Haziot A, Rong G W, Silver J, Goyert S M
North Shore University Hospital/Cornell University Medical College, Manhasset, NY 11030.
J Immunol. 1993 Aug 1;151(3):1500-7.
Recent studies have suggested that soluble CD14 found in serum is involved in the LPS-induced activation of endothelial cells (EC). To more fully investigate the relevance of sCD14 to LPS-induced activation of EC, we have used recombinant soluble CD14 (rsCD14) and have examined, under serum-free conditions, its role in the LPS-induced EC response in the presence of LPS alone as well as in the presence of LPS-binding protein. Our studies show that EC can be activated by high concentrations of LPS in the presence of rsCD14 alone. However, at low concentrations of LPS (5 and 10 ng/ml), the rsCD14-stimulated activation is strongly enhanced by LPS-binding protein. In addition, we show that LPS binds to rsCD14 directly; in the presence of low concentrations of LPS this binding is enhanced by the presence of LPS-binding protein. These results show that while the membrane form of CD14 can function as a receptor, its soluble form can function as a co-ligand with LPS in the EC-LPS response.
近期研究表明,血清中发现的可溶性CD14参与了脂多糖(LPS)诱导的内皮细胞(EC)激活过程。为了更全面地研究可溶性CD14与LPS诱导的内皮细胞激活之间的相关性,我们使用了重组可溶性CD14(rsCD14),并在无血清条件下,研究了其在单独存在LPS以及存在LPS结合蛋白的情况下,在LPS诱导的内皮细胞反应中的作用。我们的研究表明,在内皮细胞单独存在rsCD14的情况下,高浓度的LPS可激活内皮细胞。然而,在低浓度LPS(5和10 ng/ml)时,LPS结合蛋白可强烈增强rsCD14刺激的激活作用。此外,我们发现LPS可直接与rsCD14结合;在低浓度LPS存在时,LPS结合蛋白的存在可增强这种结合。这些结果表明,虽然CD14的膜形式可作为一种受体发挥作用,但其可溶性形式在EC-LPS反应中可作为LPS的共配体发挥作用。