Evidence of a trimolecular complex involving LPS, LPS binding protein and soluble CD14 as an effector of LPS response (Q28213451)

4

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author name string

Celestine J Thomas

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Mili Kapoor

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Shilpi Sharma

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Umit Zyilan

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Dan Lipsker

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Daniel Hanau

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Avadhesha Surolia

Recognition of gram-negative bacteria and endotoxin by the innate immune system

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language of work or name

English

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publication date

6 November 2002

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published in

FEBS Letters

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volume

531

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issue

2

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page(s)

184-8

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cites work

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Transfection of CD14 into 70Z/3 cells dramatically enhances the sensitivity to complexes of lipopolysaccharide (LPS) and LPS binding protein

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Soluble CD14 participates in the response of cells to lipopolysaccharide

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Lipopolysaccharide (LPS)-binding protein accelerates the binding of LPS to CD14.

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Lipopolysaccharide activation of human endothelial and epithelial cells is mediated by lipopolysaccharide-binding protein and soluble CD14

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Lipopolysaccharide is in close proximity to each of the proteins in its membrane receptor complex. transfer from CD14 to TLR4 and MD-2

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Lipopolysaccharide (LPS) signal transduction and clearance. Dual roles for LPS binding protein and membrane CD14.

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Large scale isolation of human blood monocytes by continuous flow centrifugation leukapheresis and counterflow centrifugation elutriation for adoptive cellular immunotherapy in cancer patients

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Picogram-sensitive assay for endotoxin: Gelation of Limulus polyphemus blood cell lysate induced lipopolysaccharides and lipid A from gram-negative bacteria

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inferred from DOI database lookup

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based on heuristic

Soluble CD14 activates monocytic cells independently of lipopolysaccharide

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