TY - JOUR
T1 - Laminin expression by glial fibrillary acidic protein positive cells in human gliomas
AU - Tysnes, Berit BØlge
AU - Mahesparan, Rupavathana
AU - Thorsen, Frits
AU - Haugland, Hans Kristian
AU - Porwol, Torsten
AU - Enger, Per Øyvind
AU - Lund-Johansen, Morten
AU - Bjerkvig, Rolf
N1 - Funding Information:
This work was supported by the Norwegian Cancer Society, Familien Brynildsens Legat, Frank Mohn A/S, Inger Margrethe and Per Jæger and The Norwegian Research Council. The technical assistance of Tove Johansen, Bodil Hansen and Olav Bjørkelund is greatly appreciated.
PY - 1999/8
Y1 - 1999/8
N2 - Extracellular matrix components are regarded as important substrates for invasive tumor cells. The present work focuses on the expression of laminin in the brain in response to invading brain tumors. Biopsies obtained from tissue macroscopically evaluated as the border zone between tumor and normal brain, in 5 patients undergoing surgery for glioblastoma multiforme, were examined by immunocytochemistry and scanning confocal microscopy for the expression of laminin and glial fibrillary acidic protein. Laminin was mainly found in all the specimens associated with the basal lamina of blood vessels, but a variable degree of punctate laminin deposits were also observed in the parenchyma not associated with blood vessels. In the specimens with substantial deposits, scanning confocal microscopy showed that some of the laminin co-localized with intracellular glial fibrillary acidic protein.Punctate deposits of laminin were also seen in an intracranial BT4C rat glioma model, where it was particularly abundant in the brain/tumor confrontation zone. Previous in vitro studies have shown that laminin, among several extracellular matrix components, represent a highly permissive substrate for glioma cell migration. The presented results indicate that laminin can be produced by glial fibrillary acidic protein positive cells during glioma cell invasion in humans. This glycoprotein may thus represent one important substrate among many, which contribute to the invasive phenotype of gliomas. Copyright (C) 1999 ISDN.
AB - Extracellular matrix components are regarded as important substrates for invasive tumor cells. The present work focuses on the expression of laminin in the brain in response to invading brain tumors. Biopsies obtained from tissue macroscopically evaluated as the border zone between tumor and normal brain, in 5 patients undergoing surgery for glioblastoma multiforme, were examined by immunocytochemistry and scanning confocal microscopy for the expression of laminin and glial fibrillary acidic protein. Laminin was mainly found in all the specimens associated with the basal lamina of blood vessels, but a variable degree of punctate laminin deposits were also observed in the parenchyma not associated with blood vessels. In the specimens with substantial deposits, scanning confocal microscopy showed that some of the laminin co-localized with intracellular glial fibrillary acidic protein.Punctate deposits of laminin were also seen in an intracranial BT4C rat glioma model, where it was particularly abundant in the brain/tumor confrontation zone. Previous in vitro studies have shown that laminin, among several extracellular matrix components, represent a highly permissive substrate for glioma cell migration. The presented results indicate that laminin can be produced by glial fibrillary acidic protein positive cells during glioma cell invasion in humans. This glycoprotein may thus represent one important substrate among many, which contribute to the invasive phenotype of gliomas. Copyright (C) 1999 ISDN.
KW - Glial fibrillary acidic protein
KW - Glioblastoma
KW - Invasion
KW - Laminin
UR - http://www.scopus.com/inward/record.url?scp=0032824452&partnerID=8YFLogxK
U2 - 10.1016/S0736-5748(99)00055-6
DO - 10.1016/S0736-5748(99)00055-6
M3 - Article
C2 - 10571414
AN - SCOPUS:0032824452
SN - 0736-5748
VL - 17
SP - 531
EP - 539
JO - International Journal of Developmental Neuroscience
JF - International Journal of Developmental Neuroscience
IS - 5-6
ER -