Prudhomme J G, Sherman I W, Land K M, Moses A V, Stenglein S, Nelson J A
Department of Biology, University of California, Riverside 92521, USA.
Int J Parasitol. 1996 Jun;26(6):647-55. doi: 10.1016/0020-7519(96)00027-6.
The cytoadherence of Plasmodium falciparum-infected erythrocytes was studied using immortalized human brain capillary endothelial cells. The immortalized cells, denoted as BB19, derived from the human brain endothelium, were transformed with the E6E7 genes of human papilloma virus and retained their endothelial nature, i.e. tubule formation occurred with Matrigel as a substratum and the cells stained positive for Factor VIII-related antigen, or vonWillebrand's factor. Surface expression of ICAM-1, VCAM, E-selectin, and CD36 was demonstrated by immunofluorescence staining with monoclonal antibodies to these ligands. Exposure to cytokines (TNF, IFN gamma, IL-1 alpha, and IL-6) and lipopolysaccharide resulted in an increase in expression of ICAM-1, VCAM, E-selectin, and CD36. The BB19 cells bound P. falciparum-infected red blood cells with both the FCR-3 and the ITO4 strains. Antibodies to CD36 and ICAM-1 partially inhibited the binding of the FCR-3 and the ITO4 lines, respectively. These findings suggest that BB19 cells may be useful in the analysis of receptor-based cytoadherence and sequestration, as well as in the cell biology of microvessel formation.
利用永生化人脑微血管内皮细胞研究了恶性疟原虫感染红细胞的细胞黏附情况。这些永生化细胞被命名为BB19,源自人脑内皮细胞,用人乳头瘤病毒的E6E7基因进行了转化,并保留了其内皮细胞特性,即使用基质胶作为底物时可形成小管,且细胞对VIII因子相关抗原或血管性血友病因子呈阳性染色。通过用针对这些配体的单克隆抗体进行免疫荧光染色,证实了细胞间黏附分子-1(ICAM-1)、血管细胞黏附分子(VCAM)、E-选择素和CD36的表面表达。暴露于细胞因子(肿瘤坏死因子、干扰素γ、白细胞介素-1α和白细胞介素-6)和脂多糖会导致ICAM-1、VCAM、E-选择素和CD36的表达增加。BB19细胞能与FCR-3和ITO4菌株感染的恶性疟原虫红细胞结合。针对CD36和ICAM-1的抗体分别部分抑制了FCR-3和ITO4细胞系的结合。这些发现表明,BB19细胞可能有助于基于受体的细胞黏附和滞留分析,以及微血管形成的细胞生物学研究。