## Abstract Microglia are activated by lipopolysaccharide (LPS) to produce neurotoxic pro‐inflammatory factors and reactive oxygen species (ROS). While a multitude of LPS receptors and corresponding pathways have been identified, the detailed mechanisms mediating the microglial response to LPS are
Toll-like receptor 4 expression levels determine the degree of LPS-susceptibility in mice
✍ Scribed by Christoph Kalis; Benoit Kanzler; Annalisa Lembo; Alexander Poltorak; Chris Galanos; Marina A. Freudenberg
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 202 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0014-2980
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
C57BL/10ScCr (Cr) mice carry a deletion of the Toll‐like receptor 4 (tlr4) gene (i.e. they are tlr4^0/0^) and are thus refractory to LPS effects. Insertion of wild‐type tlr4 transgene into the tlr4^0/0^ Cr germ line endowed LPS susceptibility in the two transgenic lines created, indicating that TLR4 is the only limiting factor for LPS responsiveness in Cr mice. The absolute levels of tlr4 mRNA expressed by the heterozygous transgenic (tlr4^Tr/0^), wild‐type C57BL/10ScSn (Sn) (tlr4^+/+^) and heterozygous F1 (Sn × Cr) (tlr4^+/0^) mice varied markedly. However, the pattern of distribution of expression in the different organs was the same in all strains. In different biological assays (B cell mitogenicity, cytokine induction and lethal toxicity) the degree of LPS response obtained in the different strains of mice correlated with the levels of tlr4 mRNA expression. In macrophages, investigation of the LPS‐induced cytokine (IL‐6) response revealed a linear relationship between the response and the logarithm of TLR4–MD‐2 levels.
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