Schlumpf M, Shoemaker W J, Bloom F E
Proc Natl Acad Sci U S A. 1977 Oct;74(10):4471-5. doi: 10.1073/pnas.74.10.4471.
Norepinephrine (NE)-producing cells of the nucleus locus ceruleus and dopamine (DA)-producing cells of the substantia nigra were dissected microscopically from embryonic rat brain, explanted, and maintained in culture for up to 5 weeks. The cultured neurons of both brain regions showed normal maturation of axons and dendrites and formed ultrastructurally defined synaptic contacts. Fluorescence microscopy of cultured neurons from both brain regions showed typical in situ cytological features: long axonal processes with multiple varicosities for locus ceruleus cultures, and smooth, wispy nonvaricose processes in the substantia nigra cultures. All cultures processed for fluorescence microscopy contained specific catecholamine-fluorescent cells. By radioenzyme assay for catecholamines, more than half of the locus ceruleus cultures contained measurable (>10 pg) quantities of NE and DA, but, unlike results on intact brains, DA content exceeded NE content. Cultures of substantia nigra neurons retained no NE and very little DA. Media from substantia nigra and locus ceruleus cultures contained substantial quantities of DA. Addition of reserpine (10 muM) to the medium depleted locus ceruleus neurons of both amines. The long survival time in culture of locus ceruleus cells, the normal appearance of fluorescent cell bodies and processes, the apparent development of morphologically specialized interneuronal connections, and the ability to synthesize and store NE make these cultures ideally suited for neurophysiological recording as well as morphological, biochemical, and pharmacological experiments.
从胚胎大鼠脑中通过显微镜解剖出蓝斑核中产生去甲肾上腺素(NE)的细胞和黑质中产生多巴胺(DA)的细胞,进行体外培养,培养长达5周。两个脑区的培养神经元均显示出轴突和树突的正常成熟,并形成了超微结构明确的突触连接。对两个脑区培养神经元的荧光显微镜检查显示出典型的原位细胞学特征:蓝斑核培养物中有带有多个膨体的长轴突,黑质培养物中有光滑、纤细无膨体的轴突。所有用于荧光显微镜检查的培养物中都含有特定的儿茶酚胺荧光细胞。通过儿茶酚胺的放射酶测定法,超过一半的蓝斑核培养物中含有可测量的(>10 pg)NE和DA,但与完整大脑的结果不同,DA含量超过NE含量。黑质神经元培养物中未保留NE且仅含有极少量的DA。黑质和蓝斑核培养物的培养基中含有大量的DA。向培养基中添加利血平(10 μM)可耗尽蓝斑核神经元中的两种胺类。蓝斑核细胞在培养中的长时间存活、荧光细胞体和轴突的正常外观、形态学上特化的神经元间连接的明显发育以及合成和储存NE的能力,使得这些培养物非常适合进行神经生理学记录以及形态学、生物化学和药理学实验。