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白血病抑制因子对小鼠胚胎干细胞建立和维持的需求。

Requirement of leukemia inhibitory factor for establishing and maintaining embryonic stem cells in mice.

作者信息

Lee Jae Hee, Lee Eun Ju, Lee Chae Hyun, Park Jun Hong, Han Jae Yong, Lim Jeong Mook

机构信息

Department of Agricultural Biotechnology, Seoul National University, Seoul, Korea.

Clinical Research Institute, Seoul National University, Seoul, Korea.

出版信息

Fertil Steril. 2009 Sep;92(3):1133-1140. doi: 10.1016/j.fertnstert.2008.07.1733. Epub 2008 Sep 30.

Abstract

OBJECTIVE

To evaluate the necessity of leukemia inhibitory factor (LIF) in establishing and self-renewing embryonic stem cells (ESCs).

DESIGN

Prospective animal model study.

SETTING

Gamete and Stem Cell Biotechnology Laboratory, Seoul National University, Korea.

ANIMAL(S): F1 hybrid B6D2F1 mice.

INTERVENTION(S): Inner cell mass (ICM) cells of blastocysts were cultured or commercially available ESCs were maintained in LIF-free or LIF-containing medium on mouse embryonic fibroblast (MEF) feeder.

MAIN OUTCOME MEASURE(S): Cell morphology, LIF concentration, and mRNA expression.

RESULT(S): The MEFs themselves secreted 146.5-175.3 pg/mL LIF in LIF-free medium. The ICM cells formed ESC-like colonies on MEF feeder, and E14 and R1 ESCs were successfully maintained in LIF-free medium. Expression of the genes either mediating LIF function or regulating stemness was not altered significantly, and change in the growth of ESCs was not prominent in LIF-free medium. Neither mRNA expression of differentiation-related genes nor differentiation into embryoid body was changed in the ESCs.

CONCLUSION(S): Addition of LIF to culture medium is not necessary for establishing ICM-derived ESC-like colonies in the presence of fibroblast monolayer, and established ESCs can be maintained in an LIF-free medium.

摘要

目的

评估白血病抑制因子(LIF)在建立和自我更新胚胎干细胞(ESC)中的必要性。

设计

前瞻性动物模型研究。

地点

韩国首尔国立大学配子与干细胞生物技术实验室。

动物

F1杂种B6D2F1小鼠。

干预措施

将囊胚的内细胞团(ICM)细胞进行培养,或将市售的ESC在不含LIF或含LIF的培养基中,置于小鼠胚胎成纤维细胞(MEF)饲养层上进行培养。

主要观察指标

细胞形态、LIF浓度和mRNA表达。

结果

MEF自身在不含LIF的培养基中分泌146.5 - 175.3 pg/mL的LIF。ICM细胞在MEF饲养层上形成了ESC样集落,并且E14和R1 ESC在不含LIF的培养基中成功维持培养。介导LIF功能或调节干性的基因表达没有显著改变,在不含LIF的培养基中ESC的生长变化也不明显。ESC中分化相关基因的mRNA表达和向胚状体的分化均未改变。

结论

在存在成纤维细胞单层的情况下,向培养基中添加LIF对于建立源自ICM的ESC样集落并非必要,并且已建立的ESC可以在不含LIF的培养基中维持培养。

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