Immunobiological activities of a chemically synthesized lipid A of Porphyromonas gingivalis

被引:25
作者
Ogawa, T
Asai, Y
Yamamoto, H
Taiji, Y
Jinno, T
Kodama, T
Niwata, S
Shimauchi, H
Ochiai, K
机构
[1] Asahi Univ, Sch Dent, Dept Oral Microbiol, Hozumi, Gifu 5010296, Japan
[2] Suntory Ltd, Inst Fundamental Res, Shimamoto, Osaka 6180012, Japan
[3] Osaka Univ, Fac Dent, Dept Periodontol & Endodontol, Suita, Osaka 5650871, Japan
[4] Nihon Univ, Sch Dent, Dept Microbiol, Chiba 2718587, Japan
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2000年 / 28卷 / 04期
关键词
synthetic lipid A; endotoxicity; C3H/HeJ mouse; macrophage; gingival fibroblast; Porphyromonas gingivalis;
D O I
10.1016/S0928-8244(00)00167-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A synthetic lipid A of Porphyromonas gingivalis strain 381 (compound PG-381), which is similar to its natural lipid A, demonstrated no or very low endotoxic activities as compared to Escherichia coli-type synthetic lipid A (compound 506). On the other hand, compound PG-381 had stronger hemagglutinating activities on rabbit erythrocytes than compound 506. Compound PG-381 also induced mitogenic responses in spleen cells from lipopolysaccharide (LPS)-hyporesponsive C3H/HeJ mice, as well as LPS-responsive C3H/HeN mice. The addition of polymyxin B resulted in the inhibition of mitogenic activities, however, compound 506 did not show these capacities, Additionally, compound PG-381 showed a lower level of activity in inducing cytokine production in peritoneal macrophages and gingival fibroblasts from C3H/MeN mice, but not C3H/HeJ mice, in comparison to compound 506. Thus, this study demonstrates that the chemical synthesis of lipid A, mimicking the natural lipid A portion of LPS from P. gingivalis, confirms its low endotoxic potency and immunobiological activity. (C) 2000 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:273 / 281
页数:9
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