Kimura T
Second Department of Pathology, Hokkaido University School of Medicine, Sapporo, Japan.
Hokkaido Igaku Zasshi. 1994 Jul;69(4):857-65.
The binding and entry of Japanese encephalitis virus (JEV) to established cell lines were analyzed using radiolabeled virion. A JEV high-susceptibility cell line, Vero cells, adsorbed and internalized much more JEV than did NRK cells, which is a low-susceptibility cell line. NRK cells injected with viral genomic RNA produced infectious virions in culture medium. Protease treatment of cells reduced the binding of JEV to Vero cells stronger than that to NRK cells. JEV bound to a 74 KD molecule present in membrane fraction of Vero cells and this binding was inhibited by a hemagglutinin-inhibiting monoclonal antibody against JEV (MAb 301). MAb 301 also inhibited the binding of JEV to Vero cells much more strongly than to the NRK cells. The 74 KD molecule was not detected in the membrane fraction of NRK cells. These results suggest that the process of binding and entry of JEV determine the JEV susceptibility of cells at least to a certain extent, and in particular suggest that the 74 KD molecule may be a possible candidate or component of the cellular receptor for JEV.
使用放射性标记的病毒粒子分析了日本脑炎病毒(JEV)与已建立的细胞系的结合及进入情况。一种JEV高敏感性细胞系——Vero细胞,吸附和内化的JEV比低敏感性细胞系NRK细胞多得多。注射了病毒基因组RNA的NRK细胞在培养基中产生了有感染性的病毒粒子。用蛋白酶处理细胞后,JEV与Vero细胞的结合减少程度比与NRK细胞的结合减少程度更强。JEV与Vero细胞膜组分中存在的一个74 KD分子结合,且这种结合被一种针对JEV的血凝抑制单克隆抗体(单克隆抗体301)所抑制。单克隆抗体301抑制JEV与Vero细胞结合的能力也比抑制其与NRK细胞结合的能力强得多。在NRK细胞膜组分中未检测到74 KD分子。这些结果表明,JEV的结合和进入过程至少在一定程度上决定了细胞对JEV的敏感性,尤其表明74 KD分子可能是JEV细胞受体的一个可能候选物或组成部分。