Sakurada S, Kato T, Mashiba K, Mori S, Okamoto T
Department of Molecular Genetics, Nagoya City University Medical School, Mizuho-ku.
Jpn J Cancer Res. 1996 Nov;87(11):1143-52. doi: 10.1111/j.1349-7006.1996.tb03124.x.
To examine the role of vascular endothelial growth factor (VEGF) in the development of edema associated with Kaposi's sarcoma (KS) in acquired immunodeficiency syndrome (AIDS), we exploited animal model systems to detect the activity that induces vascular hyper-permeability (VHP) using cultured AIDS-KS spindle cells. Cultured AIDS-KS spindle cells and conditioned medium (AIDS-KS-CM) that had been semi-purified through a heparin affinity column were tested for the ability to induce VHP in animals. The AIDS-KS spindle cells and AIDS-KS-CM induced VHP that was histamine-independent. The VHP-inducing activity was detected in the 0.5 M NaCl fraction from the heparin affinity column and was blocked by anti-VEGF neutralizing antibody. In addition, the production of VEGF was demonstrated in fresh AIDS-KS tissue as well as in cultured AIDS-KS cells, while control cells were negative for VEGF production. From these observations, we concluded that AIDS-KS cells produce a factor(s) that promotes VHP, and this factor could be VEGF.
为研究血管内皮生长因子(VEGF)在获得性免疫缺陷综合征(AIDS)相关的卡波西肉瘤(KS)水肿形成中的作用,我们利用动物模型系统,通过培养的AIDS-KS梭形细胞检测诱导血管高通透性(VHP)的活性。检测培养的AIDS-KS梭形细胞和经肝素亲和柱半纯化的条件培养基(AIDS-KS-CM)在动物体内诱导VHP的能力。AIDS-KS梭形细胞和AIDS-KS-CM诱导的VHP与组胺无关。在肝素亲和柱的0.5M NaCl组分中检测到VHP诱导活性,且该活性被抗VEGF中和抗体阻断。此外,新鲜AIDS-KS组织以及培养的AIDS-KS细胞中均证实有VEGF产生,而对照细胞VEGF产生呈阴性。基于这些观察结果,我们得出结论,AIDS-KS细胞产生促进VHP的一种或多种因子,且该因子可能是VEGF。