Echovirus 1 Entry into Polarized Caco-2 Cells Depends on Dynamin, Cholesterol, and Cellular Factors Associated with Macropinocytosis

被引:43
|
作者
Krieger, Sophie E. [1 ]
Kim, Chonsaeng [1 ]
Zhang, Lili [1 ]
Marjomaki, Varpu [2 ]
Bergelson, Jeffrey M. [1 ,3 ]
机构
[1] Childrens Hosp Philadelphia, Div Infect Dis, Philadelphia, PA 19104 USA
[2] Univ Jyvaskyla, Dept Biol & Environm Sci, Nanosci Ctr, Jyvaskyla, Finland
[3] Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA
基金
芬兰科学院;
关键词
EPITHELIAL TIGHT JUNCTIONS; STOMATITIS-VIRUS ENTRY; COXSACKIEVIRUS ENTRY; MEDIATED ENDOCYTOSIS; INTEGRIN VLA-2; RECEPTOR; REQUIRES; INTERNALIZATION; INHIBITION; CAVEOSOMES;
D O I
10.1128/JVI.03415-12
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Enteroviruses invade their hosts by crossing the intestinal epithelium. We have examined the mechanism by which echovirus 1 (EV1) enters polarized intestinal epithelial cells (Caco-2). Virus binds to VLA-2 on the apical cell surface and moves rapidly to early endosomes. Using inhibitory drugs, dominant negative mutants, and small interfering RNAs (siRNAs) to block specific endocytic pathways, we found that virus entry requires dynamin GTPase and membrane cholesterol but is independent of both clathrin- and caveolin-mediated endocytosis. Instead, infection requires factors commonly associated with macropinocytosis, including amiloride-sensitive Na+/H+ exchange, protein kinase C, and C-terminal-binding protein-1 (CtBP1); furthermore, EV1 accumulates rapidly in intracellular vesicles with dextran, a fluid-phase marker. These results suggest a role for macropinocytosis in the process by which EV1 enters polarized cells to initiate infection.
引用
收藏
页码:8884 / 8895
页数:12
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