학술논문

PECAM-1 and gelatinase B coexist in vascular cuffs of multiple sclerosis lesions.
Document Type
Article
Source
Neuropathology & Applied Neurobiology. Feb2006, Vol. 32 Issue 1, p15-22. 8p. 4 Black and White Photographs, 4 Diagrams.
Subject
*MULTIPLE sclerosis
*IMMUNOHISTOCHEMISTRY
*EXTRACELLULAR matrix proteins
*BLOOD plasma
*BLOOD cells
*CELL communication
*NEUROLOGICAL disorders
*NEUROBIOLOGY
Language
ISSN
0305-1846
Abstract
In multiple sclerosis (MS), the matrix metalloprotease (MMP) gelatinase B/MMP-9 and platelet endothelial cell adhesion molecule (PECAM)-1 have both been implicated in trans-endothelial infiltration of leucocytes into the brain, but their functional connection has not yet been investigated. We investigated the expression of gelatinase B and PECAM-1 in post mortem brains of MS patients by immunohistochemistry. Because increased soluble PECAM-1 serum levels have been observed in MS patients, we also tested in vitro whether this could be due to cleavage of PECAM-1 by gelatinase B or matrilysin-1/MMP-7. Constitutive expression of PECAM-1 was found on brain endothelial cells, whilst in active MS lesions cell-bound PECAM-1 was highly up-regulated on foamy macrophages in perivascular infiltrates and co-localized with gelatinase B. However, human THP-1 monocyte-bound or soluble recombinant PECAM-1 were both resistant to proteolytic cleavage by gelatinase B or matrilysin-1 in vitro, as demonstrated by Western blot analysis and flow cytometry. These results suggest that PECAM-1 and gelatinase B may complement each other during the transmigration of the blood–brain barrier by mononuclear cells. [ABSTRACT FROM AUTHOR]