Regulation of epidermal tight-junctions (TJ) during infection with exfoliative toxin-negative Staphylococcus strains.

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Regulation of epidermal tight-junctions (TJ) during infection with exfoliative toxin-negative Staphylococcus strains. / Ohnemus, Ullrich; Kohrmeyer, Klaas; Houdek, Pia; Rohde, Holger; Wladykowski, Ewa; Vidal, Sabine; Horstkotte, Matthias A.; Aepfelbacher, Martin; Kirschner, Nina; Behne, Martin; Moll, Ingrid; Brandner, Johanna.

in: J INVEST DERMATOL, Jahrgang 128, Nr. 4, 4, 2008, S. 906-916.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Ohnemus, U, Kohrmeyer, K, Houdek, P, Rohde, H, Wladykowski, E, Vidal, S, Horstkotte, MA, Aepfelbacher, M, Kirschner, N, Behne, M, Moll, I & Brandner, J 2008, 'Regulation of epidermal tight-junctions (TJ) during infection with exfoliative toxin-negative Staphylococcus strains.', J INVEST DERMATOL, Jg. 128, Nr. 4, 4, S. 906-916. <http://www.ncbi.nlm.nih.gov/pubmed/17914452?dopt=Citation>

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Vancouver

Bibtex

@article{6e03e6adbf394223bc93919f670b2691,
title = "Regulation of epidermal tight-junctions (TJ) during infection with exfoliative toxin-negative Staphylococcus strains.",
abstract = "Tight Junction (TJ) proteins have been shown to exert a barrier function within the skin. Here, we study the fate of TJ proteins during the challenge of the skin by bacterial colonization and infection. We investigated the influence of various exfoliative toxin-negative Staphylococcus strains on TJ, adherens junction (AJ), desmosomal proteins, and actin in a human keratinocyte infection culture and in a porcine skin infection model. We found that the pathogen Staphylococcus aureus downregulates TJ and subsequently AJ and desmosomal proteins, including atypical protein kinase C, an essential player in TJ formation, at the cell-cell borders of keratinocytes in a time and concentration dependent manner. Little changes in protein and RNA levels were seen, indicating redistribution of proteins. In cultured keratinocytes, a reduction of transepithelial resistance was observed. Staphylococcus epidermidis shows only minor effects. All strains induced enhanced expression of occludin and ZO-1 at the beginning of colonization/infection. Thus, we demonstrate that TJ are likely to be involved in skin infection of exfoliative toxin-negative S. aureus. As we did not find a change in actin, and as changes of TJ preceded alterations of AJs and desmosomes, we suggest that S. aureus targets TJ.",
author = "Ullrich Ohnemus and Klaas Kohrmeyer and Pia Houdek and Holger Rohde and Ewa Wladykowski and Sabine Vidal and Horstkotte, {Matthias A.} and Martin Aepfelbacher and Nina Kirschner and Martin Behne and Ingrid Moll and Johanna Brandner",
year = "2008",
language = "Deutsch",
volume = "128",
pages = "906--916",
journal = "J INVEST DERMATOL",
issn = "0022-202X",
publisher = "NATURE PUBLISHING GROUP",
number = "4",

}

RIS

TY - JOUR

T1 - Regulation of epidermal tight-junctions (TJ) during infection with exfoliative toxin-negative Staphylococcus strains.

AU - Ohnemus, Ullrich

AU - Kohrmeyer, Klaas

AU - Houdek, Pia

AU - Rohde, Holger

AU - Wladykowski, Ewa

AU - Vidal, Sabine

AU - Horstkotte, Matthias A.

AU - Aepfelbacher, Martin

AU - Kirschner, Nina

AU - Behne, Martin

AU - Moll, Ingrid

AU - Brandner, Johanna

PY - 2008

Y1 - 2008

N2 - Tight Junction (TJ) proteins have been shown to exert a barrier function within the skin. Here, we study the fate of TJ proteins during the challenge of the skin by bacterial colonization and infection. We investigated the influence of various exfoliative toxin-negative Staphylococcus strains on TJ, adherens junction (AJ), desmosomal proteins, and actin in a human keratinocyte infection culture and in a porcine skin infection model. We found that the pathogen Staphylococcus aureus downregulates TJ and subsequently AJ and desmosomal proteins, including atypical protein kinase C, an essential player in TJ formation, at the cell-cell borders of keratinocytes in a time and concentration dependent manner. Little changes in protein and RNA levels were seen, indicating redistribution of proteins. In cultured keratinocytes, a reduction of transepithelial resistance was observed. Staphylococcus epidermidis shows only minor effects. All strains induced enhanced expression of occludin and ZO-1 at the beginning of colonization/infection. Thus, we demonstrate that TJ are likely to be involved in skin infection of exfoliative toxin-negative S. aureus. As we did not find a change in actin, and as changes of TJ preceded alterations of AJs and desmosomes, we suggest that S. aureus targets TJ.

AB - Tight Junction (TJ) proteins have been shown to exert a barrier function within the skin. Here, we study the fate of TJ proteins during the challenge of the skin by bacterial colonization and infection. We investigated the influence of various exfoliative toxin-negative Staphylococcus strains on TJ, adherens junction (AJ), desmosomal proteins, and actin in a human keratinocyte infection culture and in a porcine skin infection model. We found that the pathogen Staphylococcus aureus downregulates TJ and subsequently AJ and desmosomal proteins, including atypical protein kinase C, an essential player in TJ formation, at the cell-cell borders of keratinocytes in a time and concentration dependent manner. Little changes in protein and RNA levels were seen, indicating redistribution of proteins. In cultured keratinocytes, a reduction of transepithelial resistance was observed. Staphylococcus epidermidis shows only minor effects. All strains induced enhanced expression of occludin and ZO-1 at the beginning of colonization/infection. Thus, we demonstrate that TJ are likely to be involved in skin infection of exfoliative toxin-negative S. aureus. As we did not find a change in actin, and as changes of TJ preceded alterations of AJs and desmosomes, we suggest that S. aureus targets TJ.

M3 - SCORING: Zeitschriftenaufsatz

VL - 128

SP - 906

EP - 916

JO - J INVEST DERMATOL

JF - J INVEST DERMATOL

SN - 0022-202X

IS - 4

M1 - 4

ER -