The house dust mite allergen Der p1 catalytically inactivates alpha(1)-antitrypsin by specific reactive centre loop cleavage: A mechanism that promotes airway inflammation and asthma

被引:80
作者
Kalsheker, NA
Deam, S
Chambers, L
Sreedharan, S
Brocklehurst, K
Lomas, DA
机构
[1] UNIV LONDON QUEEN MARY & WESTFIELD COLL,LAB STRUCT & MECHANIST ENZYMOL,DEPT BIOCHEM,LONDON E1 4NS,ENGLAND
[2] UNIV CAMBRIDGE,CTR MRC,DEPT MED,CAMBRIDGE CB2 2QH,ENGLAND
[3] UNIV NOTTINGHAM HOSP,QUEENS MED CTR,DEPT CLIN LAB SCI,DIV CLIN CHEM,NOTTINGHAM NG7 2UH,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1006/bbrc.1996.0544
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
Der p1, a cysteine proteinase derived from the house dust mite (HDM) Dermatophagoides pteronyssinus, is a major component of the allergic immune response in HDM atopic individuals. Recent evidence suggests that cysteine proteinase activity is important in the disease process as it increases the permeability of the allergen in the respiratory tract and disrupts the regulation of IgE synthesis. Der p1 is found in high concentrations in the faecal pellets of mites which are aerosolised and inhaled via the respiratory tract. The serine proteinase inhibitor, alpha(1)-antitrypsin, protects the lower respiratory tract against damage by proteinases released in the lung during inflammation. Der p1 catalytically inactivates alpha(1)-antitrypsin by a thiol-dependent mechanism involving specific cleavage of the reactive centre loop and we propose that this mechanism may be important in the pathogenesis of asthma. (C) 1996 Academic Press. Inc.
引用
收藏
页码:59 / 61
页数:3
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