Thiel Steffen
Department of Medical Microbiology and Immunology, University of Aarhus, Wilhelms Meyers Allé, 8000 Aarhus C, Denmark.
Mol Immunol. 2007 Sep;44(16):3875-88. doi: 10.1016/j.molimm.2007.06.005.
Mannan-binding lectin (MBL), L-ficolin, M-ficolin and H-ficolin are all complement activating soluble pattern recognition molecules with recognition domains linked to collagen-like regions. All four may form complexes with four structurally related proteins, the three MBL-associated serine proteases (MASPs), MASP-1, MASP-2 and MASP-3, and a smaller MBL-associated protein (MAp19). The four recognition molecules recognize patterns of carbohydrate or acetyl-group containing ligands. After binding to the relevant targets all four are able to activate the complement system. We thus have a system where four different and/or overlapping patterns of microbial origin or patterns of altered-self may be recognized, but in all cases the signalling molecules, the MASPs, are shared. MASP-1 and MASP-3 are formed from one gene, MASP1/3, by alternative splicing generating two different mRNAs from a single primary transcript. Similarly MASP-2 and MAp19 are both generated from one gene, MASP-2/MAp19, by alternative splicing. A number of non-synonymous polymorphisms of the four recognition molecules and of the MASPs are known, and the implications of these alterations are being studied. The clinical impact of deficiencies will be discussed.
甘露聚糖结合凝集素(MBL)、L-纤维胶凝蛋白、M-纤维胶凝蛋白和H-纤维胶凝蛋白均为可激活补体的可溶性模式识别分子,其识别结构域与胶原样区域相连。这四种分子均可与四种结构相关蛋白形成复合物,即三种MBL相关丝氨酸蛋白酶(MASP)——MASP-1、MASP-2和MASP-3,以及一种较小的MBL相关蛋白(MAp19)。这四种识别分子可识别含碳水化合物或乙酰基配体的模式。与相关靶标结合后,这四种分子均能够激活补体系统。因此,我们拥有这样一个系统:可识别四种不同和/或重叠的微生物来源模式或自身改变模式,但在所有情况下,信号分子MASP是共享的。MASP-1和MASP-3由一个基因MASP1/3通过可变剪接形成,从单一初级转录本产生两种不同的mRNA。同样,MASP-2和MAp19均由一个基因MASP-2/MAp19通过可变剪接产生。已知这四种识别分子和MASP存在一些非同义多态性,目前正在研究这些改变的影响。将讨论缺陷的临床影响。