TY - JOUR
T1 - MMP-2/MMP-9 plasma level and brain expression in cerebral amyloid angiopathy-associated hemorrhagic stroke
AU - Hernandez-Guillamon, Mar
AU - Martinez-Saez, Elena
AU - Delgado, Pilar
AU - Domingues-Montanari, Sophie
AU - Boada, Cristina
AU - Penalba, Anna
AU - Boada, Mercè
AU - Pagola, Jorge
AU - Maisterra, Olga
AU - Rodriguez-Luna, David
AU - Molina, Carlos A.
AU - Rovira, Alex
AU - Alvarez-Sabin, José
AU - Ortega-Aznar, Arantxa
AU - Montaner, Joan
PY - 2012/3
Y1 - 2012/3
N2 - Cerebral amyloid angiopathy (CAA) is one of the main causes of intracerebral hemorrhage (ICH) in the elderly. Matrix metalloproteinases (MMPs) have been implicated in blood-brain barrier disruption and ICH pathogenesis. In this study, we determined the levels MMP-2 and MMP-9 in plasma and their brain expression in CAA-associated hemorrhagic stroke. Although MMP-2 and MMP-9 plasma levels did not differ among patients and controls, their brain expression was increased in perihematoma areas of CAA-related hemorrhagic strokes compared with contralateral areas and nonhemorrhagic brains. In addition, MMP-2 reactivity was found in β-amyloid (Aβ)-damaged vessels located far from the acute ICH and in chronic microbleeds. MMP-2 expression was associated to endothelial cells, histiocytes and reactive astrocytes, whereas MMP-9 expression was restricted to inflammatory cells. In summary, MMP-2 expression within and around Aβ-compromised vessels might contribute to the vasculature fatal fate, triggering an eventual bleeding.
AB - Cerebral amyloid angiopathy (CAA) is one of the main causes of intracerebral hemorrhage (ICH) in the elderly. Matrix metalloproteinases (MMPs) have been implicated in blood-brain barrier disruption and ICH pathogenesis. In this study, we determined the levels MMP-2 and MMP-9 in plasma and their brain expression in CAA-associated hemorrhagic stroke. Although MMP-2 and MMP-9 plasma levels did not differ among patients and controls, their brain expression was increased in perihematoma areas of CAA-related hemorrhagic strokes compared with contralateral areas and nonhemorrhagic brains. In addition, MMP-2 reactivity was found in β-amyloid (Aβ)-damaged vessels located far from the acute ICH and in chronic microbleeds. MMP-2 expression was associated to endothelial cells, histiocytes and reactive astrocytes, whereas MMP-9 expression was restricted to inflammatory cells. In summary, MMP-2 expression within and around Aβ-compromised vessels might contribute to the vasculature fatal fate, triggering an eventual bleeding.
KW - MMP-2
KW - MMP-9
KW - cerebral amyloid angiopathy
KW - hemorrhagic stroke
KW - intracerebral hemorrhage
KW - matrix metalloproteinase
UR - http://www.scopus.com/inward/record.url?scp=84857657375&partnerID=8YFLogxK
U2 - 10.1111/j.1750-3639.2011.00512.x
DO - 10.1111/j.1750-3639.2011.00512.x
M3 - Article
C2 - 21707819
AN - SCOPUS:84857657375
SN - 1015-6305
VL - 22
SP - 133
EP - 141
JO - Brain Pathology
JF - Brain Pathology
IS - 2
ER -