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Vitrification of mouse embryo-derived ICM cells: a tool for preserving embryonic stem cell potential?

机译:小鼠胚胎来源的ICM细胞的玻璃化:保存胚胎干细胞潜能的工具?

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PURPOSE: Vitrification technology presents new opportunities for preservation of embryo derived stem cells without first establishing a viable ESC line. This study tests the feasibility of cryopreserving ICM cells using vitrification. MATERIALS AND METHODS: ICMs from mouse embryos were isolated and vitrified in HSV straws or on cryoloops. Upon warming, the vitrified ICMs were cultured and observed for attachment and morphology. Colonies were passaged every 3-6 days. ICMs and ICM-derived ESC colonies were tested for expression of stem cell specific markers. RESULTS: ICMs vitrified on both the cryoloop and the HSV straw had high survival rates. ICM derived ESCs remained undifferentiated for several passages and demonstrated expression of typical stem cell markers; SSEA-1, Sox-2, Oct 4 and alkaline phosphatase. CONCLUSION: This is the first report on successful vitrification of isolated ICMs and the subsequent derivation of ESC colonies. Vitrification of isolated ICMs is a novel approach for preservation of the "stem cell source" material.
机译:目的:玻璃化技术为保存胚胎衍生干细胞提供了新的机会,而无需首先建立可行的ESC系。这项研究测试了使用玻璃化冷冻保存ICM细胞的可行性。材料与方法:从小鼠胚胎中分离出ICM,并在HSV吸管或冷冻环中玻璃化。加热后,培养玻璃化的ICM,并观察其附着和形态。每3-6天传一次菌落。测试了ICM和源自ICM的ESC菌落的干细胞特异性标志物的表达。结果:冷冻环和HSV吸管上均玻璃化的ICM具有较高的存活率。 ICM衍生的胚胎干细胞保持几代未分化,并证明了典型干细胞标志物的表达。 SSEA-1,Sox-2,Oct 4和碱性磷酸酶。结论:这是关于分离的ICM成功玻璃化和随后的ESC菌落衍生的首次报道。隔离的ICM的玻璃化是保存“干细胞来源”材料的一种新颖方法。

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