LOCALIZATION OF A TOXOPLASMA-GONDII RHOPTRY PROTEIN BY IMMUNOELECTRON MICROSCOPY DURING AND AFTER HOST-CELL PENETRATION

被引:101
|
作者
SAFFER, LD
MERCEREAUPUIJALON, O
DUBREMETZ, JF
SCHWARTZMAN, JD
机构
[1] UNIV VIRGINIA,SCH MED,DEPT PATHOL,CHARLOTTESVILLE,VA 22908
[2] INST PASTEUR,UNITE PARASITOL EXPTL,F-75724 PARIS 15,FRANCE
[3] INSERM,U42,F-59650 VILLENEUVE DASCQ,FRANCE
来源
JOURNAL OF PROTOZOOLOGY | 1992年 / 39卷 / 04期
关键词
CULTURED CELLS; ELECTRON MICROSCOPY; HUMAN FIBROBLASTS; IMMUNE SERUM; IMMUNOBLOT; IMMUNOLOCALIZATION TECHNIQUES; MONOCLONAL ANTIBODY; TG180 SARCOMA CELLS;
D O I
10.1111/j.1550-7408.1992.tb04844.x
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
We immunolocalized a Toxoplasma gondii rhoptry protein (ROP1) before and after parasite host cell invasion of human fibroblasts and TG180 murine sarcoma cells by electron microscopy and immunogold labeling using either a monoclonal antibody (Tg49) or a monospecific rabbit antiserum (alpha-249). At all stages of parasite growth ROP1 was found within the body but rarely within the peduncle of rhoptries, even in those that appeared empty. Immediately after host cell invasion ROP1 was associated with the parasitophorous vacuole membrane. Within hours after invasion the amount of ROP1 immunodetectable on the parasitophorous vacuole membrane was markedly decreased. The localization of ROP1 suggests a role in the early establishment of infection in host cells, consistent with previous work that has indicated that monoclonal antibodies to ROP1 (including the one used in these studies) interfere with the phenomenon of penetration enhancement.
引用
收藏
页码:526 / 530
页数:5
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