10 ng mL-1 or basic fibroblast growth factor 10 ng mL-1) were added to the model, 1.8 and 1.4 times more capillaries, respectively, were observed, whereas the addition of progesterone (10 microg x mL(-1)) reduced by 2.4 times the number of tubes compared with the control.
These results suggest that this model is a highly efficient assay for the screening of potentially angiogenic and angiostatic compounds.
由于血管生成是不同生理和病理状况的主要特征,因此鉴定刺激或抑制该过程的因素并阐明其作用机制无疑具有临床意义。我们构建了一种新的内皮化重建真皮模型,该模型可促进人毛细血管样网络的自发形成,并使其在体外稳定长达1个月以上。
这项工作的目的是描述毛细血管样网络的三维结构。此后,我们致力于定量和定性地研究血管生成和血管生成抑制药物对该模型中体外毛细血管样管(CLT)形成的影响。
通过在胶原海绵生物材料中共培养两种人类细胞类型,即真皮成纤维细胞和脐静脉内皮细胞,制备内皮化真皮。
共聚焦显微镜观察模型中的管显示,内皮结构不是索状,而是具有明确管腔的CLT。此外,这些管组织成复杂的分支结构网络。当向模型中添加血管生成因子(血管内皮生长因子10 ng/mL或碱性成纤维细胞生长因子10 ng/mL)时,分别观察到毛细血管数量增加1.8倍和1.4倍,而添加孕酮(10 μg/mL)使管的数量比对照减少2.4倍。
这些结果表明,该模型是筛选潜在血管生成和血管生成抑制化合物的高效检测方法。