Innate immunomodulation by lipophilic termini of lipopolysaccharide; synthesis of lipid As from Porphyromonas gingivalis and other bacteria and their immunomodulative responses

被引:29
作者
Fujimoto, Yukari [1 ]
Shimoyama, Atsushi [1 ]
Saeki, Akinori [1 ]
Kitayama, Naohiro [1 ]
Kasamatsu, Chika [1 ]
Tsutsui, Hiroko [2 ]
Fukase, Koichi [1 ]
机构
[1] Osaka Univ, Dept Chem, Grad Sch Sci, Toyonaka, Osaka 5600043, Japan
[2] Hyogo Coll Med, Dept Microbiol, Nishinomiya, Hyogo 6638501, Japan
基金
日本学术振兴会;
关键词
CORONARY-HEART-DISEASE; HELICOBACTER-PYLORI; CHLAMYDIA-PNEUMONIAE; CHEMICAL-STRUCTURE; STRUCTURAL BASIS; BACTEROIDES GINGIVALIS; TLR4-MD-2; COMPLEX; ATHEROSCLEROSIS; RECOGNITION; ENDOTOXIN;
D O I
10.1039/c3mb25477a
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
Synthetic studies of lipid A and LPS partial structures have been performed to investigate the relationship between structures and functions of LPS. Recent studies have suggested several pathological implications of LPS from parasitic bacteria due to its influence on the host immune responses. To address this issue, we established an efficient synthetic strategy that is widely applicable to the synthesis of various lipid As by using a key disaccharide intermediate with selectively cleavable protecting groups. Porphyromonas gingivalis and Helicobacter pylori lipid As were synthesized and their biological activities were evaluated. All synthetic lipid As did not induce strong inflammatory responses: some are very weak cytokine inducers and others are antagonistic in IL-6 and IL-8 induction with E. coli LPS. On the other hand, P. gingivalis lipid As showed potent IL-18 inducing activity. Since IL-18 has been shown to correlate with chronic inflammation, P. gingivalis LPS may be implicated in the chronic inflammatory responses.
引用
收藏
页码:987 / 996
页数:10
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