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利用活细胞中总ATP含量的测定对人神经干/祖细胞增殖的外源性因子进行体外筛选

In Vitro Screening of Exogenous Factors for Human Neural Stem/Progenitor Cell Proliferation Using Measurement of Total ATP Content in Viable Cells.

作者信息

Kanemura Yonehiro, Mori Hideki, Nakagawa Atsuyo, Islam Mohammed Omedul, Kodama Eri, Yamamoto Atsuyo, Shofuda Tomoko, Kobayashi Satoshi, Miyake Jun, Yamazaki Tomohiko, Hirano Shun-Ichiro, Yamasaki Mami, Okano Hideyuki

机构信息

Research Institute for Cell Engineering, National Institute of Advanced Industrial Science and Technology, 3-11-46 Nakoji, Amagasaki, Hyogo 661-0974, Japan.

Institute for Clinical Research, Osaka National Hospital, National Hospital Organization, Osaka 540-0006, Japan.

出版信息

Cell Transplant. 2005 Oct;14(9):673-682. doi: 10.3727/000000005783982701.

Abstract

One of the newest and most promising methods for treating intractable neuronal diseases and injures is the transplantation of ex vivo-expanded human neural stem/progenitor cells (NSPCs). Human NSPCs are selectively expanded as free-floating neurospheres in serum-free culture medium containing fibroblast growth factor 2 (FGF2) and/or epidermal growth factor (EGF); however, the culture conditions still need to be optimized for performance and cost before the method is used clinically. Here, to improve the NSPC culture method for clinical use, we used an ATP assay to screen the effects of various reagents on human NSPC proliferation. Human NSPCs responded to EGF, FGF2, and leukemia inhibitory factor (LIF) in a dose-dependent manner, and the minimum concentrations eliciting maximum effects were 10 ng/ml EGF, 10 ng/ml FGF2, and 5 ng/ml LIF. EGF and LIF were stable in culture medium without NSPCs, although FGF2 was degraded. In the presence of human NSPCs, however, FGF2 and LIF were both degraded very rapidly, to below the estimated minimum concentration on day 3, but EGF remained above the minimum concentration for 5 days. Adding supplemental doses of each growth factor during the incubation promoted human NSPC proliferation. Among other supplements, insulin and transferrin promoted human NSPC growth, but progesterone, putrescine, selenite, D-glucose, and lactate were not effective and were cytotoxic at higher concentrations. Supplementing with conditioned medium from human NSPCs significantly increased human NSPC proliferation, but using a high percentage of the medium had a negative effect. These findings suggest that human NSPC culture is regulated by a balance in the culture medium between decreasing growth factor levels and increasing positive or negative factors derived from the NSPCs. Thus, in designing culture conditions for human NSPCs, it is useful to take the individual properties of each factor into consideration.

摘要

治疗难治性神经疾病和损伤的最新且最具前景的方法之一是移植体外扩增的人神经干细胞/祖细胞(NSPCs)。人NSPCs在含有成纤维细胞生长因子2(FGF2)和/或表皮生长因子(EGF)的无血清培养基中作为悬浮神经球被选择性扩增;然而,在该方法临床应用之前,培养条件仍需在性能和成本方面进行优化。在此,为改进用于临床的NSPC培养方法,我们使用ATP测定法来筛选各种试剂对人NSPC增殖的影响。人NSPCs对EGF、FGF2和白血病抑制因子(LIF)呈剂量依赖性反应,引发最大效应的最低浓度分别为10 ng/ml EGF、10 ng/ml FGF2和5 ng/ml LIF。在没有NSPCs的培养基中,EGF和LIF是稳定的,尽管FGF2会降解。然而,在有人NSPCs存在的情况下,FGF2和LIF都迅速降解,到第3天降至估计的最低浓度以下,但EGF在5天内仍高于最低浓度。在培养期间添加各生长因子的补充剂量可促进人NSPC增殖。在其他补充剂中,胰岛素和转铁蛋白促进人NSPC生长,但孕酮、腐胺、亚硒酸盐、D -葡萄糖和乳酸无效,且在较高浓度下具有细胞毒性。用人NSPCs的条件培养基进行补充可显著增加人NSPC增殖,但使用高比例的该培养基有负面影响。这些发现表明,人NSPC培养受到培养基中生长因子水平降低与NSPCs衍生的正负因子增加之间平衡的调节。因此,在设计人NSPCs的培养条件时,考虑每个因子的个体特性是有用的。

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