Effect of VEGF and its receptor antagonist SU-5416, an inhibitor of angiogenesis, on processing of the β-amyloid precursor protein in primary neuronal cells derived from brain tissue of Tg2576 mice

被引:20
作者
Buerger, Susanne
Yafai, Yousef [2 ]
Bigl, Marina [3 ]
Wiedemann, Peter [2 ]
Schliebs, Reinhard [1 ]
机构
[1] Univ Leipzig, Paul Flechsig Inst Brain Res, Dept Neurochem, Fac Med, D-04109 Leipzig, Germany
[2] Univ Leipzig, Univ Hosp, Dept Eye Clin, D-04109 Leipzig, Germany
[3] Univ Leipzig, Fac Med, Inst Biochem, D-04109 Leipzig, Germany
关键词
Amyloid beta; ELISA; alpha-Secretase; beta-Secretase; Primary neuron-rich cell culture; Tg2576; mouse; VEGF receptor; RT-PCR; Neuronal VEGF secretion; ENDOTHELIAL GROWTH-FACTOR; TRANSGENIC MOUSE MODEL; ALZHEIMERS-DISEASE; CEREBRAL MICROVASCULATURE; HYPOXIA; ANGIOPATHY; DEPOSITION; ISCHEMIA; VESSELS; BARRIER;
D O I
10.1016/j.ijdevneu.2010.07.231
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
A large number of Alzheimer patients demonstrate cerebrovascular pathology, which has been assumed to be related to beta-amyloid (A beta) deposition. A beta peptides have been described to inhibit angiogenesis both in vitro and in vivo, and deregulation of angiogenic factors may contribute to various neurological disorders including neurodegeneration. One of the key angiogenic factor is the vascular endothelial growth factor (VEGF). Increased levels of VEGF have been observed in brains of Alzheimer patients, while the functional significance of VEGF up-regulation in the pathogenesis and progression of AD is still a matter of debate. To test whether VEGF may affect neuronal APP processing, primary neuronal cells derived from brain tissue of El 6 embryos of Tg2576 mice were exposed with 1 ng/ml VEGF for 6, 12, and 24 h, followed by monitoring formation and secretion of soluble A beta peptides, release of the human APP cleavage products, sAPP beta swe and sAPP alpha, into the culture medium as well as the activities of alpha- and beta-secretases in neuronal cell extracts. Exposure of primary neuronal cells by VEGF for 24 h led to slightly reduced sAPP beta release, accompanied by decreased beta-secretase activity 12 h after VEGF exposure. Incubation of neurons by the VEGF receptor antagonist and angiogenesis inhibitor SU-5416 for 24h resulted in increased release of sAPP beta swe, and strikingly enhanced secretion of A beta peptides into the culture medium, which was accompanied by a significant increase in beta-secretase activity, as compared to control incubations. The SU-5416-induced effects on APP processing could not be suppressed by the additional presence of VEGF, suggesting that SU-5416 affects pathways that are apparently independent of VEGF receptor signaling. The data obtained indicate that VEGF-driven mechanisms may affect APP processing, suggesting a link of angiogenesis and pathogenesis of Alzheimer's disease. (C) 2010 ISDN. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:597 / 604
页数:8
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