Abstract
Interaction of endotoxin (lipopolysaccharide [LPS]) with human lipoproteins is known to prevent the LPS-induced activation of human monocytes and release of cytokines (monokines). LPS was exposed to lipoprotein classes separated by ultracentrifugation and to apolipoprotein A-I. Then monocytes were added, and the LPS activation of monocytes was determined by measuring the induced monokines. Failure of LPS to induce monokine release was called LPS inactivation caused by lipoproteins or apolipoproteins. The LPS inactivation is shown to be a function of low-density lipoproteins. High-density lipoproteins inactivate LPS to a much lesser extent. The very-low-density lipoproteins cannot inactivate LPS. Lipid components seemed not absolutely required for LPS inactivation, because purified human apolipoprotein A-I without its physiological lipid complement also inhibits LPS-induced monokine release.
MeSH Terms
Adult
Apolipoprotein A-I/pharmacology
Blood Proteins/pharmacology
Endotoxins/antagonists & inhibitors,pharmacology
Humans
In Vitro Techniques
Interleukin-1/metabolism
Interleukin-6/metabolism
Kinetics
Lipopolysaccharides/pharmacology
Lipoproteins/antagonists & inhibitors,pharmacology
Lipoproteins, HDL/pharmacology
Lipoproteins, LDL/pharmacology
Monocytes/drug effects,immunology,metabolism
Monokines/metabolism
Tumor Necrosis Factor-alpha/metabolism
Chemicals
Apolipoprotein A-I
Blood Proteins
Cohn fraction IV
Endotoxins
Interleukin-1
Interleukin-6
Lipopolysaccharides
Lipoproteins
Lipoproteins, HDL
Lipoproteins, LDL
Monokines
Tumor Necrosis Factor-alpha
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Flegel W A
Abteilung für Transfusionsmedizin, Universität Ulm, Germany.
Baumstark M W
Weinstock C
Berg A
Northoff H
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