Neural Protection and Regeneration Section, National Institute on Drug Abuse, IRP, NIH, Baltimore, MD 21201, USA.
Exp Neurol. 2010 Sep;225(1):104-13. doi: 10.1016/j.expneurol.2010.05.020. Epub 2010 Jun 2.
Mesencephalic astrocyte-derived neurotrophic factor (MANF) is a secreted protein which reduces endoplasmic reticulum (ER) stress and has neurotrophic effects on dopaminergic neurons. Intracortical delivery of recombinant MANF protein protects tissue from ischemic brain injury in vivo. In this study, we examined the protective effect of adeno-associated virus serotype 7 encoding MANF in a rodent model of stroke. An AAV vector containing human MANF cDNA (AAV-MANF) was constructed and verified for expression of MANF protein. AAV-MANF or an AAV control vector was administered into three sites in the cerebral cortex of adult rats. One week after the vector injections, the right middle cerebral artery (MCA) was ligated for 60min. Behavioral monitoring was conducted using body asymmetry analysis, neurological testing, and locomotor activity. Standard immunohistochemical and western blotting procedures were conducted to study MANF expression. Our data showed that AAV-induced MANF expression is redistributed in neurons and glia in cerebral cortex after ischemia. Pretreatment with AAV-MANF reduced the volume of cerebral infarction and facilitated behavioral recovery in stroke rats. In conclusion, our data suggest that intracortical delivery of AAV-MANF increases MANF protein production and reduces ischemic brain injury. Ischemia also caused redistribution of AAV-mediated MANF protein suggesting an injury-induced release.
中脑星形胶质细胞衍生的神经营养因子(MANF)是一种分泌蛋白,可减轻内质网(ER)应激,并对多巴胺能神经元具有神经营养作用。在体内,皮质内给予重组 MANF 蛋白可保护组织免受缺血性脑损伤。在这项研究中,我们在中风的啮齿动物模型中检查了编码 MANF 的腺相关病毒血清型 7 的保护作用。构建了包含人 MANF cDNA 的腺相关病毒载体(AAV-MANF),并验证了 MANF 蛋白的表达。AAV-MANF 或 AAV 对照载体被递送至成年大鼠大脑皮质的三个部位。载体注射后一周,结扎右侧大脑中动脉(MCA)60min。通过身体不对称分析、神经学测试和运动活动进行行为监测。进行标准免疫组织化学和 Western 印迹程序以研究 MANF 表达。我们的数据表明,AAV 诱导的 MANF 表达在缺血后在大脑皮质中的神经元和神经胶质中重新分布。AAV-MANF 的预处理减少了中风大鼠的脑梗死体积并促进了行为恢复。总之,我们的数据表明,皮质内给予 AAV-MANF 可增加 MANF 蛋白的产生并减少缺血性脑损伤。缺血还导致 AAV 介导的 MANF 蛋白的重新分布,提示损伤诱导的释放。