Bacterial components induce cytokine and intercellular adhesion molecules-1 and activate transcription factors in dermal fibroblasts

This study investigated the effect of various structural components of Gram-positive (lipotheichoic acid and protein A) and Gram-negative (porins and lipopolysaccharide) bacteria on human dermal fibroblasts. Fibroblasts are important effector cells which have a potential role in augmenting the infla...

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Published inResearch in microbiology Vol. 154; no. 5; pp. 337 - 344
Main Authors Perfetto, Brunella, Donnarumma, Giovanna, Criscuolo, Daniela, Paoletti, Iole, Grimaldi, Elena, Tufano, Maria Antonietta, Baroni, Adone
Format Journal Article
LanguageEnglish
Published Paris Elsevier SAS 01.06.2003
Elsevier
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Summary:This study investigated the effect of various structural components of Gram-positive (lipotheichoic acid and protein A) and Gram-negative (porins and lipopolysaccharide) bacteria on human dermal fibroblasts. Fibroblasts are important effector cells which have a potential role in augmenting the inflammatory response in various diseases. In this study we present a profile of TNF-α, IL-6 and IL-8, the expression of intercellular adhesion molecules (ICAM-1) and the activation of transcriptional nuclear factor NF-kB and AP-1 in human dermal fibroblasts stimulated by bacterial surface components. Compared to the controls, increased ICAM–1, IL-6 and IL-8 gene expression after stimulation of LPS and porins at 2 and 4 h was more evident than that obtained following stimulation of LTA and PA. Gene expression was also associated with the production of cytokine proteins in culture supernatants. TNF-α gene expression remained undetectable. Moreover, LPS and porin treatments determined IkBα phosphorylation and degradation in human dermal fibroblasts and the subsequent activation of nuclear factors NF-kB and AP-1. These data suggest the importance of such stimuli in the first step of the inflammatory process, as well as the important role played by fibroblasts in skin inflammatory disease.
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ISSN:0923-2508
1769-7123
DOI:10.1016/S0923-2508(03)00084-6