Studer L, Spenger C, Seiler R W, Altar C A, Lindsay R M, Hyman C
Department of Neurosurgery, University of Bern, Inselspital, Switzerland.
Eur J Neurosci. 1995 Feb 1;7(2):223-33. doi: 10.1111/j.1460-9568.1995.tb01058.x.
The effect of the various neurotrophin family members on the morphological structure of dopaminergic neurons was compared in dissociated cultures of embryonic rat ventral mesencephalon. Cultures were maintained in vitro in the presence of brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), neurotrohin-4/5 (NT-4/5), nerve growth factor (NGF) or no added growth factors. Three-dimensional reconstructions of 48 neurons were made in each of the experimental groups following immunocytochemical staining for tyrosine hydroxylase to detect dopaminergic neurons. In addition [3H]mazindol binding analyses were carried out in replicate cultures in order to quantify the effects of the neurotrophins on the number of dopamine uptake sites. Among the neurotrophins tested, NT-4/5 influenced the proximal morphological parameters most, as determined by a 36% increase in the soma profile area and 35% in the number of stem neurites. Analysis of neuritic size and complexity in these cultures revealed that combined neuritic length and number of segments/cell were increased by 45 and 40% respectively. A change in neurite complexity in the NT-4/5 treated cultures was further confirmed using Scholl's concentric sphere analysis. In addition, relative to the control, NT-4/5 increased the neuronal differentiation as evidenced by increases in varicosity density and [3H]mazindol binding by 114 and 101% respectively. BDNF and, to a lesser extent, NT-3 also increased both proximal parameters and parameters of differentiation, but were without effect on parameters of neuritic size and complexity. No effects on neuronal structure were observed in NGF treated cultures. These findings demonstrate that BDNF, NT-3 and NT-4/5 influence the morphological differentiation of dopaminergic neurons in vitro, suggesting they may play a role in the structural development and plasticity of these neurons in the mesencephalon.
在胚胎大鼠腹侧中脑的解离培养物中,比较了各种神经营养因子家族成员对多巴胺能神经元形态结构的影响。培养物在体外分别添加脑源性神经营养因子(BDNF)、神经营养因子-3(NT-3)、神经营养因子-4/5(NT-4/5)、神经生长因子(NGF)或不添加生长因子的条件下维持培养。对每个实验组中48个神经元进行免疫细胞化学染色以检测酪氨酸羟化酶,从而进行多巴胺能神经元的三维重建。此外,在重复培养物中进行[3H]马吲哚结合分析,以量化神经营养因子对多巴胺摄取位点数量的影响。在所测试的神经营养因子中,NT-4/5对近端形态学参数影响最大,其表现为胞体轮廓面积增加36%,主干神经突数量增加35%。对这些培养物中神经突大小和复杂性的分析表明,神经突总长度和每个细胞的节段数分别增加了45%和40%。使用肖尔同心球分析法进一步证实了NT-4/5处理的培养物中神经突复杂性的变化。此外,相对于对照组,NT-4/5使神经元分化增加,表现为曲张密度增加114%,[3H]马吲哚结合增加101%。BDNF以及在较小程度上NT-3也增加了近端参数和分化参数,但对神经突大小和复杂性参数没有影响。在NGF处理的培养物中未观察到对神经元结构的影响。这些发现表明,BDNF、NT-3和NT-4/5在体外影响多巴胺能神经元的形态分化,表明它们可能在中脑这些神经元的结构发育和可塑性中发挥作用。