Journal of Biological Chemistry · 2002 · 451 citations · 36 references
Life SciencesCell BiologyImmunologyCell SignalingInnate ImmunitySignal TransductionCell-surface ReceptorsImmune Cell SignalingInflammatory Cell SignalingInflammatory SignalingMacrophage BiologyToll-like ReceptorsAggregationCell Surface Toll-like ReceptorsGolgi Apparatus LocalizationMyd88-dependent SignalingSignalingTlr TraffickingToll-like Receptor SignalingToll-like Receptor-mediated Innate Immune Response
LPS responses in mammals depend on the expression of TLR4, CD14, and MD‑2. TLR4, CD14, and MD‑2 rapidly recycle between the Golgi and plasma membrane, yet LPS signaling is initiated at the cell surface and does not require Golgi trafficking.
Mammalian responses to LPS require the expression of Toll-like receptor 4 (TLR4), CD14, and MD-2. We expressed fluorescent TLR4 in cell lines and found that TLR4 densely localized to the surface and the Golgi. Similar distributions were observed in human monocytes. Confocal imaging revealed rapid recycling of TLR4-CD14-MD-2 complexes between the Golgi and the plasma membrane. Fluorescent LPS followed these trafficking pathways in CD14-positive cells. The TLR4- adapter protein, MyD88, translocated to the cell surface upon LPS exposure, and cross-linking of surface TLR4 with antibody induced signaling. Golgi-associated TLR4 expression was disrupted by brefeldin A, yet LPS signaling was preserved. We conclude that LPS signaling may be initiated by surface aggregation of TLR4 and is not dependent upon LPS trafficking to the Golgi.
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Defective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in <i>Tlr4</i> Gene
Alexander Poltorak, Xiaolong He, Irina Smirnova et al. · Science · 1998 · 7.6K citations
Katsuaki Hoshino, Osamu Takeuchi, Taro Kawai et al. · The Journal of Immunology · 1999 · 3.4K citations · Full text
Life Sciences, Genetics, Immunology +15