McLeod M, Hong M, Mukhida K, Sadi D, Ulalia R, Mendez I
Cell Restoration Laboratory, Brain Repair Centre, 12th floor, Department of Anatomy and Neurobiology and Surgery, Neurosurgery, Dalhousie University, Halifax, Nova Scotia, Canada B3H 1X5.
Eur J Neurosci. 2006 Jul;24(2):361-70. doi: 10.1111/j.1460-9568.2006.04919.x.
Low dopaminergic cell survival and suboptimal fiber reinnervation are likely major contributing factors for the limited benefits of neural transplantation in Parkinson's disease (PD) patients. Glial cell lined-derived neurotrophic factor (GDNF) has been shown to enhance dopaminergic cell survival and fiber outgrowth of the graft site as well as promote behavioral recovery in rodent models of PD, while erythropoietin (EPO) can produce dopaminergic neuroprotective effects against 6-hydroxydopamine (6-OHDA) exposure on cultured neurons and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-treated mice. The aim of this study was to determine if fetal ventral mesencephalic (FVM) tissue exposed to hibernation media containing a combination of GDNF and EPO could enhance dopaminergic graft survival, striatal reinnervation and functional recovery in a 6-OHDA rodent model of PD. FVM tissue was dissected from 14-day-old rat fetuses and placed for 6 days in hibernation media alone, and in hibernation media that received either a daily administration of GDNF, EPO or a combination of GDNF and EPO. Following hibernation, FVM cells were transplanted as a single cell suspension into the striatum of unilateral 6-OHDA-lesioned rats. Rotational behavioral assessment revealed animals that received FVM tissue exposed to GDNF, EPO or the combination of both drugs had accelerated functional recovery. Immunohistochemical and stereological assessment revealed a significant increase in graft fiber density and angiogenesis into the graft when compared with control. These findings suggest that the hibernation of FVM tissue in a combination of GDNF and EPO can enhance graft efficacy and may have important implications for tissue preparation protocols for clinical neural transplantation in PD.
多巴胺能细胞存活率低和纤维再支配不理想可能是帕金森病(PD)患者神经移植获益有限的主要因素。胶质细胞源性神经营养因子(GDNF)已被证明可提高多巴胺能细胞存活率和移植部位的纤维生长,并促进PD啮齿动物模型的行为恢复,而促红细胞生成素(EPO)可对培养的神经元和1-甲基-4-苯基-1,2,3,6-四氢吡啶处理的小鼠产生针对6-羟基多巴胺(6-OHDA)暴露的多巴胺能神经保护作用。本研究的目的是确定暴露于含有GDNF和EPO组合的冬眠培养基中的胎儿腹侧中脑(FVM)组织是否能增强6-OHDA啮齿动物PD模型中的多巴胺能移植存活率、纹状体再支配和功能恢复。从14日龄大鼠胎儿中解剖出FVM组织,并将其单独置于冬眠培养基中,以及置于每天接受GDNF、EPO或GDNF与EPO组合的冬眠培养基中6天。冬眠后,将FVM细胞作为单细胞悬液移植到单侧6-OHDA损伤大鼠的纹状体中。旋转行为评估显示,接受暴露于GDNF、EPO或两种药物组合的FVM组织的动物功能恢复加快。免疫组织化学和立体学评估显示,与对照组相比,移植纤维密度和移植部位的血管生成显著增加。这些发现表明,GDNF和EPO组合对FVM组织进行冬眠可提高移植效果,可能对PD临床神经移植的组织制备方案具有重要意义。