Center for Neuropsychiatric Research, National Health Research Institute, Zhunan, Taiwan ; Neural Protection and Regeneration Section, National Institute on Drug Abuse, Intramural Research Program, Baltimore, Maryland, United States of America.
PLoS One. 2013 Dec 2;8(12):e81750. doi: 10.1371/journal.pone.0081750. eCollection 2013.
Migration of new neuroprogenitor cells (NPCs) from the subventricular zone (SVZ) plays an important role in neurorepair after injury. Previous studies have shown that brain derived neurotrophic factor (BDNF) enhances the migration of NPCs from SVZ explants in neonatal mice in vitro. The purpose of this study was to identify the role of BDNF in SVZ cells using AAV-BDNF in an animal model of stroke. BDNF protein production after AAV-BDNF infection was verified in primary neuronal culture. AAV-BDNF or AAV-RFP was injected into the left SVZ region of adult rats at 14 days prior to right middle cerebral artery occlusion (MCAo). SVZ tissues were collected from the brain and placed in Metrigel cultures 1 day after MCAo. Treatment with AAV-BDNF significantly increased the migration of SVZ cells in the stroke brain in vitro. In another set of animals, AAV-GFP was co-injected with AAV-BDNF or AAV-RFP to label cells in left SVZ prior to right MCAo. Local administration of AAV-BDNF significantly enhanced recovery of locomotor function and migration of GFP-positive cells from the SVZ toward the lesioned hemisphere in stroke rats. Our data suggest that focal administration of AAV-BDNF to the SVZ increases behavioral recovery post stroke, possibly through the enhancement of migration of cells from SVZ in stroke animals. Regional manipulation of BDNF expression through AAV may be a novel approach for neurorepair in stroke brains.
新的神经祖细胞(NPCs)从侧脑室下区(SVZ)迁移在损伤后神经修复中起着重要作用。先前的研究表明,脑源性神经营养因子(BDNF)增强了新生小鼠 SVZ 外植体中 NPC 的迁移。本研究旨在使用 AAV-BDNF 在中风动物模型中确定 BDNF 在 SVZ 细胞中的作用。在原代神经元培养物中验证了 AAV-BDNF 感染后的 BDNF 蛋白产生。在右侧大脑中动脉闭塞(MCAo)前 14 天,将 AAV-BDNF 或 AAV-RFP 注射到成年大鼠的左侧 SVZ 区域。在 MCAo 后 1 天,从大脑中收集 SVZ 组织并置于 Metrigel 培养物中。在体外,用 AAV-BDNF 处理显着增加了中风脑 SVZ 细胞的迁移。在另一组动物中,在右侧 MCAo 前,将 AAV-GFP 与 AAV-BDNF 或 AAV-RFP 共注射到左侧 SVZ 以标记细胞。SVZ 中的细胞迁移到中风大鼠的损伤半球。我们的数据表明,向 SVZ 局部给予 AAV-BDNF 可增加中风后行为的恢复,这可能是通过增强中风动物 SVZ 中细胞的迁移来实现的。通过 AAV 对 BDNF 表达的区域操作可能是中风大脑神经修复的一种新方法。