首页> 美国卫生研究院文献>Frontiers in Cell and Developmental Biology >Adherent vs. Free-Floating Neural Induction by Dual SMAD Inhibition for Neurosphere Cultures Derived from Human Induced Pluripotent Stem Cells
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Adherent vs. Free-Floating Neural Induction by Dual SMAD Inhibition for Neurosphere Cultures Derived from Human Induced Pluripotent Stem Cells

机译:对人诱导的多能干细胞衍生的神经球培养物双重SMAD抑制的粘附与自由漂浮神经诱导。

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摘要

Keeping neural stem cells under proliferation, followed by terminal differentiation, can substantially increase the number of neurons generated. With regard to the usability of proliferating neurospheres (NSPHs) cultures, adherent induction protocols have not yet been studied in comparison to embryoid body (EB)-based protocols. To compare these proctocols, neural induction of human induced pluripotent stem cells was performed by dual SMAD inhibition under both adherent and free-floating EB culture conditions. After 10 days, we transferred cells to low-attachment culture plates and proliferated them as free-floating neurospheres. RNA was collected, transcribed to cDNA and analyzed for sonic hedgehog expression that plays an important role during proliferation process. NSPHs were analyzed by immunofluorescence imaging directly and upon continued differentiation. The EB-based approach yielded in higher numbers of cells expressing the neural stem cell marker Nestin, and showed in contrast to the adherent induction protocol increased expression levels of sonic hedgehog. Although improvements to culture consistency and reliability are desirable, the EB-based protocol appears to be superior to the adherent protocol for both, the proliferation and differentiation capacity.
机译:使神经干细胞处于增殖状态,然后进行终末分化,可以大大增加生成的神经元数量。关于增殖神经球(NSPH)培养的可用性,与基于胚状体(EB)的协议相比,尚未研究粘附诱导协议。为了比较这些方法,在贴壁和自由漂浮的EB培养条件下,通过双重SMAD抑制对人诱导的多能干细胞进行神经诱导。 10天后,我们将细胞转移至低附着力培养板,并以自由漂浮的神经球形式增殖。收集RNA,转录为cDNA,并分析在增殖过程中起重要作用的声波刺猬的表达。通过直接和连续分化的免疫荧光成像分析了NSPH。基于EB的方法产生了更多数量的表达神经干细胞标记物Nestin的细胞,并且表明与粘附诱导方案相反,声音刺猬的表达水平增加了。尽管需要提高培养的一致性和可靠性,但基于EB的方案在增殖和分化能力方面似乎都优于依附方案。

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