Scatter factor hepatocyte growth factor gene transfer increases rat blood-glioma barrier permeability

被引:14
作者
Book, AA
Ranganathan, S
Abounader, R
Rosen, E
Laterra, J
机构
[1] Kennedy Krieger Res Inst, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21287 USA
[4] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21287 USA
[5] Long Isl Jewish Med Ctr, Albert Einstein Coll Med, Dept Radiat Oncol, New Hyde Park, NY 11042 USA
关键词
blood-brain barrier; brain tumor; edema; glioma; horseradish peroxidase; vascular endothelial growth factor;
D O I
10.1016/S0006-8993(99)01527-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Malignant gliomas are associated with a dysfunctional blood-tumor barrier (BTB) that causes substantial morbidity, Scatter factor/hepatocyte growth factor (SF/HGF) is a multifunctional growth factor that correlates with glioma malignancy and has several biological properties that suggest a role in enhancing blood-glioma barrier permeability. In this study, we examined the effects of glioma cell SF/HGF expression on BTB permeability to horseradish peroxidase (HRP). Fischer 344 rats bearing intrastriatal 9L tumors engineered to secrete SF/HGF (9L-SF) and SF/HGF-negative control tumors (BL-neo) received intracardiac injections of HRP and were rapidly decapitated. Densitometric analysis of brain sections reacted with diaminobenzidine showed significantly greater extravascular HRP surrounding SF/HGF-secreting tumors than 9L-neo tumors of comparable size (p < 0.05). HRP enzymatic activity associated with striata containing SF/HGF-expressing tumors was 1.6-fold greater than that of striata containing control tumors (p < 0.05). Northern analysis showed that expression of vascular endothelial growth factor/vascular permeability factor (VEGF/VPF) did not differ between 9L-neo and 9L-SF tumors. These data demonstrate that SF/HGF expression by intracerebral glial tumors can enhance BTB permeability independent of changes in VEGF/VPF expression, (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:173 / 180
页数:8
相关论文
共 62 条
[1]  
Adachi T, 1996, HEPATOLOGY, V24, P1274
[2]   Neutral proteases and disruption of the blood-brain barrier in rat [J].
Armao, D ;
Kornfeld, M ;
Estrada, EY ;
Grossetete, M ;
Rosenberg, GA .
BRAIN RESEARCH, 1997, 767 (02) :259-264
[3]   DIFFERENTIAL EXPRESSION OF VASCULAR ENDOTHELIAL GROWTH-FACTOR (VASCULAR-PERMEABILITY FACTOR) FORMS IN RAT-TISSUES [J].
BACIC, M ;
EDWARDS, NA ;
MERRILL, MJ .
GROWTH FACTORS, 1995, 12 (01) :11-15
[4]   EXPRESSION OF THE VASCULAR-PERMEABILITY FACTOR VASCULAR ENDOTHELIAL GROWTH-FACTOR GENE IN CENTRAL-NERVOUS-SYSTEM NEOPLASMS [J].
BERKMAN, RA ;
MERRILL, MJ ;
REINHOLD, WC ;
MONACCI, WT ;
SAXENA, A ;
CLARK, WC ;
ROBERTSON, JT ;
ALI, IU ;
OLDFIELD, EH .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (01) :153-159
[5]  
BREM S, 1972, J NATL CANCER I, V48, P347
[6]  
BURGER PC, 1985, CANCER, V56, P1106, DOI 10.1002/1097-0142(19850901)56:5<1106::AID-CNCR2820560525>3.0.CO
[7]  
2-2
[8]   HEPATOCYTE GROWTH-FACTOR IS A POTENT ANGIOGENIC FACTOR WHICH STIMULATES ENDOTHELIAL-CELL MOTILITY AND GROWTH [J].
BUSSOLINO, F ;
DIRENZO, MF ;
ZICHE, M ;
BOCCHIETTO, E ;
OLIVERO, M ;
NALDINI, L ;
GAUDINO, G ;
TAMAGNONE, L ;
COFFER, A ;
COMOGLIO, PM .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :629-641
[9]   FURTHER CHARACTERIZATION OF MALIGNANT GLIOMA-DERIVED VASCULAR-PERMEABILITY FACTOR [J].
CRISCUOLO, GR ;
MERRILL, MJ ;
OLDFIELD, EH .
JOURNAL OF NEUROSURGERY, 1988, 69 (02) :254-262
[10]   THE FMS-LIKE TYROSINE KINASE, A RECEPTOR FOR VASCULAR ENDOTHELIAL GROWTH-FACTOR [J].
DEVRIES, C ;
ESCOBEDO, JA ;
UENO, H ;
HOUCK, K ;
FERRARA, N ;
WILLIAMS, LT .
SCIENCE, 1992, 255 (5047) :989-991