Filter sterilization of highly infectious samples to prevent false negative analysis of matrix metalloproteinase activity

被引:20
作者
Elkington, PTG [1 ]
Green, JA [1 ]
Friedland, JS [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Infect Dis, London W12 0NN, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
matrix metalloproteinases; infection; filtration;
D O I
10.1016/j.jim.2005.11.010
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Matrix metalloproteinases (MMPs) are implicated in the immunopathology of numerous infectious diseases. High risk samples such as those generated after infection with Mycobacterium tuberculosis require filter sterilization for safe analysis of MMP concentrations. Here, we report that commercial filter membranes may cause artefacts by binding MMPs. Anopore 0.2 mu M membrane filtration reduced MMP-1 concentrations to undetectable levels by zymography and Western blotting. Polypropylene 0.45 mu M filtration removed some MMP-1, while Polysulphone, Durapore and Bio-inert 0.2 mu M membranes did not remove MMP-1. Anopore filtration also removed all MMP-7 and -9 activity, suggesting that the conserved MMP catalytic domain binds the membrane. This study demonstrates the importance of selecting the appropriate filter in MMP analysis to avoid incorrectly excluding MMP involvement in infection-related immunopathology. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 119
页数:5
相关论文
共 10 条
[1]   PAR1 is a matrix metalloprotease-1 receptor that promotes invasion and tumorigenesis of breast cancer cells [J].
Boire, A ;
Covic, L ;
Agarwal, A ;
Jacques, S ;
Sherifl, S ;
Kuliopulos, A .
CELL, 2005, 120 (03) :303-313
[2]   PROPERTIES OF MICROFILTRATION MEMBRANES - MECHANISMS OF FLUX LOSS IN THE RECOVERY OF AN ENZYME [J].
BOWEN, WR ;
HALL, NJ .
BIOTECHNOLOGY AND BIOENGINEERING, 1995, 46 (01) :28-35
[3]   Mycobacterium tuberculosis, but not vaccine BCG, specifically upregulates matrix metalloproteinase-1 [J].
Elkington, PTG ;
Nuttall, RK ;
Boyle, JJ ;
O'Kane, CM ;
Horncastle, DE ;
Edwards, DR ;
Friedland, JS .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 172 (12) :1596-1604
[4]   Mycobacterium tuberculosis up-regulates matrix metalloproteinase-1 secretion from human airway epithelial cells via a p38 MAPK switch [J].
Elkington, PTG ;
Emerson, JE ;
Lopez-Pascua, LDC ;
O'Kane, CM ;
Horncastle, DE ;
Boyle, JJ ;
Friedland, JS .
JOURNAL OF IMMUNOLOGY, 2005, 175 (08) :5333-5340
[5]   Zymography: A single-step staining method for quantitation of proteolytic activity on substrate gels [J].
Leber, TM ;
Balkwill, FR .
ANALYTICAL BIOCHEMISTRY, 1997, 249 (01) :24-28
[6]   Regulation of matrix metalloproteinases and their inhibitor genes in lipopolysaccharide-induced endotoxemia in mice [J].
Pagenstecher, A ;
Stalder, AK ;
Kincaid, CL ;
Volk, B ;
Campbell, IL .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (01) :197-210
[7]   Matrix metalloproteinases as modulators of inflammation and innate immunity [J].
Parks, WC ;
Wilson, CL ;
López-Boado, YS .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (08) :617-629
[8]  
PITT A M, 1987, Journal of Parenteral Science and Technology, V41, P110
[9]   Zymographic techniques for the analysis of matrix metalloproteinases and their inhibitors [J].
Snoek-van Beurden, PAM ;
Von den Hoff, JW .
BIOTECHNIQUES, 2005, 38 (01) :73-83
[10]   HIV-induced metalloproteinase processing of the chemokine stromal cell derived factor-1 causes neurodegeneration [J].
Zhang, KY ;
McQuibban, GA ;
Silva, C ;
Butler, GS ;
Johnston, JB ;
Holden, J ;
Clark-Lewis, I ;
Overall, CM ;
Power, C .
NATURE NEUROSCIENCE, 2003, 6 (10) :1064-1071