Nagata K, Takei N, Nakajima K, Saito H, Kohsaka S
Department of Neurochemistry, National Institute of Neuroscience, Tokyo, Japan.
J Neurosci Res. 1993 Feb 15;34(3):357-63. doi: 10.1002/jnr.490340313.
We previously reported that microglial conditioned medium (Mic-CM) has a neurotrophic effect on cultured rat neocortical neurons [Nakajima et al. (1989): Biomed Res 10:411-423]. In order to investigate the interaction between microglia and neurons in more detail, we determined the effects of Mic-CM on the primary cultured mesencephalic neurons from 16-day embryonic rats. The addition of Mic-CM to the culture medium significantly enhanced the survivability of neurons and promoted neurite extension in a low cell-density culture condition. In a high cell-density culture condition, Mic-CM markedly increased dopamine uptake, which was quantified by assessing the specific [3H]dopamine uptake, and also increased the dopamine content of cultured cells. Furthermore, the number of mesencephalic dopaminergic neurons, which was determined by quantitative analysis of tyrosine hydroxylase (TH)-immunoreactive cells, increased significantly in the presence of Mic-CM. These results suggest that Mic-CM enhances survival or maturation of TH-positive neurons present in cultures of the embryonic mesencephalon and that these neurotrophic effects may be due to a diffusible factor(s) from microglia.
我们之前报道过,小胶质细胞条件培养基(Mic-CM)对培养的大鼠新皮层神经元具有神经营养作用[中岛等人(1989年):《生物医学研究》10:411 - 423]。为了更详细地研究小胶质细胞与神经元之间的相互作用,我们测定了Mic-CM对来自16日龄胚胎大鼠的原代培养中脑神经元的影响。在低细胞密度培养条件下,向培养基中添加Mic-CM可显著提高神经元的存活率并促进神经突生长。在高细胞密度培养条件下,Mic-CM显著增加了多巴胺摄取(通过评估特异性[3H]多巴胺摄取进行定量),还增加了培养细胞的多巴胺含量。此外,通过对酪氨酸羟化酶(TH)免疫反应性细胞进行定量分析确定的中脑多巴胺能神经元数量,在存在Mic-CM的情况下显著增加。这些结果表明,Mic-CM可增强胚胎中脑培养物中TH阳性神经元的存活或成熟,并且这些神经营养作用可能归因于小胶质细胞分泌的一种或多种可扩散因子。