Evidence that the receptor for soluble CD14:LPS complexes may not be the putative signal-transducing molecule associated with membrane-bound CD14.
Evidence that the receptor for soluble CD14:LPS complexes may not be the putative signal-transducing molecule associated with membrane-bound CD14.
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有证据表明,可溶性 CD14:LPS 复合物的受体可能不是与膜结合 CD14 相关的推定信号转导分子。
DOI:
10.1046/j.1365-3083.1997.d01-124.x
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发表时间:
1997
影响因子:
3.7
通讯作者:
Goyert,SM
中科院分区:
文献类型:
--
作者:
Haziot,A;Katz,I;Rong,GW;Lin,XY;Silver,J;Goyert,SM
Membrane‐bound CD14 acts as a receptor for lipopolysaccharide (LPS) on monocytes/macrophages and neutrophils. Studies have suggested that the activation of monocytes/macrophages by the binding of LPS to membrane‐bound CD14 may require the association of a signal‐transducing molecule with membrane‐bound CD14. The observation that non‐CD14 expressing cells, such as endothelial cells, can nevertheless be activated by a complex of LPS and a soluble form of CD14 (sCD14) suggests that the receptor for this complex may be identical to the signal transducing molecule associated with membrane‐bound CD14. The studies described show that two CD14‐specific MoAb are able to block the LPS‐induced activation of endothelial cells but do not affect the response of monocytes to LPS. This suggests that the interaction of the sCD14:LPS complex with endothelial cells is distinct from the interaction of membrane‐bound CD14 with its putative signal‐transducing molecule.