Literature DB >> 9199460

Epithelial cell polarity affects susceptibility to Pseudomonas aeruginosa invasion and cytotoxicity.

S M Fleiszig1, D J Evans, N Do, V Vallas, S Shin, K E Mostov.   

Abstract

Intact tissues are relatively resistant to Pseudomonas aeruginosa-induced disease, and injury predisposes tissue to infection. Intact epithelia contain polarized cells that have distinct apical and basolateral membranes with unique lipids and proteins. In this study, the role of cell polarity in epithelial cell susceptibility to P. aeruginosa virulence mechanisms was tested. Madin-Darby canine kidney (MDCK) cells, human corneal epithelial cells, and primary cultures of two different types of airway epithelial cells were grown on Transwell filters or in plastic tissue culture wells. P. aeruginosa invasion of cells was quantified by gentamicin survival assays with two isolates that invade epithelial cells (6294 and PAO1). Cytotoxic activity was assessed by trypan blue exclusion assays with two cytotoxic strains (6206 and PA103). Basolateral surfaces of cells were exposed by one of two methods: EGTA pretreatment of epithelial cells or growth of cells in low-calcium medium. Both methods of exposing basolateral membranes increased epithelial cell susceptibility to P. aeruginosa invasion and cytotoxicity. Migrating cells were also found to be more susceptible to P. aeruginosa invasion than confluent monolayers that had established membrane polarity. Monolayers of MDCK cells that had been selected for resistance to killing by concanavalin A were resistant to both cytotoxicity and invasion by P. aeruginosa because they were more efficiently polarized for their susceptibility to P. aeruginosa virulence factors than regular MDCK cells and not because they were defective in glycosylation. These results suggest that there are factors on the basolateral surfaces of epithelial cells that promote interaction with P. aeruginosa or that there are inhibitory factors on the apical cell surface. Thus, cell polarity of intact epithelia is likely to contribute to defense against P. aeruginosa infection.

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Year:  1997        PMID: 9199460      PMCID: PMC175402          DOI: 10.1128/iai.65.7.2861-2867.1997

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  34 in total

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Review 4.  Cell surface polarity in epithelia.

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5.  Tight junction formation in cultured epithelial cells (MDCK).

Authors:  L Gonzalez-Mariscal; B Chávez de Ramírez; M Cereijido
Journal:  J Membr Biol       Date:  1985       Impact factor: 1.843

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Authors:  H K Meiss; R F Green; E J Rodriguez-Boulan
Journal:  Mol Cell Biol       Date:  1982-10       Impact factor: 4.272

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Journal:  Cell       Date:  1984-08       Impact factor: 41.582

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Authors:  R L Boyd; R Ramphal; R Rice; J A Mangos
Journal:  Infect Immun       Date:  1983-03       Impact factor: 3.441

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Authors:  S Basak; R W Compans
Journal:  J Virol       Date:  1989-07       Impact factor: 5.103

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Authors:  A Martinez-Palomo; I Meza; G Beaty; M Cereijido
Journal:  J Cell Biol       Date:  1980-12       Impact factor: 10.539

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  79 in total

1.  Differential sensitivity of human epithelial cells to Pseudomonas aeruginosa exoenzyme S.

Authors:  E M McGuffie; J E Fraylick; D J Hazen-Martin; T S Vincent; J C Olson
Journal:  Infect Immun       Date:  1999-07       Impact factor: 3.441

2.  CFTR is a pattern recognition molecule that extracts Pseudomonas aeruginosa LPS from the outer membrane into epithelial cells and activates NF-kappa B translocation.

Authors:  Torsten H Schroeder; Martin M Lee; Patrick W Yacono; Carolyn L Cannon; A Alev Gerçeker; David E Golan; Gerald B Pier
Journal:  Proc Natl Acad Sci U S A       Date:  2002-05-07       Impact factor: 11.205

3.  Traversal of multilayered corneal epithelia by cytotoxic Pseudomonas aeruginosa requires the phospholipase domain of exoU.

Authors:  Julio C Ramirez; Suzanne M J Fleiszig; Aaron B Sullivan; Connie Tam; Roya Borazjani; David J Evans
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-01-25       Impact factor: 4.799

4.  Transcriptome analysis of Pseudomonas aeruginosa after interaction with human airway epithelial cells.

Authors:  Anders Frisk; Jill R Schurr; Guoshun Wang; Donna C Bertucci; Luis Marrero; Sung Hei Hwang; Daniel J Hassett; Michael J Schurr
Journal:  Infect Immun       Date:  2004-09       Impact factor: 3.441

Review 5.  Contact lens-related microbial keratitis: how have epidemiology and genetics helped us with pathogenesis and prophylaxis.

Authors:  F Stapleton; N Carnt
Journal:  Eye (Lond)       Date:  2011-12-02       Impact factor: 3.775

Review 6.  Proteases, cystic fibrosis and the epithelial sodium channel (ENaC).

Authors:  P H Thibodeau; M B Butterworth
Journal:  Cell Tissue Res       Date:  2012-05-22       Impact factor: 5.249

7.  FlhA, a component of the flagellum assembly apparatus of Pseudomonas aeruginosa, plays a role in internalization by corneal epithelial cells.

Authors:  S M Fleiszig; S K Arora; R Van; R Ramphal
Journal:  Infect Immun       Date:  2001-08       Impact factor: 3.441

8.  Impact of heterogeneity within cultured cells on bacterial invasion: analysis of Pseudomonas aeruginosa and Salmonella enterica serovar typhi entry into MDCK cells by using a green fluorescent protein-labelled cystic fibrosis transmembrane conductance regulator receptor.

Authors:  A A Gerçeker; T Zaidi; P Marks; D E Golan; G B Pier
Journal:  Infect Immun       Date:  2000-02       Impact factor: 3.441

9.  Epithelial cell polarity alters Rho-GTPase responses to Pseudomonas aeruginosa.

Authors:  Barbara I Kazmierczak; Keith Mostov; Joanne N Engel
Journal:  Mol Biol Cell       Date:  2003-10-31       Impact factor: 4.138

10.  Pseudomonas aeruginosa-mediated damage requires distinct receptors at the apical and basolateral surfaces of the polarized epithelium.

Authors:  Iwona Bucior; Keith Mostov; Joanne N Engel
Journal:  Infect Immun       Date:  2009-12-14       Impact factor: 3.441

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