Gegner J A, Ulevitch R J, Tobias P S
Department of Immunology, Scripps Research Institute, La Jolla, California 92037.
J Biol Chem. 1995 Mar 10;270(10):5320-5. doi: 10.1074/jbc.270.10.5320.
Under physiological conditions, lipopolysaccharide (LPS) activation of cells involves the LPS binding protein (LBP) and either membrane or soluble CD14. We find LPS forms a ternary complex with LBP and membrane CD14 (mCD14). Subsequent to complex formation and distinct from signal transduction, LBP and LPS internalize. Internalization can be separated from signal transduction with the anti-LBP antibody 18G4 and the anti-CD14 antibody 18E12. 18G4 inhibits LBP binding to mCD14 without blocking signal transduction or LPS transfer to soluble CD14; 18E12 inhibits signal transduction without affecting LPS binding and uptake. These data show that while LPS signal transduction and LPS clearance utilize both LBP and mCD14, the pathways bifurcate after LPS binding to mCD14.
在生理条件下,细胞的脂多糖(LPS)激活涉及脂多糖结合蛋白(LBP)以及膜型或可溶性CD14。我们发现LPS与LBP和膜型CD14(mCD14)形成三元复合物。复合物形成后且不同于信号转导,LBP和LPS会内化。内化过程可以通过抗LBP抗体18G4和抗CD14抗体18E12与信号转导分开。18G4抑制LBP与mCD14的结合,而不阻断信号转导或LPS向可溶性CD14的转移;18E12抑制信号转导,而不影响LPS的结合和摄取。这些数据表明,虽然LPS信号转导和LPS清除都利用LBP和mCD14,但在LPS与mCD14结合后,这两条途径会分叉。