A Novel Exopolysaccharide from the Biofilm of Thermus aquaticus YT-1 Induces the Immune Response through Toll-like Receptor 2

被引:56
作者
Lin, Miao-Hsia [2 ]
Yang, Yu-Liang [2 ]
Chen, Yen-Po [1 ]
Hua, Kuo-Feng [3 ]
Lu, Chun-Ping [2 ]
Sheu, Fuu [4 ]
Lin, Guang-Huey [5 ]
Tsay, San-San [6 ,7 ]
Liang, Shu-Mei [1 ]
Wu, Shih-Hsiung [2 ]
机构
[1] Acad Sinica, Agr Biotechnol Res Ctr, Taipei 115, Taiwan
[2] Acad Sinica, Inst Biol Chem, Taipei 115, Taiwan
[3] Natl Ilan Univ, Inst Biotechnol, Ilan 260, Taiwan
[4] Natl Taiwan Univ, Dept Hort, Taipei 106, Taiwan
[5] Tzu Chi Univ, Inst Microbiol Immunol & Mol Med, Hualien 970, Taiwan
[6] Natl Taiwan Univ, Dept Life Sci, Taipei 106, Taiwan
[7] Natl Taiwan Univ, Inst Plant Biol, Taipei 106, Taiwan
关键词
EXTREME THERMOPHILE; CYTOKINE PRODUCTION; IN-VIVO; PATHOGEN RECOGNITION; DENDRITIC CELLS; INNATE IMMUNITY; POLYSACCHARIDES; IDENTIFICATION; MACROPHAGES; INDUCTION;
D O I
10.1074/jbc.M110.200113
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacterial polysaccharides are known to induce the immune response in macrophages. Here we isolated a novel extracellular polysaccharide from the biofilm of Thermus aquaticus YT-1 and evaluated its structure and immunomodulatory effects. The size of this polysaccharide, TA-1, was deduced by size-exclusion chromatography as 500 kDa. GC-MS, high performance anion-exchange chromatography with pulsed amperometric detection, electrospray ionization-MS/MS, and NMR revealed the novel structure of TA-1. The polysaccharide is composed of tetrasaccharide-repeating units of galactofuranose, galactopyranose, and N-acetylgalactosamine (1: 1: 2) and lacked acidic sugars. TA-1 stimulated macrophage cells to produce the cytokines TNF-alpha and IL-6. Screening of Toll-like receptors and antibody-blocking experiments indicated that the natural receptor of TA-1 in its immunoactivity is TLR2. Recognition of TA-1 by TLR2 was confirmed by TA-1 induction of IL-6 production in peritoneal macrophages from wild-type mice but not from TLR2 (-/-) mice. TA-1, as a TLR2 agonist, could possibly be used as an adjuvant and could enhance cytokine release, which increases the immune response. Furthermore, TA-1 induced cytokine release is dependent on MyD88/TIRAP.
引用
收藏
页码:17736 / 17745
页数:10
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