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PMID: 8426091 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Selective refractoriness of macrophages to endotoxin-induced production of tumor necrosis factor, elicited by an autocrine mechanism.

Journal of leukocyte biology ·Vol. 53 ·No. 1 ·1993-01-00 ·Pages 45-52

Fahmi H, Chaby R

Abstract

Tolerance of macrophages to endotoxin (lipopolysaccharide, LPS) can be induced in vitro by LPS itself. We show here that one of the mechanisms of tolerance to LPS can be mediated via an autocrine process. Continuous exposure to LPS is not required to induce macrophage desensitization. Refractoriness to production of tumor necrosis factor (TNF) in response to LPS can be transferred from tolerant to naive macrophage populations by incubation of the latter with the culture supernatant of the former, in the absence of endotoxin. The active factor present in this macrophage-desensitizing culture supernatant (MD-Sup) is more efficiently removed by incubation with tolerant macrophages than by incubation with naive macrophages. The refractoriness elicited by treatment with MD-Sup is restricted to a decreased TNF response to LPS; interleukin-1 (IL-1) and IL-6 responses are not affected.

MeSH Terms
Animals Bordetella pertussis Cell Line Cells, Cultured Culture Media Dose-Response Relationship, Drug Endotoxins/pharmacology Escherichia coli Interleukin-1/biosynthesis Interleukin-6/biosynthesis Kinetics Lipopolysaccharides/pharmacology Macrophages/drug effects,physiology Mice Mice, Inbred C3H Time Factors Tumor Necrosis Factor-alpha/biosynthesis
Chemicals
Culture Media Endotoxins Interleukin-1 Interleukin-6 Lipopolysaccharides Tumor Necrosis Factor-alpha
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Fahmi H
Equipe Endotoxines, URA-1116 du Centre National de la Recherche Scientifique, Université de Paris-Sud, Orsay, France.
Chaby R
Article Info
Journal
Journal of leukocyte biology
Abbr.
J Leukoc Biol
ISSN
0741-5400
Published
1993-01-00
Pages
45-52
Language
English
Region
United States
NLM ID
8405628
Subset
IM
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