Many intracellular parasites are capable of penetrating host epithelial barriers. To study this process in more detail we examined the interactions between the pathogenic bacteria Salmonella choleraesuis and polarized epithelial monolayers of Madin-Darby canine kidney (MDCK) cells grown on membrane filters. Association of bacteria with the MDCK cell apical surface was an active event, requiring bacterial RNA and protein synthesis, and was blocked by low temperatures. Salmonella were internalized within a membrane-bound vacuole and exhibited penetration through, but not between MDCK cells. A maximum of 14 Salmonella per MDCK cell crossed the monolayer per hour to the basolateral surface yet the monolayer remained viable and impermeable to Escherichia coli. Apical S. choleraesuis infection resulted in an increase in paracellular permeability but the MDCK intercellular contacts were not significantly disrupted. Basolateral S. choleraesuis infection was inefficient, and only small numbers of S. choleraesuis penetrated to the apical medium.
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1 July 1988
Article|
July 01 1988
Penetration of Salmonella through a polarized Madin-Darby canine kidney epithelial cell monolayer.
B B Finlay,
B B Finlay
Department of Medical Microbiology, Stanford University School of Medicine, California 94305.
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B Gumbiner,
B Gumbiner
Department of Medical Microbiology, Stanford University School of Medicine, California 94305.
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S Falkow
S Falkow
Department of Medical Microbiology, Stanford University School of Medicine, California 94305.
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B B Finlay
Department of Medical Microbiology, Stanford University School of Medicine, California 94305.
B Gumbiner
Department of Medical Microbiology, Stanford University School of Medicine, California 94305.
S Falkow
Department of Medical Microbiology, Stanford University School of Medicine, California 94305.
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1988) 107 (1): 221–230.
Citation
B B Finlay, B Gumbiner, S Falkow; Penetration of Salmonella through a polarized Madin-Darby canine kidney epithelial cell monolayer.. J Cell Biol 1 July 1988; 107 (1): 221–230. doi: https://doi.org/10.1083/jcb.107.1.221
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