Spenger C, Hyman C, Studer L, Egli M, Evtouchenko L, Jackson C, Dahl-Jørgensen A, Lindsay R M, Seiler R W
Department of Neurosurgery, University of Bern, Switzerland.
Exp Neurol. 1995 May;133(1):50-63. doi: 10.1006/exnr.1995.1007.
The neurotrophin brain-derived neurotrophic factor (BDNF) was tested for its ability to promote the survival and regulation of expression of phenotypic markers of dopaminergic, serotonergic, and GABAergic neurons in free-floating roller tube cultures of human fetal ventral mesencephalon. This culture system contains neurons of the anlage of the substantia nigra as well as that of the rostral raphe nucleus. Dopaminergic neuron number and tyrosine hydroxylase (TH) fiber density was monitored by TH immunocytochemistry. Measurement of dopamine (DA) content, TH enzymatic activity, serotonin (5-HT) content, and glutamic acid decarboxylase (GAD) activity were used as indices of their respective neurotransmitter function. The presence of GABAergic and serotonergic neurons in this culture system was confirmed by GABA and 5-HT immunocytochemistry. In cultures maintained in the presence of BDNF (10 ng/ml), the density of TH-positive cells was increased by 2.5-fold (P F 0.05), and the TH-positive fiber density was increased by 3.5-fold (P F 0.01), relative to control cultures. Similarly, the relative increases in DA content and TH activity were 2.6- and 2.3-fold, respectively, in the BDNF-treated cultures (P F 0.01 and P F 0.01). On a per neuron basis, DA content and TH activity were not markedly changed by BDNF treatment, suggesting that the increases in DA content and TH activity are due to more DA neurons surviving. Relative elevations were also observed in serotonin content (2.0-fold, P F 0.01) and GAD enzymatic activity (1.4-fold, P F 0.01). Future studies will need to determine whether these changes result from the direct action of BDNF on these neurons or through some indirect mechanism. The results demonstrate that BDNF has beneficial effects on cultured human fetal tissue, which may be relevant in optimizing neuronal transplantation techniques, and that multiple systems are simultaneously influenced by BDNF.
在人胎儿腹侧中脑的游离滚动管培养物中,检测了神经营养因子脑源性神经营养因子(BDNF)促进多巴胺能、5-羟色胺能和γ-氨基丁酸能神经元存活及调节其表型标志物表达的能力。该培养系统包含黑质原基的神经元以及延髓缝际核的神经元。通过酪氨酸羟化酶(TH)免疫细胞化学监测多巴胺能神经元数量和TH纤维密度。将多巴胺(DA)含量、TH酶活性、5-羟色胺(5-HT)含量和谷氨酸脱羧酶(GAD)活性的测定用作各自神经递质功能的指标。通过GABA和5-HT免疫细胞化学证实了该培养系统中存在γ-氨基丁酸能和5-羟色胺能神经元。相对于对照培养物,在存在BDNF(10 ng/ml)的培养物中,TH阳性细胞密度增加了2.5倍(P<0.05),TH阳性纤维密度增加了3.5倍(P<0.01)。同样,在BDNF处理的培养物中,DA含量和TH活性的相对增加分别为2.6倍和2.3倍(P<0.01和P<0.01)。基于单个神经元,BDNF处理并未使DA含量和TH活性发生明显变化,这表明DA含量和TH活性的增加是由于更多的DA能神经元存活所致。5-羟色胺含量(2.0倍,P<0.01)和GAD酶活性(1.4倍,P<0.01)也观察到相对升高。未来的研究需要确定这些变化是由BDNF对这些神经元的直接作用还是通过某种间接机制引起的。结果表明,BDNF对培养的人胎儿组织具有有益作用,这可能与优化神经元移植技术相关,并且多个系统同时受到BDNF的影响。