Macrophage stimulation by bacterial lipopolysaccharides. II. Evidence for differentiation signals delivered by lipid A and by a protein rich fraction of lipopolysaccharides
- PMID: 359747
- PMCID: PMC2184939
- DOI: 10.1084/jem.148.2.557
Macrophage stimulation by bacterial lipopolysaccharides. II. Evidence for differentiation signals delivered by lipid A and by a protein rich fraction of lipopolysaccharides
Abstract
Stimulation of macrophages to lyse tumor cells is a property common to lipopolysaccharide (LPS) extracted from a variety of smooth and rough bacterial strains by several different preparative procedures. The relationship between macrophage stimulation and the structural characteristics of LPS is defined. In protein-free LPS, lipid A bears the stimulatory signal which results in the differentiation of elicited macrophages into killer cells. The polysaccharide moiety is neither stimulatory itself nor does it block the activity of complete LPS on macrophages. Extraction of LPS by the butanol or Boivin procedures produces preparations in which LPS is complexed through its lipid A moiety to a protein rich component, LAP. Isolated LAP delivers a macrophage differentiation signal which is independent of lipid A. The presence of these two structurally distinct constituents in the cell walls of gram-negative bacteria broadens the biological environments in which they can stimulate macrophages in vivo.
Similar articles
-
Production of tumor necrosis factor by rIFN-gamma-primed C3H/HeJ (Lpsd) macrophages requires the presence of lipid A-associated proteins.J Immunol. 1988 Dec 15;141(12):4196-202. J Immunol. 1988. PMID: 3143760
-
Macrophage stimulation by bacterial lipopolysaccharides. III. Selective unresponsiveness of C3H/HeJ macrophages to the lipid A differentiation signal.J Immunol. 1979 Nov;123(5):2304-10. J Immunol. 1979. PMID: 385780
-
Lipid A-associated proteins provide an alternate "second signal" in the activation of recombinant interferon-gamma-primed, C3H/HeJ macrophages to a fully tumoricidal state.J Immunol. 1987 Dec 1;139(11):3697-702. J Immunol. 1987. PMID: 3119714
-
Lipopolysaccharide receptors and signal transduction pathways in mononuclear phagocytes.Curr Top Microbiol Immunol. 1992;181:169-88. doi: 10.1007/978-3-642-77377-8_6. Curr Top Microbiol Immunol. 1992. PMID: 1385048 Review.
-
Gram-negative endotoxin: a biologically active lipid.Cold Spring Harb Symp Quant Biol. 1988;53 Pt 2:973-82. doi: 10.1101/sqb.1988.053.01.112. Cold Spring Harb Symp Quant Biol. 1988. PMID: 2474409 Review. No abstract available.
Cited by
-
Endotoxin inhibition of macrophage-mediated bone resorption.Calcif Tissue Int. 1981;33(3):269-75. doi: 10.1007/BF02409448. Calcif Tissue Int. 1981. PMID: 6791790 No abstract available.
-
Stimulation of human monocytes by endotoxin-associated protein: inhibition of programmed cell death (apoptosis) and potential significance in adjuvanticity.Infect Immun. 1992 Apr;60(4):1684-6. doi: 10.1128/iai.60.4.1684-1686.1992. Infect Immun. 1992. PMID: 1548091 Free PMC article.
-
Outer membrane protein A, peptidoglycan-associated lipoprotein, and murein lipoprotein are released by Escherichia coli bacteria into serum.Infect Immun. 2000 May;68(5):2566-72. doi: 10.1128/IAI.68.5.2566-2572.2000. Infect Immun. 2000. PMID: 10768945 Free PMC article.
-
Products of enteropathogenic Escherichia coli inhibit lymphocyte activation and lymphokine production.Infect Immun. 1995 Jun;63(6):2248-54. doi: 10.1128/iai.63.6.2248-2254.1995. Infect Immun. 1995. PMID: 7768605 Free PMC article.
-
Characterization of Limulus amoebocyte lysate-reactive material from hollow-fiber dialyzers.Appl Environ Microbiol. 1984 Dec;48(6):1189-96. doi: 10.1128/aem.48.6.1189-1196.1984. Appl Environ Microbiol. 1984. PMID: 6517586 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials