Angiogenic proteins in brains of patients who died with cerebral malaria

被引:41
|
作者
Deininger, MH
Winkler, S
Kremsner, PG
Meyermann, R
Schluesener, HJ
机构
[1] Univ Tubingen, Sch Med, Inst Brain Res, D-72076 Tubingen, Germany
[2] Univ Vienna, Div Infect Dis, Dept Internal Med 1, Vienna, Austria
[3] Univ Tubingen, Sch Med, Inst Trop Med, Dept Parasitol, Tubingen, Germany
关键词
cerebral malaria; angiogenic remodeling; patients;
D O I
10.1016/S0165-5728(03)00250-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In cerebral malaria (CM), microvascular activation accompanies blood-brain barrier dysfunction which in turn represents the pathophysiological basis of neurological impairments in affected patients. To dissect the molecular basis of this process, we analyzed localization of proangiogenic vascular endothelial growth factor (VEGF), its receptor vascular endothelial growth factor receptor-1 (VEGFR-1, Flt-1), of downstream VEGF effectors matrix-metalloproteinase-1 (MMP-1) and connective tissue growth factor (CTGF), and of VEGF-interacting antiangiogenic thrombospondin-1 and -independent angiostatin in brains of patients who died with CM and controls by immunohistochemistry and Western blotting experiments. Most prominently, we detected more VEGF(+) astrocytes in CM patients and deposition of Flt-1 in Durck's granulomas. MMP-1 and thrombospondin-1 accumulated in macrophages/microglial cells in Durck's granulomas. In one CM patient, massive amounts of CTGF were detected as perivascular paracellular deposits. Angiostatin was observed in the serum of 2/7 control but in no CM patients. These data demonstrate the activation of the proangiogenic VEGF signaling cascade in patients with CM, probably reflecting compensatory mechanisms of general and focal brain hypoxia observed in these patients. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:101 / 111
页数:11
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