Literature DB >> 7683322

Endotoxin-induced expression of endotoxin binding sites on murine bone marrow cells.

R Girard1, T Pedron, R Chaby.   

Abstract

A variety of binding sites for endotoxin (LPS) have been identified on leukocytes. However, the sequence of expression of these receptors, and their interrelations, are poorly understood. In this report, we show that in LPS-responsive hosts, interaction of nanomolar concentrations of LPS with bone marrow cells induces the expression of new specific LPS-binding sites. Cells from LPS-nonresponsive (C3H/HeJ) mice do not express these receptors after LPS treatment. Experimental differences in the conditions allowing the induction and the detection of these binding sites (influence of Leishmania lipophosphoglycan, role of serum), support the hypothesis that interaction of LPS with primary receptors on bone marrow cells triggers the expression of secondary LPS receptors, and that the two types of receptors have distinct fine specificities.

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Year:  1993        PMID: 7683322

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  8 in total

1.  Interaction of pulmonary surfactant protein C with CD14 and lipopolysaccharide.

Authors:  Luis A Augusto; Monique Synguelakis; Jan Johansson; Thierry Pedron; Robert Girard; Richard Chaby
Journal:  Infect Immun       Date:  2003-01       Impact factor: 3.441

2.  Interaction of NK lysin, a peptide produced by cytolytic lymphocytes, with endotoxin.

Authors:  M Andersson; R Girard; P Cazenave
Journal:  Infect Immun       Date:  1999-01       Impact factor: 3.441

3.  Functional lipopolysaccharide receptors of low affinity are constitutively expressed on mouse bone marrow cells.

Authors:  R Girard; T Pedron; R Chaby
Journal:  Immunology       Date:  1997-07       Impact factor: 7.397

4.  Down-modulation of L-selectin by lipopolysaccharide is not required for lipopolysaccharide-induced expression of CD14 in mouse bone marrow granulocytes.

Authors:  T Pédron; R Girard; R Chaby
Journal:  Infect Immun       Date:  2001-07       Impact factor: 3.441

5.  Involvement of the membrane form of tumour necrosis factor-alpha in lipopolysaccharide-induced priming of mouse peritoneal macrophages for enhanced nitric oxide response to lipopolysaccharide.

Authors:  P Ancuta; H Fahmi; J F Pons; K Le Blay; R Chaby
Journal:  Immunology       Date:  1997-10       Impact factor: 7.397

6.  Inability of the Francisella tularensis lipopolysaccharide to mimic or to antagonize the induction of cell activation by endotoxins.

Authors:  P Ancuta; T Pedron; R Girard; G Sandström; R Chaby
Journal:  Infect Immun       Date:  1996-06       Impact factor: 3.441

7.  The lipid A region of lipopolysaccharides from Rhizobiaceae activates bone marrow granulocytes from lipopolysaccharide-hyporesponsive C3H/HeJ and C57BL/10ScCr mice.

Authors:  T Pedron; R Girard; B Jeyaretnam; R W Carlson; R Chaby
Journal:  Immunology       Date:  2000-10       Impact factor: 7.397

8.  Preexposure of mouse peritoneal macrophages to lipopolysaccharide and other stimuli enhances the nitric oxide response to secondary stimuli.

Authors:  H Fahmi; P Ancuta; S Perrier; R Chaby
Journal:  Inflamm Res       Date:  1996-07       Impact factor: 4.575

  8 in total

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