Cortical spreading depression (CSD) develops during experimental stroke and within normal and traumatically injured human brain. Recently, (MMP) have been implicated in stroke pathogenesis and in the integrity of the neurovascular unit by degrading matrix proteins, enhancing blood brain barrier (BBB) permeability and brain edema, and promoting hemorrhage after tPA administration. Although brain injury or vascular mechanisms provide triggers, we recently found that intense neuronal glial depolarization during CSD activated MMP-9 for at least 72 hrs. and promotes perivascular plasma protein leakage. We propose 4 Aims to explore the novel hypothesis that MMP activation during CSD is caused in part by neuronal and glial activation directly and contributes to the development of edema in ischemia and BBB disruption in normal brain.
Aim 1 will confirm and extend preliminary data establishing CSD as a trigger for MMP activation and will identify relevant isoforms and cells of origin.
Aim 2 will test the hypothesis that CSD is accompanied by leakage of plasma protein caused by MMP activation and will extend preliminary data showing that, (1) permeability of Evans blue increases within ipsilateral vessels and that, (2) antigenicity of endothelial barrier antigen and laminin is decreased by MMP-dependent mechanisms after CSD.
Aim 3 will examine upstream mechanisms triggering MMP activation during CSD. Because nitric oxide s-nitrosylates the MMP active site to promote activation, we will examine whether CSD-induced NO generation triggers MMP activation and if so, examine the relevant NOS isoform promoting MMP activation by using selective NOS knockout mice. We will also examine the importance of NFkB and other pathways in the transcriptional regulation of MMP-9.
Aim 4 will examine the consequences of CSD-induced MMP activation during ischemia and explore the contributions of MMPs to vascular permeability changes both within the ischemic lesion and in remote brain areas. Using mutant mice lacking MMP-8 expressed on leucocytes, we propose to determine the extent to which MMP-8 causes MMP-induced BBB disruption in ischemic and non-ischemic tissue, and examine the potential for CSD-induced MMP-9 activation by MMP-8 dependent mechanisms in leucocytes. By doing so, we intend to explore ways in which neuronal activity during cerebral ischemia modulates the extracellular matrix and neurovascular unit and contribute to tissue injury.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS048198-02
Application #
6930314
Study Section
Special Emphasis Panel (ZRG1-CDIN (01))
Program Officer
Golanov, Eugene V
Project Start
2004-08-01
Project End
2009-05-31
Budget Start
2005-06-01
Budget End
2006-05-31
Support Year
2
Fiscal Year
2005
Total Cost
$171,500
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
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Qiu, Jianhua; Nishimura, Masaki; Wang, Yumei et al. (2008) Early release of HMGB-1 from neurons after the onset of brain ischemia. J Cereb Blood Flow Metab 28:927-38