Takeshima T, Johnston J M, Commissiong J W
Neural Transplantation Unit, LMCN-NINDS-NIH, Bethesda, Maryland 20892.
J Neurosci. 1994 Aug;14(8):4769-79. doi: 10.1523/JNEUROSCI.14-08-04769.1994.
We have established a primary neuronal culture of the embryonic day 14 rat, ventral mesencephalic region, centered on the A8, A9, and A10 dopaminergic nuclei (approximately 1.0 mm3 of tissue). At 16 hr after plating on a substrate of poly-D-lysine, in a serum-free or serum-supplemented growth medium, using a microisland culturing method, 95% of the cells stained positive for neuron-specific enolase, 20% for tyrosine hydroxylase, and < 5% for vimentin. When the growth medium was supplemented with 10% fetal calf serum, the percentage of tyrosine hydroxylase-positive neurons increased significantly (p < 0.05) at the 7th and 10th days in culture, compared with the percentage present at 16 hr after plating. When cultured in a serum-free growth medium, the percentage of tyrosine hydroxylase-positive neurons decreased to < 5% and to 0% by the 5th and 7th days, respectively, while the percentage of GABA-IR neurons increased. The addition of serum to the serum-free culture rescued dopaminergic neurons from death induced by serum deprivation. The effect of serum was dependent both on the time of addition after plating, and on the percentage added. When the cells were plated in a serum-free medium, on a confluent, type 1 astrocyte monolayer, prepared from the ventral mesencephalon of the embryonic day 16 rat, the survival of dopaminergic neurons increased significantly (p < 0.01) at DIV5, versus survival after plating on poly-D-lysine. Conditioned medium prepared from the same mesencephalic type 1 astrocyte monolayer also rescued dopaminergic neurons from death. The rescue mediated by the astrocyte monolayer or the conditioned medium was not inhibited by the mitotic inhibitor cytosine arabino furanoside (1.0 microM). Type 1 astrocyte monolayers and conditioned media prepared from the striatum and cerebral cortex of the embryonic day 16 rat had weaker trophic effects than those mediated by mesencephalic glia. We conclude that serum deprivation causes the selective death of dopaminergic neurons in a primary culture of the rat E14 ventral mesencephalon. Type 1 astrocytes or the conditioned medium from type 1 astrocytes can rescue dopaminergic neurons from death induced by serum deprivation.(ABSTRACT TRUNCATED AT 400 WORDS)
我们建立了胚胎第14天大鼠腹侧中脑区域的原代神经元培养物,该区域以A8、A9和A10多巴胺能核为中心(约1.0立方毫米组织)。在接种于聚-D-赖氨酸底物上16小时后,使用微岛培养法,在无血清或添加血清的生长培养基中培养,95%的细胞神经元特异性烯醇化酶染色呈阳性,20%的细胞酪氨酸羟化酶染色呈阳性,波形蛋白染色阳性的细胞<5%。当生长培养基中添加10%胎牛血清时,与接种后16小时时相比,培养第7天和第10天时酪氨酸羟化酶阳性神经元的百分比显著增加(p<0.05)。在无血清生长培养基中培养时,酪氨酸羟化酶阳性神经元的百分比在培养第5天和第7天时分别降至<5%和0%,而γ-氨基丁酸免疫反应阳性神经元的百分比增加。向无血清培养物中添加血清可挽救多巴胺能神经元因血清剥夺所致的死亡。血清的作用既取决于接种后添加的时间,也取决于添加的百分比。当细胞接种于由胚胎第16天大鼠腹侧中脑制备的汇合的1型星形胶质细胞单层上的无血清培养基中时,与接种于聚-D-赖氨酸上相比,培养第5天时多巴胺能神经元的存活率显著增加(p<0.01)。由相同的中脑1型星形胶质细胞单层制备的条件培养基也可挽救多巴胺能神经元免于死亡。由星形胶质细胞单层或条件培养基介导的挽救作用不受有丝分裂抑制剂阿糖胞苷(1.0微摩尔)的抑制。由胚胎第16天大鼠纹状体和大脑皮质制备的1型星形胶质细胞单层和条件培养基的营养作用比中脑胶质细胞介导的作用弱。我们得出结论,血清剥夺导致大鼠E14腹侧中脑原代培养物中多巴胺能神经元的选择性死亡。1型星形胶质细胞或1型星形胶质细胞的条件培养基可挽救多巴胺能神经元因血清剥夺所致的死亡。(摘要截短至400字)