EFFECTS OF PROTEIN-KINASE-C INHIBITORS ON VIRAL ENTRY AND INFECTIVITY

被引:54
作者
CONSTANTINESCU, SN
CERNESCU, CD
POPESCU, LM
机构
[1] FAC MED BUCHAREST,DIV CELL BIOL,POB 35-10,R-35 BUCHAREST,ROMANIA
[2] NICOLAU INST VIROL,BUCHAREST,ROMANIA
关键词
PROTEIN KINASE-C; VIRAL ENTRY; VIRAL INFECTIVITY; ENVELOPED VIRUS; ENDOCYTOSIS;
D O I
10.1016/0014-5793(91)80826-O
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The protein kinase C inhibitor H-7 (2-20-mu-M) inhibited dose-dependently the infectivity of the vesicular stomatitis virus on cultured human fibroblasts. Electron microscopy showed that H-7 inhibited the viral entry. H-7 also inhibited the infectivity of four other enveloped viruses, herpes simplex I, turkey herpes, vaccinia and Sindbis. Similar results were obtained using staurosporine (2.5 nM), tamoxifen (40-mu-M), phloretin (140-mu-M), or W-7 (40-mu-M). However, the infectivity of non-enveloped viruses (e.g. poliomyelitis I) was not inhibited by H-7. These results show that protein kinase C is critically involved in the infectivity of enveloped viruses, most probably at the level of viral entry (receptor-mediated endocytosis).
引用
收藏
页码:31 / 33
页数:3
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