Department of OB-GYN, Cleveland Clinic Foundation, Women's Health Institute, Beachwood, OH, USA.
J Assist Reprod Genet. 2011 Feb;28(2):93-9. doi: 10.1007/s10815-010-9500-x. Epub 2010 Nov 6.
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.
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.
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.
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.
玻璃化技术为胚胎衍生干细胞的保存提供了新的机会,而无需首先建立可行的 ESC 系。本研究测试了使用玻璃化法冷冻保存 ICM 细胞的可行性。
从小鼠胚胎中分离出 ICM 细胞,并在 HSV 吸管或 cryoloop 上进行玻璃化处理。解冻后,对冷冻的 ICM 进行培养,并观察其附着和形态。每隔 3-6 天传代一次。对 ICM 和 ICM 衍生的 ESC 集落进行干细胞特异性标志物的检测。
在 cryoloop 和 HSV 吸管上进行玻璃化处理的 ICM 存活率均较高。ICM 衍生的 ESC 在几轮传代后仍保持未分化状态,并表现出典型的干细胞标志物的表达;SSEA-1、Sox-2、Oct 4 和碱性磷酸酶。
这是首次成功报告对分离的 ICM 进行玻璃化处理,并随后衍生出 ESC 集落。分离的 ICM 玻璃化处理是保存“干细胞来源”材料的一种新方法。