Decay-accelerating factor (DAF/CD55) is a functional active element of the LPS receptor complex

被引:20
作者
Heine, H [1 ]
Ulmer, AJ [1 ]
El-Samalouti, VT [1 ]
Lentschat, A [1 ]
Hamann, L [1 ]
机构
[1] Res Ctr Borstel, Ctr Med & Biosci, D-23845 Borstel, Germany
来源
JOURNAL OF ENDOTOXIN RESEARCH | 2001年 / 7卷 / 03期
关键词
D O I
10.1177/09680519010070030601
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previously, we identified an 80 kDa membrane protein (LMP80) that is capable of binding to LPS and lipid A in the presence of LBP and sCD14. LMP80 could also be detected after immuno-coprecipitation of cell membranes with LPS and lipid A, indicating a physical contact of LMP80 and LPS/lipid A. Further analysis and peptide sequencing revealed that LMP80 is identical to CD55 (decay accelerating factor, DAF), a regulatory molecule of the complement cascade. Transfection of LPS-hyporesponsive Chinese hamster ovary (CHO) cells with human CD55 resulted in the translocation of NF-kappaB upon stimulation with LPS or lipid A. Our results demonstrate a new functional role of CD55 as a molecule able to mediate LPS-induced activation of cells that may be part of a multimeric LPS receptor complex.
引用
收藏
页码:227 / 231
页数:5
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