Mufson E J, Kroin J S, Sobreviela T, Burke M A, Kordower J H, Penn R D, Miller J A
Department of Neurological Sciences, Rush Presbyterian-St. Luke's Medical Center, Chicago, Illinois 60612.
Exp Neurol. 1994 Sep;129(1):15-26. doi: 10.1006/exnr.1994.1143.
The pattern of retrogradely transported BDNF, a member of the nerve growth family of neurotrophins, following intrastriatal infusion was immunohistochemically visualized within the rodent central nervous system. Human recombinant BDNF was infused at a rate of 3 micrograms/h for 7 days with an Alzet 2002 minipump prior to sacrifice. Tissue immunohistochemically processed using a turkey anti-BDNF antibody revealed retrogradely transported BNDF within neurons located mainly within the ipsilateral frontoparietal cortex (predominantly layer V), parafascicular and posterior thalamic nuclei, and substantia nigra, pars compacta. Sections dual immunoreacted for BNNF and tyrosine hydroxylase revealed a subpopulation of dopaminergic neurons (approximately 28%) within the pars compacta which contained retrogradely transported BDNF. Experiments in which a mixture of BDNF and the retrograde tracer fluorogold were simultaneously infused for 7 days into the striatum revealed BDNF and fluorogold single-labeled neurons as well as BDNF and fluorogold dual-labeled cells within the substantia nigra, pars compacta. These observations indicate that only a subpopulation of neurons within the substantia nigra retrogradely transport BDNF following intrastriatal infusion and thus only a subpopulation of cells may be responsive to the trophic influences of BDNF. The retrograde transport of trophins, such as BDNF, represents a unique neuroanatomical tool to selectivity map the location of specific neurotrophin-responsive systems. Unraveling the trophic anatomy of BDNF will aid in understanding its role in development, degeneration, and experimental animal models of regeneration providing essential data for its use in clinical neurodegenerative disorders including Parkinson's disease.
在啮齿动物中枢神经系统内,通过免疫组织化学方法观察了神经营养因子神经生长因子家族成员脑源性神经营养因子(BDNF)在纹状体内注射后逆行运输的模式。在处死前,使用Alzet 2002微型泵以3微克/小时的速率注入人重组BDNF,持续7天。使用火鸡抗BDNF抗体进行免疫组织化学处理的组织显示,逆行运输的BDNF主要存在于同侧额顶叶皮质(主要是V层)、束旁核和丘脑后核以及黑质致密部的神经元内。对BDNF和酪氨酸羟化酶进行双重免疫反应的切片显示,致密部内约28%的多巴胺能神经元亚群含有逆行运输的BDNF。将BDNF和逆行示踪剂荧光金的混合物同时注入纹状体7天的实验显示,黑质致密部内有BDNF单标记神经元、荧光金单标记神经元以及BDNF和荧光金双标记细胞。这些观察结果表明,纹状体内注射后,黑质内只有一部分神经元逆行运输BDNF,因此只有一部分细胞可能对BDNF的营养作用有反应。BDNF等神经营养因子的逆行运输是一种独特的神经解剖学工具,可用于选择性绘制特定神经营养因子反应系统的位置。阐明BDNF的营养解剖学将有助于理解其在发育、退化以及再生实验动物模型中的作用,为其在包括帕金森病在内的临床神经退行性疾病中的应用提供重要数据。