Cutting edge: cell surface expression and lipopolysaccharide signaling via the toll-like receptor 4-MD-2 complex on mouse peritoneal macrophages

S Akashi, R Shimazu, H Ogata, Y Nagai… - The Journal of …, 2000 - journals.aai.org
S Akashi, R Shimazu, H Ogata, Y Nagai, K Takeda, M Kimoto, K Miyake
The Journal of Immunology, 2000journals.aai.org
The human MD-2 molecule is associated with the extracellular domain of human Toll-like
receptor 4 (TLR4) and greatly enhances its LPS signaling. The human TLR4-MD-2 complex
thus signals the presence of LPS. Little is known, however, about cell surface expression
and LPS signaling of the TLR4-MD-2 complex in vivo. We cloned mouse MD-2 molecularly
and established a unique mAb MTS510, which reacted selectively with mouse TLR4-MD-2
but not with TLR4 alone in flow cytometry. Mouse MD-2 expression in TLR4-expressing cells …
Abstract
The human MD-2 molecule is associated with the extracellular domain of human Toll-like receptor 4 (TLR4) and greatly enhances its LPS signaling. The human TLR4-MD-2 complex thus signals the presence of LPS. Little is known, however, about cell surface expression and LPS signaling of the TLR4-MD-2 complex in vivo. We cloned mouse MD-2 molecularly and established a unique mAb MTS510, which reacted selectively with mouse TLR4-MD-2 but not with TLR4 alone in flow cytometry. Mouse MD-2 expression in TLR4-expressing cells enhanced LPS-induced NF-κB activation, which was clearly inhibited by MTS510. Thioglycolate-elicited peritoneal macrophages expressed TLR4-MD-2, which was rapidly down-regulated in the presence of LPS. Moreover, LPS-induced TNF-α production by peritoneal macrophages was inhibited by MTS510. Collectively, the TLR4-MD-2 complex is expressed on macrophages in vivo and senses and signals the presence of LPS.
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