Literature DB >> 324538

Lipid A as the biologically active moiety in bacterial endotoxin (LPS)-initiated generation of procoagulant activity by peripheral blood leukocytes.

J Niemetz, D C Morrison.   

Abstract

Preparations of rabbit or human leukocytes, when incubated with bacterial endotoxins (lipopolysaccharides, LPS) are stimulated to generate a procoagulant-tissue factor activity (TFa). As LPS has been shown to consist of specific repeating oligosaccharide side chains (O-antigen) linked to a central polysaccharide core region that is, in turn, linked to the lipid region of the molecule (lipid A), we have examined the biochemical requirement of the LPS necessary for generation of TFa. Using preparations of LPS from mutant strains of bacteria, which contain varying amounts of polysaccharide in relation to lipid A, we have demonstrated that activity is associated with the lipid A region of the LPS molecule. These observations have been confirmed using isolated lipid A, which is a potent stimulator of TFa, as well as a native protoplasmic polysaccharide that is both devoid of lipid A and without detectable TFa stimulatory activity. Modification of LPS by treatment with mild alkali abrogated its capacity to stimulate TFa generation. In addition, such altered preparations of LPS partially inhibit the stimulatory effect of native LPS. Similarly, treatment of LPS (or lipid A) with the antibiotic polymyxin B substantially inhibited the stimulatory effect of LPS.

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Year:  1977        PMID: 324538

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  15 in total

1.  Expression of tissue factor procoagulant activity: regulation by cytosolic calcium.

Authors:  R Bach; D B Rifkin
Journal:  Proc Natl Acad Sci U S A       Date:  1990-09       Impact factor: 11.205

2.  Induction of procoagulant activity in human epidermal cells.

Authors:  A Schöne; E Zimmermann; J Knop
Journal:  Arch Dermatol Res       Date:  1989       Impact factor: 3.017

3.  Effect of tissue factor deficiency on mouse and tumor development.

Authors:  J R Toomey; K E Kratzer; N M Lasky; G J Broze
Journal:  Proc Natl Acad Sci U S A       Date:  1997-06-24       Impact factor: 11.205

Review 4.  The effects of bacterial endotoxins on host mediation systems. A review.

Authors:  D C Morrison; R J Ulevitch
Journal:  Am J Pathol       Date:  1978-11       Impact factor: 4.307

5.  Deleterious effects of endotoxin on cultured endothelial cells: an in vitro model of vascular injury.

Authors:  O Yamada; C F Moldow; T Sacks; P R Craddock; M A Boogaerts; H S Jacob
Journal:  Inflammation       Date:  1981-06       Impact factor: 4.092

6.  Regulation of tissue factor gene expression in the monocyte procoagulant response to endotoxin.

Authors:  S A Gregory; J H Morrissey; T S Edgington
Journal:  Mol Cell Biol       Date:  1989-06       Impact factor: 4.272

7.  Role for endotoxin in the leukocyte infiltration accompanying Escherichia coli inflammation.

Authors:  A C Issekutz; S Bhimji
Journal:  Infect Immun       Date:  1982-05       Impact factor: 3.441

8.  Regulatory roles of T mu and T gamma cells in the collaborative cellular initiation of the extrinsic coagulation pathway by bacterial lipopolysaccharide.

Authors:  G A Levy; B S Schwartz; L K Curtiss; T S Edgington
Journal:  J Clin Invest       Date:  1985-08       Impact factor: 14.808

9.  Tissue factor mRNA in THP-1 monocytic cells is regulated at both transcriptional and posttranscriptional levels in response to lipopolysaccharide.

Authors:  K Brand; B J Fowler; T S Edgington; N Mackman
Journal:  Mol Cell Biol       Date:  1991-09       Impact factor: 4.272

10.  Enhanced procoagulant activity of mononuclear leukocytes in patients with atopic dermatitis and psoriasis.

Authors:  R E Schopf; H Weber; B Morsches
Journal:  Arch Dermatol Res       Date:  1993       Impact factor: 3.017

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