Key result
Echovirus 1 entry into polarized Caco-2 cells requires dynamin GTPase, membrane cholesterol, and macropinocytosis-associated factors, but is independent of clathrin- and caveolin-mediated endocytosis.
Echovirus 1 enters polarized intestinal epithelial cells via a macropinocytosis-like pathway dependent on dynamin and cholesterol, rather than clathrin or caveolin.
Hypothesis-generating for entry inhibitors in enteroviral disease; leaves open translation from polarized cell models to patients.
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.
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Krieger et al. (2013) studied Echovirus 1 infection. Inhibitory drugs, dominant negative mutants, and siRNAs was evaluated on Mechanism of echovirus 1 entry into polarized intestinal epithelial cells. Echovirus 1 entry into polarized Caco-2 cells requires dynamin GTPase, membrane cholesterol, and macropinocytosis-associated factors, but is independent of clathrin- and caveolin-mediated endocytosis.
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