Increased plasma levels of matrix metalloproteinase-9 in patients with Alzheimer's disease

被引:208
作者
Lorenzl, S
Albers, DS
Relkin, N
Ngyuen, T
Hilgenberg, SL
Chirichigno, J
Cudkowicz, ME
Beal, MF
机构
[1] Cornell Univ, Weill Med Coll, Dept Neurol & Neurosci, New York, NY 10021 USA
[2] Massachusetts Gen Hosp, Neurol Clin Trial Unit, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Dept Neurol, Boston, MA 02114 USA
关键词
Alzheimer's disease; Parkinson's disease; matrix metalloproteinases; amyotrophic lateral sclerosis; tissue inhibitors of metalloproteinases;
D O I
10.1016/S0197-0186(03)00004-4
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
Matrix metalloproteinases (MMPs) may play a role in the pathophysiology of Alzheimer's disease (AD). MMP-9 and tissue inhibitors of metalloproteinases (TIMPs) are elevated in postmortem brain tissue of AD patients. MMPs and TIMPs are found in neurons, microglia, vascular endothelial cells and leukocytes. The aim of this study was to determine whether circulating levels of MMP-2, MMP-9, TIMP-1 and TIMP-2 are elevated in the plasma of AD patients. We compared AD patients to age- and gender-matched controls as well as to Parkinson's disease (PD) and amyotrophic lateral sclerosis (ALS) patients. There was constitutive expression of gelatinase A (MMP-2), and gelatinase B (MMP-9), in all the samples as shown by zymographic analysis. Levels of MMP-9 were significantly (P = 0.003) elevated in the plasma of AD patients as compared to controls. Plasma levels of MMP-2, TIMP-1 and TIMP-2 were unchanged. There were no significant changes of MMP-2, MMP-9, TIMP-1 and TIMP-2 levels in PD and ALS samples. TIMP-1 and TIMP-2 were significantly correlated with MMP-9 in the AD patients. ApoE genotyping of plasma samples showed that levels of MMP-2, TIMP-1 and TIMP-2 and MMP-9 were not significantly different between the ApoE subgroups. These findings indicate that circulating levels of MMP-9 are increased in AD and may contribute to disease pathology. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:191 / 196
页数:6
相关论文
共 35 条
  • [1] Albers DS, 2000, J NEURAL TRANSM-SUPP, P133
  • [2] Effects of matrix metalloproteinase-9 gene knock-out on the proteolysis of blood-brain barrier and white matter components after cerebral ischemia
    Asahi, M
    Wang, XY
    Mori, T
    Sumii, T
    Jung, JC
    Moskowitz, MA
    Fini, ME
    Lo, EH
    [J]. JOURNAL OF NEUROSCIENCE, 2001, 21 (19) : 7724 - 7732
  • [3] Role for matrix metalloproteinase 9 after focal cerebral ischemia, effects of gene knockout and enzyme inhibition with BB-94
    Asahi, M
    Asahi, K
    Jung, JC
    del Zoppo, GJ
    Fini, ME
    Lo, EH
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2000, 20 (12) : 1681 - 1689
  • [4] Asahina M, 2001, CLIN NEUROPATHOL, V20, P60
  • [5] CHARACTERIZATION OF NEUTRAL PROTEINASES FROM ALZHEIMER-AFFECTED AND CONTROL BRAIN SPECIMENS - IDENTIFICATION OF CALCIUM-DEPENDENT METALLOPROTEINASES FROM THE HIPPOCAMPUS
    BACKSTROM, JR
    MILLER, CA
    TOKES, ZA
    [J]. JOURNAL OF NEUROCHEMISTRY, 1992, 58 (03) : 983 - 992
  • [6] Backstrom JR, 1996, J NEUROSCI, V16, P7910
  • [7] Matrix metalloproteinase-9 is elevated in serum of patients with amyotrophic lateral sclerosis
    Beuche, W
    Yushchenko, M
    Mäder, M
    Maliszewska, M
    Felgenhauer, K
    Weber, F
    [J]. NEUROREPORT, 2000, 11 (16) : 3419 - 3422
  • [8] Increased oxidative damage to DNA in ALS patients
    Bogdanov, M
    Brown, RH
    Matson, W
    Smart, R
    Hayden, D
    O'Donnell, H
    Beal, MF
    Cudkowicz, M
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2000, 29 (07) : 652 - 658
  • [9] Tissue inhibitors of metalloproteinases: evolution, structure and function
    Brew, K
    Dinakarpandian, D
    Nagase, H
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY, 2000, 1477 (1-2): : 267 - 283