自然永生化小鼠胚胎成纤维细胞系支持人类胚胎干细胞生长。

Mavi Camarasa, Daniel Brison, Susan J Kimber, Alan H Handyside
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引用次数: 10

摘要

人胚胎干细胞(hESC)的生长依赖于饲养细胞释放的多种因子。其中一些已经被阐明,尽管还需要更多的研究来了解干细胞在培养中的维持生物学。传统上,原代小鼠胚胎成纤维细胞(pmef)被用作喂养层,小鼠和人类成纤维细胞系已被证明支持hESC的多能性和自我更新。在这里,我们报道了三种新的小鼠胚胎成纤维细胞系的衍生,meflum、meflut和meflut - tb,它们在生长和支持未分化hESCs方面具有不同的特性。MEFLU-TB能够支持新衍生的Man-1以及H1、hes -1、hes -7、hes -8和hes -9人胚胎干细胞系的持续生长。在50多次传代和加倍后,meflub - tb喂食者与早期传代小鼠胚胎成纤维细胞在支持未分化hESC生长方面的能力进行了比较。我们的研究结果反驳了先前的观点,即pmef随着传代的增加而失去支持hESC增殖的能力,并表明mefl - tb小鼠胚胎成纤维细胞系及其条件培养基具有支持hESC细胞系维持的潜力。此外,我们的研究结果清楚地表明,原代成纤维细胞的自发永生化可以在不添加任何化学物质或基因修饰的情况下在培养中实现。
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Naturally immortalised mouse embryonic fibroblast lines support human embryonic stem cell growth.

Human embryonic stem cell (hESC) growth is dependent on various factors released by feeder cells. Some of them have already been elucidated, although much research is still needed to understand the biology of stem cell maintenance in culture. Traditionally, primary mouse embryonic fibroblasts (PMEFs) have been used as feeder layers, and both murine and human fibroblast cell lines have been shown to support pluripotency and self-renewal of hESC. Here we report the derivation of three new mouse embryonic fibroblast cell lines, MEFLU-M, MEFLU-T, and MEFLU-TB, with different properties regarding growth and support for undifferentiated hESCs. MEFLU-TB is able to support continuous growth of the newly derived Man-1, as well as H1, HUES-1, HUES-7, HUES-8, and HUES-9 human embryonic stem cell lines. After more than 50 passages and doublings, MEFLU-TB feeders compare to early passage primary mouse embryonic fibroblasts in their ability to support undifferentiated hESC growth. Our results contradict a previous paradigm that PMEFs tend to lose their capacity to support proliferation of hESCs with increasing passages, and show that the MEFLU-TB mouse embryonic fibroblast cell line and its conditioned medium have the potential to support the maintenance of hESC lines. Also, our results clearly show that spontaneous immortalization of primary fibroblasts can be achieved in culture without any chemical addition or genetic modification.

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