Em. Cornford et al., HIGH EXPRESSION OF THE GLUT1 GLUCOSE-TRANSPORTER IN HUMAN BRAIN HEMANGIOBLASTOMA ENDOTHELIUM, Journal of neuropathology and experimental neurology, 54(6), 1995, pp. 842-851
The principal glucose transporter at the blood-brain barrier is Glut1,
and GLUT1 expression is downregulated in high grade gliomas. In the p
resent study, glucose transporter expression was studied in surgically
resected hemangioblastoma tissue. Light microscopic immunochemistry i
ndicated the high expression of the Glut1 glucose transporter isoform
throughout the central vascular endothelium of this tissue. Glial fibr
illary acidic protein (GFAP) was observed only at the tumor border, wi
th no GFAP immunoreactivity in stromal cells, pericytes or endothelia
in the central tumor regions. It is generally believed that more Glut1
is found in erythrocytes than any other cell, but quantitative electr
on microscopic immunogold analyses of Glut1-immunoreactive sites per m
icron of capillary membrane showed the Glut1 density in tumor endothel
ial membranes glucose transporter was 2-3-fold higher than in human re
d cells. In the same tissue samples, qualitative immunogold electron m
icroscopy of human serum albumin indicated that this protein (MW 65,00
0) moved freely from the vascular space into pericapillary regions, co
nfirming the leaky barrier characteristics of the hemangioblastoma. Th
ese studies show that Glut1 expression may be high in endothelia that
are highly permeable and devoid of astroglial contacts. Thus, human ce
rebral hemangioblastomas may provide a novel system for studying the i
nduction of Glut1 in the blood-brain barrier.