[bfgf刺激的mef条件培养基能够维持人类胚胎干细胞]。

Yi Ping Zhou, Anne Rochat, Antoinette Hatzfeld, Isabelle Peiffer, Romain Barbet, Jacques Hatzfeld, Ma Lin Li
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引用次数: 0

摘要

4 ng/ml bFGF是小鼠胚胎成纤维细胞(MEF)培养hESC所必需的,退出bFGF可促进hESC分化。为了研究bFGF对MEF的影响,我们收集了一系列MEF条件培养基(bFGF- mcm),分别以0.03、0.1、0.3、1和4 ng/ml的bFGF浓度分别培养MEF。用形态学和碱性磷酸酶染色法测定bFGF-MCM培养hESC的原始性。与对照培养基(无bFGF: MCM培养基)相比,未分化菌落比例分别由23%提高到29%、44%、74%、77%和78%。而空白培养基(含bFGF但不含MEF的培养基:bFGF- sr)中未分化菌落的百分比为13% ~ 31%。说明低浓度bFGF作用于MEF,刺激MEF产生维持hESC的有效条件培养基。确定有效条件介质中的活性因子有助于了解hESC自我更新的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[bFGF-stimulated MEF-conditioned medium is capable of maintaining human embryonic stem cells].

4 ng/ml bFGF is indispensable for hESC cultured on mouse embryonic fibroblasts (MEF), withdrawal of bFGF drives the hESC to differentiate. In order to exploit effect of bFGF on MEF, we collected a series of MEF conditioned medium (bFGF-MCM) by co-culturing MEF with increasing bFGF concentrations: 0.03, 0.1, 0.3, 1 and 4 ng/ml. The primitivity of hESC cultured in bFGF-MCM was estimated by morphology and alkaline phosphatase staining. Compared with the control medium (medium conditioned without bFGF: MCM), percentage of undifferentiated colony was increased from 23% to 29%, 44%, 74%, 77% and 78%, respectively. However, percentage of undifferentiated colony in the blank medium (medium conditioned with bFGF but without MEF: bFGF-SR) was from 13% to 31%. This indicated that low concentration of bFGF acted on MEF and stimulated MEF producing effective conditioned medium for maintaining hESC. To identify active elements in the effective conditioned medium can help to understand mechanisms of hESC self-renewal.

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