Journal of Southern Medical University ›› 2006, Vol. 26 ›› Issue (10): 1388-1393.

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Protective effect of adeno-associated viral vector-mediated expression of human brain-derived neurotrophic factor in rat neurons against beta-amyloid-induced Alzheimer’s disease in vitro

LIU Zhao-hui, MA Dong-liang, JIN Hui, MA Yan-bing, HU Hai-tao Department of Anatomy and Histology-Embryology, Key Laboratory of Environment and Genes Related of Disease, Ministry of Education, School of Medicine, Xi’an Jiaotong University, Xi’an 710061, China   

  1. 西安交通大学医学院解剖与组织胚胎学系环境与基因相关疾病教育部重点实验室; 西安交通大学医学院解剖与组织胚胎学系环境与基因相关疾病教育部重点实验室 陕西西安710061; 陕西西安710061;
  • Online:2006-10-20 Published:2006-10-20

Abstract: Objective To achieve expression of human brain-derived neurotrophic factor (hBDNF) mediated by recombinant adeno-associated virus (rAAV) and explore the mechanism of its neuroprotective effects in rat neurons against beta-amyloid-induced Alzheimer’s disease. Methods Using molecular cloning technique, rAAV vector containing hBDNF gene (AAV-hBDNF) was constructed to transfect SD rat hippocampal neurons exposed to beta-amyloid treatment. The changes in cell apoptosis were observed by MTT assay and flow cytometry, and the expression of hBDNF and Bcl-2 protein were determined by immunocytochemical staining. Laser scanning confocal microscopy (LSCM) was used to observe the changes of [Ca2+]i. Results The cultured rat hippocampal neurons were effectively transfected with AAV-hBDNF and expression of BDNF protein was obviously increased. hBNDF expression showed significant protective effects against beta-amyloid-induced neuronal damage, and the expression of Bcl-2 protein was increased significantly and the balance of [Ca2+]i was maintained in BDNF-treated cells with beta-amyloid exposure. Conclusion hBDNF expression can effectively protect cultured rat hippocampal cells from beta-amyloid-induced apoptosis through inhibiting the intracellular calcium overload and increasing the expression of Bcl-2 protein. 

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