Characteristics and Biological Variations of M-Ficolin, a Pattern Recognition Molecule, in Plasma

被引:101
作者
Wittenborn, Thomas [1 ]
Thiel, Steffen [1 ]
Jensen, Lisbeth [1 ]
Nielsen, Hans J. [2 ]
Jensenius, Jens C. [1 ]
机构
[1] Univ Aarhus, Dept Med Microbiol & Immunol, DK-8000 Aarhus C, Denmark
[2] Univ Copenhagen, Dept Surg Gastroenterol, Hvidovre Hosp, Copenhagen, Denmark
基金
英国医学研究理事会;
关键词
Complement system; Host defense; In vitro assays; M-ficolin; Pathogen-associated molecular patterns; Pattern recognition molecules; Protein identification; Protein purification; MANNAN-BINDING LECTIN; HAKATA ANTIGEN; FIBRINOGEN-LIKE; COMPLEMENT PATHWAY; APOPTOTIC CELLS; INNATE IMMUNITY; ACETYL GROUPS; H-FICOLIN; CLONING; PROTEIN;
D O I
10.1159/000218324
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The three human ficolins, H-ficolin, L-ficolin and M-ficolin, are pattern recognition molecules of the innate immune system. All three ficolins can activate the lectin pathway of the complement system after binding to pathogens. H- and L-ficolin are serum proteins with an average concentration of 18 and 3 mu g/ml, respectively. M-ficolin has been described as a membrane-associated pattern recognition receptor of monocytes, being also present in granulocytes; recently, minuscule amounts of M-ficolin have been found in serum, too. No assay specific for M-ficolin has yet been described and biological variations are unknown. We have raised specific monoclonal anti-human M-ficolin antibodies and have developed a quantitative assay for M-ficolin. M-ficolin elutes as a large, 900-kDa protein upon gel permeation chromatography of serum. Analysis of M-ficolin levels in serum samples of 350 blood donors reveals a mean concentration of 1.07 mu g/ml, ranging from 0.28 to 4.05 mu g/ml. Analyses of consecutive acute phase serum samples from major surgery patients indicated a complex response. Ontogeny was investigated through cord blood samples from healthy full-term babies, which showed adult levels, with sequential samples showing no increase from birth to 1 year of age. We suggest that M-ficolin should also be considered as a humoral pattern recognition molecule. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:167 / 180
页数:14
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