Kramer B M, Van der Zee C E, Hagg T
Department of Anatomy and Neurobiology, Dalhousie University, Halifax, Nova Scotia, Canada.
Neuroscience. 1999;94(4):1163-72. doi: 10.1016/s0306-4522(99)00387-5.
The role of the p75 nerve growth factor receptor in the retrograde transport of neurotrophins in the adult CNS was investigated by comparing the transport of 125I-labeled neurotrophins by normal and p75 nerve growth factor receptor-deficient cholinergic septohippocampal neurons. In control mice, nerve growth factor was selectively transported from the hippocampal formation to the cholinergic neurons in the septum. Nerve growth factor labeling was found in three to four times as many septal cholinergic neuronal cell bodies than labeling for neurotrophin-3 or neurotrophin-4/5, and transported brain-derived neurotrophic factor was barely detectable. Cells were considered as labeled when the number of grains per cell exceeded five times background. In p75 nerve growth factor receptor-deficient mice, the number of cholinergic neurons labeled with each of the neurotrophins was reduced by 85-95%. Retrograde labeling of septohippocampal neurons with Fluorogold was not obviously reduced in p75 nerve growth factor receptor-deficient mice, suggesting that general transport mechanisms were not impaired. Despite the reduced neurotrophin transport, cholinergic neurons of p75 nerve growth factor receptor-deficient mice were larger than controls and had an apparently normal density of immunostaining for choline acetyltransferase. Since nerve growth factor is reportedly involved in size regulation and choline acetyltransferase expression, this raises the possibility that the retrograde transport itself is not essential for these events. Thus, p75 nerve growth factor receptor plays an important, although not exclusive, role in the transport of neurotrophins by cholinergic basal forebrain neurons, and retrograde transport of nerve growth factor may not be needed for regulating certain cellular processes.
通过比较正常和缺乏p75神经生长因子受体的胆碱能隔海马神经元对125I标记的神经营养因子的转运,研究了p75神经生长因子受体在成体中枢神经系统神经营养因子逆行转运中的作用。在对照小鼠中,神经生长因子从海马结构选择性转运至隔区的胆碱能神经元。在隔区胆碱能神经元胞体中发现的神经生长因子标记数量是神经营养因子-3或神经营养因子-4/5标记数量的三到四倍,而转运的脑源性神经营养因子几乎检测不到。当每个细胞的颗粒数超过背景值五倍时,细胞被视为有标记。在缺乏p75神经生长因子受体的小鼠中,用每种神经营养因子标记的胆碱能神经元数量减少了85 - 95%。在缺乏p75神经生长因子受体的小鼠中,用荧光金对隔海马神经元进行的逆行标记没有明显减少,这表明一般转运机制未受损。尽管神经营养因子转运减少,但缺乏p75神经生长因子受体的小鼠的胆碱能神经元比对照组大,并且胆碱乙酰转移酶免疫染色密度明显正常。由于据报道神经生长因子参与大小调节和胆碱乙酰转移酶表达,这增加了逆行转运本身对这些事件并非必不可少的可能性。因此,p75神经生长因子受体在胆碱能基底前脑神经元转运神经营养因子中起重要作用,尽管不是唯一作用,并且调节某些细胞过程可能不需要神经生长因子的逆行转运。