Blood-brain barrier disruption by stromelysin-1 facilitates neutrophil infiltration in neuroinflammation

被引:204
作者
Gurney, Kate J.
Estrada, Eduardo Y.
Rosenberg, Gary A.
机构
[1] Univ New Mexico, Hlth Sci Ctr, Dept Neurol, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Hlth Sci Ctr, Dept Neurosci, Albuquerque, NM 87131 USA
[3] Univ New Mexico, Hlth Sci Ctr, Dept Cell Biol & Physiol, Albuquerque, NM 87131 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.nbd.2006.02.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Blood-brain barrier (BBB) opening is mediated by matrix metalloproteinases (MMPs) in neuroinflammation. We tested the hypothesis that MMP-3 plays a role in BBB damage, using MMP-3 knockout (KO) mice and lipopolysaccharide (LPS)-induced opening of the BBB. We found less disruption of the BBB after intracerebral LPS injection in MMP-3 KO mice than in wild type (P < 0.0006). MMP-3 KO mice had less MMP-9 than WT mice but similar levels of activation. Moreover, MMP-9 mRNA levels were increased to a similar level in both the MMP3 KO and WT, suggesting both endogenous and exogenous sources. Unbiased stereology showed increased neutrophil counts in the brains of MMP-3 WT compared to KO mice. Degradation of tight junction proteins, claudin-5 and occludin, and the basal lamina protein, laminin-alpha 1, was less affected in the KO than in the WT. Our results provide the first in vivo evidence that MMP-3 attacks the basal lamina and tight junction proteins, opening the BBB, thereby facilitating neutrophil influx. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:87 / 96
页数:10
相关论文
共 29 条
[1]   THE ACUTE INFLAMMATORY RESPONSE TO LIPOPOLYSACCHARIDE IN CNS PARENCHYMA DIFFERS FROM THAT IN OTHER BODY-TISSUES [J].
ANDERSSON, PB ;
PERRY, VH ;
GORDON, S .
NEUROSCIENCE, 1992, 48 (01) :169-186
[2]   Effects of matrix metalloproteinase-9 gene knock-out on the proteolysis of blood-brain barrier and white matter components after cerebral ischemia [J].
Asahi, M ;
Wang, XY ;
Mori, T ;
Sumii, T ;
Jung, JC ;
Moskowitz, MA ;
Fini, ME ;
Lo, EH .
JOURNAL OF NEUROSCIENCE, 2001, 21 (19) :7724-7732
[3]   Loss of the tight junction proteins occludin and zonula occludens-1 from cerebral vascular endothelium during neutrophil-induced blood-brain barrier breakdown in vivo [J].
Bolton, SJ ;
Anthony, DC ;
Perry, VH .
NEUROSCIENCE, 1998, 86 (04) :1245-1257
[4]   Multiple roles for MMPs and TIMPs in cerebral ischemia [J].
Cunningham, LA ;
Wetzel, M ;
Rosenberg, GA .
GLIA, 2005, 50 (04) :329-339
[5]   Focal cerebral ischemia induces active proteases that degrade microvascular matrix [J].
Fukuda, S ;
Fini, CA ;
Mabuchi, T ;
Koziol, JA ;
Eggleston, LL ;
del Zoppo, GJ .
STROKE, 2004, 35 (04) :998-1004
[6]   Claudin-1 and -2: Novel integral membrane proteins localizing at tight junctions with no sequence similarity to occludin [J].
Furuse, M ;
Fujita, K ;
Hiiragi, T ;
Fujimoto, K ;
Tsukita, S .
JOURNAL OF CELL BIOLOGY, 1998, 141 (07) :1539-1550
[7]   Matrix metalloproteinases in early diabetic retinopathy and their role in alteration of the blood-retinal barrier [J].
Giebel, SJ ;
Menicucci, G ;
McGuire, PG ;
Das, A .
LABORATORY INVESTIGATION, 2005, 85 (05) :597-607
[8]   S-nitrosylation of matrix metalloproteinases: Signaling pathway to neuronal cell death [J].
Gu, ZZ ;
Kaul, M ;
Yan, BX ;
Kridel, SJ ;
Cui, JK ;
Strongin, A ;
Smith, JW ;
Liddington, RC ;
Lipton, SA .
SCIENCE, 2002, 297 (5584) :1186-1190
[9]   MICROVASCULAR BASAL LAMINA ANTIGENS DISAPPEAR DURING CEREBRAL-ISCHEMIA AND REPERFUSION [J].
HAMANN, GF ;
OKADA, Y ;
FITRIDGE, R ;
DELZOPPO, GJ .
STROKE, 1995, 26 (11) :2120-2126
[10]   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