Title: role of matrix metalloproteinase-9 in progression of tuberculous meningitis: a pilot study in patients at different stages of the disease

被引:18
作者
Majeed, S. [1 ]
Singh, P. [2 ]
Sharma, N. [3 ]
Sharma, S. [1 ]
机构
[1] Postgrad Inst Med Educ & Res, Dept Biochem, Chandigarh 160012, India
[2] Postgrad Inst Med Educ & Res, Dept Neurol, Chandigarh 160012, India
[3] Postgrad Inst Med Educ & Res, Dept Internal Med, Chandigarh 160012, India
关键词
Antitubercular drugs; Inflammation; Mycobacterium tuberculosis; Matrixmetalloproteinase-9; SB-3CT; Tissue inhibitor of metalloproteinase-1; Tuberculous meningitis; NERVOUS-SYSTEM TUBERCULOSIS; MYCOBACTERIUM-TUBERCULOSIS; MATRIX METALLOPROTEINASES; CEREBROSPINAL-FLUID; GELATINASE-A; MMP-9; MACROPHAGES; EXPRESSION; INHIBITOR; SECRETION;
D O I
10.1186/s12879-016-1953-9
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: TBM (Tuberculous meningitis) is severe form of tuberculosis causing death of one third of the affected individuals or leaving two-third of the survivors disabled. MMP-9 (Matrix metalloproteinase-9) is produced by the central nervous system in a variety of inflammatory conditions and has a role in the breakdown of extracellular matrix and blood-brain barrier. Methods: In this study, the levels of MMP-9 and its inhibitor, TIMP-1 (tissue inhibitor of metalloproteinases-1), were screened using zymography and reverse zymography in cerebrospinal fluid and serum of tuberculous meningitis patients at different stages of the disease. Further, role of MMP-9 as therapeutic target was studied in C6 glioma cells infected with Mycobacterium tuberculosis H37Rv. Cells were treated with dexamethasone or SB-3CT (specific inhibitor of MMP-9) in combination with conventional antitubercular drugs. Results: MMP-9 levels in patients were increased as the disease progressed to advanced stages. The infection led to increased MMP-9 levels in C6 glioma cells and specific inhibition of MMP-9 by SB-3CT augmented bacillary clearance when used along with antitubercular drugs. Conclusion: MMP-9 plays a prominent role in progression of tuberculous meningitis from initial to advanced stages. Increased levels of MMP-9 during advancement of the disease leads to degeneration of nervous tissue and blood brain barrier disruption. Hence, MMP-9 can be considered as a therapeutic target for efficient management of TBM and can be explored to inhibit further progression of the disease if used at an early stage.
引用
收藏
页数:7
相关论文
共 25 条
[1]   Effect of Mycobacterium tuberculosis and its components on macrophages and the release of matrix metalloproteinases [J].
Chang, JC ;
Wysocki, A ;
TchouWong, KM ;
Moskowitz, N ;
Zhang, YH ;
Rom, WN .
THORAX, 1996, 51 (03) :306-311
[2]   Intracellular growth and drug susceptibility of Mycobacterium tuberculosis in macrophages [J].
Chanwong, Sakarin ;
Maneekarn, Niwat ;
Makonkawkeyoon, Luksana ;
Makonkawkeyoon, Sanit .
TUBERCULOSIS, 2007, 87 (02) :130-133
[3]   Inhibition of MMP-9 by a selective gelatinase inhibitor protects neurovasculature from embolic focal cerebral ischemia [J].
Cui, Jiankun ;
Chen, Shanyan ;
Zhang, Chunyang ;
Meng, Fanjun ;
Wu, Wei ;
Hu, Rong ;
Hadass, Or ;
Lehmidi, Tareq ;
Blair, Gregory J. ;
Lee, Mijoon ;
Chang, Mayland ;
Mobashery, Shahriar ;
Sun, Grace Y. ;
Gu, Zezong .
MOLECULAR NEURODEGENERATION, 2012, 7
[4]   Matrix metalloproteinases in tuberculosis [J].
Elkington, P. T. ;
Ugarte-Gil, C. A. ;
Friedland, J. S. .
EUROPEAN RESPIRATORY JOURNAL, 2011, 38 (02) :456-464
[5]  
Isabel BE, 2014, MALAYS J MED SCI, V21, P4
[6]   Dexamethasone regulation of matrix metalloproteinase expression in CNS vascular endothelium [J].
Harkness, KA ;
Adamson, P ;
Sussman, JD ;
Davies-Jones, GAB ;
Greenwood, J ;
Woodroofe, MN .
BRAIN, 2000, 123 :698-709
[7]   Monocytes infected with Mycobacterium tuberculosis regulate MAP kinase-dependent astrocyte MMP-9 secretion [J].
Harris, James E. ;
Green, Justin A. ;
Elkington, Paul T. ;
Friedland, Jon S. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2007, 81 (02) :548-556
[8]   Monocyte-astrocyte networks regulate matrix metalloproteinase gene expression and secretion in central nervous system tuberculosis in vitro and in vivo [J].
Harris, James E. ;
Nuttall, Robert K. ;
Elkington, Paul T. ;
Green, Justin A. ;
Horncastle, Donna E. ;
Graeber, Manuel B. ;
Edwards, Dylan R. ;
Friedland, Jon S. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (02) :1199-1207
[9]   QUANTITATIVE ZYMOGRAPHY - DETECTION OF PICOGRAM QUANTITIES OF GELATINASES [J].
KLEINER, DE ;
STETLERSTEVENSON, WG .
ANALYTICAL BIOCHEMISTRY, 1994, 218 (02) :325-329
[10]   Tuberculous cerebrovascular disease: A review [J].
Lammie, G. Alistair ;
Hewlett, Richard H. ;
Schoeman, Johan F. ;
Donald, Peter R. .
JOURNAL OF INFECTION, 2009, 59 (03) :156-166