Sakagami Hiroshi, Suzuki Ryuichiro, Shirataki Yoshiaki, Iwama Soichi, Nakagawa Mika, Suzuki Hayato, Tanaka Kenta, Tamura Nobuaki, Takeshima Hiroshi
Meikai University Research Institute of Odontology (M-RIO), Saitama, Japan
Faculty of Pharmacy and Pharmaceutical Sciences, Josai University, Saitama, Japan
In Vivo. 2017 Nov-Dec;31(6):1089-1095. doi: 10.21873/invivo.11174.
BACKGROUND/AIM: Most of the previous investigators have used various types of media for the culture of nerve cells. In order to optimize the culture conditions, we compared the growth rate and amino acid consumption by two popular neuron models, rat PC12 and human SH-SY5Y, grown in DMEM or DMEM: Ham's F-12 (1:1): non-essential amino acids, supplemented with 10% fetal bovine serum (referred to DMEM and Mix, respectively).
Cell growth was monitored by the MTT method. Amino acids in the culture medium were quantitated by amino acid analysis after deproteinization.
Efficient cell attachment could be achieved even if PC12 cells were inoculated at extreme lower cell density in a non-coated plain dish, without addition of its condition medium. Both PC12 and SH-SY5Y cells proliferated up to slightly higher cell density in DMEM than in Mix. Approximately 2-fold higher utilization rate of glutamine and essential amino acids was observed in DMEM. Amyloid peptides such as Aβ and Aβ suppressed their growth nearly by 50%.
The present study suggests the usefulness of DMEM for the study of searching neuroprotective substances, based on its favorable effects on cell attachment, cell growth and amino acid utilization as well as amyloid peptide sensitivity.
背景/目的:此前大多数研究者使用各种类型的培养基来培养神经细胞。为了优化培养条件,我们比较了两种常用神经元模型(大鼠PC12和人SH-SY5Y)在添加10%胎牛血清的DMEM或DMEM:Ham's F-12(1:1):非必需氨基酸(分别称为DMEM和混合培养基)中生长时的生长速率和氨基酸消耗情况。
采用MTT法监测细胞生长。通过对培养基进行脱蛋白处理后进行氨基酸分析来定量培养基中的氨基酸。
即使在未包被的普通培养皿中以极低的细胞密度接种PC12细胞,且不添加其条件培养基,也能实现高效的细胞贴壁。PC12和SH-SY5Y细胞在DMEM中的增殖密度均略高于在混合培养基中的增殖密度。在DMEM中观察到谷氨酰胺和必需氨基酸的利用率大约高出2倍。淀粉样肽如Aβ和Aβ可使它们的生长抑制近50%。
本研究表明,基于DMEM对细胞贴壁、细胞生长、氨基酸利用以及淀粉样肽敏感性的有利影响,其在寻找神经保护物质的研究中具有实用性。