MICROBIOLOGY and IMMUNOLOGY
Online ISSN : 1348-0421
Print ISSN : 0385-5600
ISSN-L : 0385-5600
Endotoxic Properties of Chemically Synthesized Lipid A Analogs
Studies on Six Inflammatory Reactions in vivo, and One Reaction in vitro
Masao YOSHIDAMichimasa HIRATAKatsuya INADANobuko TSUNODATeruo KIRIKAETsuyoshi ONODERAYoshihito ISHIKAWAOsamu SASAKITetsuo SHIBAShoichi KUSUMOTOChris GALANOSOtto LÜDERITZSeiichi KONDOKazuhito HISATSUNE
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JOURNAL FREE ACCESS

1989 Volume 33 Issue 10 Pages 797-810

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Abstract

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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