Lipoteichoic acid from Lactobacillus plantarum elicits both the production of Interleukin-23p19 and suppression of pathogen-mediated Interleukin-10 in THP-1 cells

In this study, the stimulatory effects of different lactic acid bacteria strains, and their subcellular fractions, on the THP-1 cell line were evaluated. Lactobacillus plantarum was found in particular to induce high levels of IL-23p19 mRNA, but it moderately induced TNF-α production. IL-10 producti...

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Published inFEMS immunology and medical microbiology Vol. 49; no. 2; pp. 205 - 214
Main Authors Kim, Han Geun, Gim, Min Geun, Kim, Joo Yun, Jin Hwang, Hyun, Ham, Min Seok, Lee, Jung Min, Hartung, Thomas, Park, Jung Woo, Han, Seung Hyun, Chung, Dae Kyun
Format Journal Article
LanguageEnglish
Published Oxford, UK Oxford, UK : Blackwell Publishing Ltd 01.03.2007
Blackwell Publishing Ltd
Blackwell
Oxford University Press
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Summary:In this study, the stimulatory effects of different lactic acid bacteria strains, and their subcellular fractions, on the THP-1 cell line were evaluated. Lactobacillus plantarum was found in particular to induce high levels of IL-23p19 mRNA, but it moderately induced TNF-α production. IL-10 production was not entirely affected by L. plantarum stimulation. When subcellular fractions of L. plantarum were used to treat THP-1 cells, IL-23p19 mRNA expression was enhanced in a dose-responsive manner, specifically by lipoteichoic acid (LTA). The cotreatment of THP-1 cells by both L. plantarum and Staphylococcus aureus LTA resulted in decreased IL-10 production when compared with cells treated by S. aureus LTA alone. Taken together, these data suggest that LTA isolated from L. plantarum elicits stimulatory effects upon the expression of IL-23p19 and inhibitory effects on pathogen-mediated IL-10 production.
Bibliography:http://dx.doi.org/10.1111/j.1574-695X.2006.00175.x
Editor: Artur Ulmer
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0928-8244
1574-695X
2049-632X
DOI:10.1111/j.1574-695X.2006.00175.x