Endotoxic Properties of Chemically Synthesized Lipid A Analogs
Biological activities of two groups of synthesized lipid A analogs, the counterpart of biosynthetic precursor, Lehmann's Ia type, 406, and E. coli lipid A type, 506, as well as their non‐phosphorylated, and mono‐phosphorylated analogs were investigated. The activities employed included four bon...
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Published in | Microbiology and immunology Vol. 33; no. 10; pp. 797 - 810 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Blackwell Publishing Ltd
01.10.1989
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Online Access | Get full text |
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Summary: | Biological activities of two groups of synthesized lipid A analogs, the counterpart of biosynthetic precursor, Lehmann's Ia type, 406, and E. coli lipid A type, 506, as well as their non‐phosphorylated, and mono‐phosphorylated analogs were investigated. The activities employed included four bone marrow cell reactions in mice, mice skin reaction, leukocytes migration in rabbits' cornea, and hemagglutination. Compound 406 and 506 elicited bone marrow reactions in mice and hemagglutination of mouse RBC, although 406 failed to elicit hemorrhage and necrosis also in mice skin. Compound 406 did not elicit corneal reaction in rabbits. The results suggest that for elicitation of this reaction and mice skin reaction, acyloxyacyl structure is required. Cytotoxicity and thromboplastin production of four bone marrow reactions had been reported by us to be endotoxic reactions, since these had not been elicited by peptidoglycan of Lactobacillus and Staphylococcus (1981) and 300 series synthetized analogs (1984) which did not have endotoxic structures. From these results, it seems that these two marrow reactions and hemagglutination require, as does the limulus test, the lipid A part structure as is present in 406. |
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Bibliography: | ArticleID:MIM00966 istex:ADB20A870E4D904C7D199AC0DBE831E58B9F8754 ark:/67375/WNG-HWHCMXK8-0 |
ISSN: | 0385-5600 1348-0421 |
DOI: | 10.1111/j.1348-0421.1989.tb00966.x |