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PMID: 3529396 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Detoxification of bacterial lipopolysaccharides (endotoxins) by a human neutrophil enzyme.

Science (New York, N.Y.) ·Vol. 234 ·No. 4773 ·1986-10-10 ·Pages 203-5

Munford RS, Hall CL

Abstract

Lipopolysaccharides in the cell walls of Gram-negative bacteria elicit toxic as well as potentially beneficial inflammatory responses in animals. It is now reported that tissue toxicity caused by lipopolysaccharides is preferentially reduced by an enzymatic activity in human neutrophils. Acyloxyacyl hydrolysis removes fatty acyl chains that are linked to the hydroxyl groups of 3-hydroxytetradecanoyl residues in the bioactive lipid A moiety of the lipopolysaccharides. Maximal acyloxyacyl hydrolysis reduced lipopolysaccharide tissue toxicity, as measured in the dermal Shwartzman reaction, by a factor of 100 or more. In contrast, the ability of the deacylated lipopolysaccharides to stimulate B lymphocytes to divide was decreased only by a factor of 12. It is suggested that during tissue invasion by Gram-negative bacteria acyloxyacyl hydrolysis may be a defense mechanism that reduces the toxicity of lipopolysaccharides while preserving some of their potentially beneficial inflammatory and immune stimuli.

MeSH Terms
Animals Carboxylic Ester Hydrolases/blood Humans Lipid A/metabolism,pharmacology,toxicity Lipopolysaccharides/metabolism,pharmacology,toxicity Lymphocyte Activation Neutrophils/enzymology Rabbits Salmonella typhimurium Shwartzman Phenomenon
Chemicals
Lipid A Lipopolysaccharides Carboxylic Ester Hydrolases acyloxyacyl hydrolase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Munford R S
Hall C L
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1986-10-10
Pages
203-5
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIAID NIH HHS · AI 18188 · United States
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