[PDF][PDF] Unresponsiveness of MyD88-deficient mice to endotoxin

T Kawai, O Adachi, T Ogawa, K Takeda, S Akira - Immunity, 1999 - cell.com
T Kawai, O Adachi, T Ogawa, K Takeda, S Akira
Immunity, 1999cell.com
MyD88 is a general adaptor protein that plays an important role in the Toll/IL-1 receptor
family signalings. Recently, Toll-like receptors 2 and 4 (TLR2 and TLR4) have been
suggested to be the signaling receptors for lipopolysaccharide (LPS). In this study, we
demonstrate that MyD88 knockout mice lack the ability to respond to LPS as measured by
shock response, B cell proliferative response, and secretion of cytokines by macrophages
and embryonic fibroblasts. However, activation of neither NF-κB nor the mitogen-activated …
Abstract
MyD88 is a general adaptor protein that plays an important role in the Toll/IL-1 receptor family signalings. Recently, Toll-like receptors 2 and 4 (TLR2 and TLR4) have been suggested to be the signaling receptors for lipopolysaccharide (LPS). In this study, we demonstrate that MyD88 knockout mice lack the ability to respond to LPS as measured by shock response, B cell proliferative response, and secretion of cytokines by macrophages and embryonic fibroblasts. However, activation of neither NF-κB nor the mitogen-activated protein (MAP) kinase family is abolished in MyD88 knockout mice. These findings demonstrate that signaling via MyD88 is essential for LPS response, but the inability of MyD88 knockout mice to induce LPS-dependent gene expression cannot simply be attributed to lack of the activation of MAP kinases and NF-κB.
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