Evaluation of CD14 in host defence
- 1 February 2000
- journal article
- review article
- Published by Wiley in European Journal of Clinical Investigation
- Vol. 30 (2) , 167-179
- https://doi.org/10.1046/j.1365-2362.2000.00610.x
Abstract
An extensive search for the cell membrane targets for lipopolysaccharide (LPS), the major causative agent of Gram-negative septic shock, resulted in the identification of CD14 as the major endotoxin ‘receptor’. Besides recognition of LPS, several new aspects of its biological functions have been described recently. In this review the different CD14 forms, their most important biological and biochemical features, signalling properties, cellular and subcellular distribution and association with different diseases are discussed in detail, showing that these molecules posses several unique biological functions and further proving their central role in innate immunity.Keywords
This publication has 92 references indexed in Scilit:
- GPI-microdomains: a role in signalling via immunoreceptorsImmunology Today, 1999
- Endotoxin-tolerant Mice Have Mutations in Toll-like Receptor 4 (Tlr4)The Journal of Experimental Medicine, 1999
- Molecular Basis of Endotoxin ToleranceaAnnals of the New York Academy of Sciences, 1998
- Elevated soluble CD14 receptors and altered cytokines in chronic heart failureThe American Journal of Cardiology, 1997
- Increased in vitro production and serum levels of the soluble lipopolysaccharide receptor sCD14 in liver diseaseJournal of Hepatology, 1995
- Does endotoxin stimulate cells by mimicking ceramide?Immunology Today, 1995
- Soluble lipopolysaccharide receptor (CD14) is released via two different mechanisms from human monocytes and CD14 transfectantsEuropean Journal of Immunology, 1995
- Lipopolysaccharide Primes Human Basophils for Enhanced Mediator Release: Requirement for Plasma Co-factor and CD14Biochemical and Biophysical Research Communications, 1994
- CD14: Cell surface receptor and differentiation markerImmunology Today, 1993
- GPI-Anchored Cell-Surface Molecules Complexed to Protein Tyrosine KinasesScience, 1991