Lipoteichoic acid isolated from Lactobacillus plantarum inhibits lipopolysaccharide-induced TNF-alpha production in THP-1 cells and endotoxin shock in mice

• Published in: The Journal of immunology (1950) 2008-02, Vol.180 (4), p.2553-2561
• Main Authors: Kim, Han Geun, Kim, Na-Ra, Gim, Min Geun, Lee, Jung Min, Lee, Seung Yeon, Ko, Mi Yeon, Kim, Joo Yun, Han, Seung Hyun, Chung, Dae Kyun
• Format: Article
• Language: English
• Subjects: Animals; Cell Line, Tumor; Humans; Immune Tolerance - genetics; Lactobacillus plantarum; Lactobacillus plantarum - chemistry; Lactobacillus plantarum - immunology; Lipopolysaccharides - antagonists & inhibitors; Lipopolysaccharides - isolation & purification; Lipopolysaccharides - pharmacology; Male; MAP Kinase Signaling System - genetics; MAP Kinase Signaling System - immunology; Mice; Mice, Inbred BALB C; Mice, Knockout; Shock, Septic - immunology; Shock, Septic - microbiology; Shock, Septic - prevention & control; Teichoic Acids - isolation & purification; Teichoic Acids - pharmacology; Toll-Like Receptor 2 - biosynthesis; Toll-Like Receptor 2 - deficiency; Toll-Like Receptor 2 - genetics; Tumor Necrosis Factor-alpha - antagonists & inhibitors; Tumor Necrosis Factor-alpha - biosynthesis; U937 Cells
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.180.4.2553

In this study, the effect of Lactobacillus plantarum lipoteichoic acid (pLTA) on LPS-induced MAPK activation, NF-kappaB activation, and the expression of TNF-alpha and IL-1R-associated kinase M (IRAK-M) was examined. The expression of the pattern recognition receptor and the survival rate of mice were also examined. pLTA pretreatment inhibited the phosphorylation of ERK, JNK, and p38 kinase. It also inhibited the degradation of IkappaBalpha and IkappaBbeta, as well as the activation of the LPS-induced TNF-alpha factor in response to subsequent LPS stimulation. These changes were accompanied by the suppression of the LPS-induced expression of TLR4, NOD1, and NOD2, and the induction of IRAK-M, with a concurrent reduction of TNF-alpha secretion. Furthermore, the overexpression of pattern recognition receptors such as TLR4, NOD1, and NOD2 and the degradation of IRAK-M by transient transfection were found to reinstate the production of TNF-alpha after LPS restimulation. In addition, the i.p. injection of pLTA suppressed fatality, and decreased the level of TNF-alpha in the blood, in LPS-induced endotoxin shock mice. In conclusion, these data extend our understanding of the pLTA tolerance mechanism, which is related to the inhibition of LPS-induced endotoxin shock, and suggest that pLTA may have promise as a new therapeutic agent for LPS-induced septic shock.