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将绿色荧光蛋白(GFP)报告基因靶向人类胚胎干细胞的MIXL1基因座可鉴定出人类原始条纹样细胞,并能够分离出原始造血前体细胞。

Targeting a GFP reporter gene to the MIXL1 locus of human embryonic stem cells identifies human primitive streak-like cells and enables isolation of primitive hematopoietic precursors.

作者信息

Davis Richard P, Ng Elizabeth S, Costa Magdaline, Mossman Anna K, Sourris Koula, Elefanty Andrew G, Stanley Edouard G

机构信息

Monash Immunology and Stem Cell Laboratories, Monash University, Clayton, Victoria, Australia.

出版信息

Blood. 2008 Feb 15;111(4):1876-84. doi: 10.1182/blood-2007-06-093609. Epub 2007 Nov 21.

Abstract

Differentiating human embryonic stem cells (HESCs) represent an experimental platform for establishing the relationships between the earliest lineages that emerge during human development. Here we report the targeted insertion in HESCs of sequences encoding green fluorescent protein (GFP) into the locus of MIXL1, a gene transiently expressed in the primitive streak during embryogenesis.(1,2) GFP fluorescence in MIXL1(GFP/)(w) HESCs differentiated in the presence of BMP4 reported the expression of MIXL1, permitting the identification of viable human primitive streak-like cells. The use of GFP as a reporter for MIXL1 combined with cell surface staining for platelet-derived growth factor receptor alpha (PDGFRalpha) enabled the isolation of a cell population that was highly enriched in primitive hematopoietic precursors, the earliest derivatives of the primitive streak. These experiments demonstrate the utility of MIXL1(GFP/w) HESCs for analyzing the previously inaccessible events surrounding the development of human primitive streak-like cells and their subsequent commitment to hematopoiesis.

摘要

分化中的人类胚胎干细胞(HESCs)代表了一个实验平台,用于建立人类发育过程中最早出现的谱系之间的关系。在此,我们报告了将编码绿色荧光蛋白(GFP)的序列靶向插入HESCs中MIXL1基因座的情况,MIXL1是一种在胚胎发生过程中于原条中短暂表达的基因。在BMP4存在的情况下分化的MIXL1(GFP/)(w) HESCs中的GFP荧光报告了MIXL1的表达,从而能够鉴定出有活力的人类原条样细胞。使用GFP作为MIXL1的报告基因并结合血小板衍生生长因子受体α(PDGFRα)的细胞表面染色,能够分离出一个高度富集原始造血前体细胞的细胞群体,这些细胞是原条的最早衍生物。这些实验证明了MIXL1(GFP/w) HESCs在分析围绕人类原条样细胞发育及其随后向造血分化的先前难以触及的事件方面的实用性。

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