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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-kappaB 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-kappaB.