(Stroke. 1997;28:858-865.)
© 1997 American Heart Association, Inc.
Articles |
6ß4 During Focal Cerebral Ischemia/Reperfusion
From the Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, Calif.
Correspondence to Gregory J. del Zoppo, MD, Department of Molecular and Experimental Medicine, The Scripps Research Institute, 10550 N Torrey Pines Rd, SBR-17, La Jolla, CA 92037. E-mail GRGDLZOP{at}RISCSM.SCRIPPS.EDU
Background and Purpose Integrins participate in cerebral
microvascular integrity and signaling during focal
ischemia/reperfusion. The integrin subunits
1,
6, and ß1 are distributed identically on
normal cerebral microvessels. Studies in epithelium indicate that
integrin
6ß4, which interacts with
laminin-5 in the basal lamina/extracellular matrix, is unique. This
study describes the exact location of
6,
ß4, and
6ß4 and that their
responses in focal cerebral ischemia are relevant to
astrocyte-matrix interactions.
Methods The effect of middle cerebral artery occlusion and
subsequent reperfusion on the microvascular expression of
6ß4 and laminin-5 in regions of cellular
injury (dUTP incorporation) was examined in 15 nonhuman primates.
Well-characterized antibodies against human
6,
ß4,
6ß4, laminin-5 and
laminin-1, endothelial CD31, and vascular markers were
measured with computerized video imaging and laser confocal
microscopy.
Results Integrin
6ß4 was
localized on astrocytes where it connects with the extracellular matrix
at the astrocyte-vessel interface. It represented
59.3±16.4% of
6 antigen in cerebral microvessels
<100 µm in diameter. By 2 hours of ischemia, the
significant reduction in
6 expression
(2P<.001) was accompanied by decreases in
ß4/laminin-5 (0.76±0.03 to 0.20±0.09;
2P=.001) and
6ß4/laminin-5
(0.73±0.18 to 0.25±0.11; 2P=.001) in the region of dUTP
incorporation. Parallel changes in laminin-5 and laminin-1 were less
pronounced and coincided by 24 hours.
Conclusions This is the first description of a potential
role of integrin
6ß4 in the brain, where
it mediates astrocyte-matrix interactions. The dramatic disappearance
of
6ß4 relative to its ligands reflects
early loss of integrity between the astrocyte and the vessel wall in
selected microvessels in response to ischemia.
Key Words: astrocytes cell adhesion molecules cerebral ischemia microvascular injury baboons
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