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人类胚胎干细胞的衍生、表征及分化:含血清与无血清培养基的比较及生殖细胞分化证据

Derivation, characterization and differentiation of human embryonic stem cells: comparing serum-containing versus serum-free media and evidence of germ cell differentiation.

作者信息

Chen H-F, Kuo H-C, Chien C-L, Shun C-T, Yao Y-L, Ip P-L, Chuang C-Y, Wang C-C, Yang Y-S, Ho H-N

机构信息

Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology and Infertility, College of Medicine and Hospital, National Taiwan University, Taipei, Taiwan.

出版信息

Hum Reprod. 2007 Feb;22(2):567-77. doi: 10.1093/humrep/del412. Epub 2006 Oct 27.

Abstract

BACKGROUND

This study was designed to establish human embryonic stem cell (hESC) lines, to identify the differences when maintained in serum-containing versus serum-free medium and to test their potential of in vitro differentiation.

METHODS

Procedures including immunosurgery were performed on 11 donated human blastocysts to establish hESC lines. The cell lines were characterized and maintained using either serum-free or serum-containing media to compare their morphology, Oct-4 expression, apoptosis and growth speed. Differentiation of these lines was evaluated by the morphology and the expression of genes belonging to the three embryonic germ layers and the germ cell lineage.

RESULTS

Three hESC lines were established, and they grew at similar speed in both media (serum-containing or serum-free), but hESC cultured in serum-containing medium yielded significantly higher percentages of morphologically good colonies and cells expressing Oct-4. These cell lines differentiated spontaneously in vitro into cells expressing markers belonging to all three embryonic germ layers and germ cell markers, including c-Kit, STELLA, VASA and growth differentiation factor 9 (GDF9), in directly adherent culture.

CONCLUSIONS

Three hESC lines with Taiwanese ancestry have been established, and they retain the in vitro differentiation potential with or without embryoid body (EB) formation. The data support that hESC may be capable of differentiation into germ cells although further confirmation is needed. It is also suggested that strategies such as stepwise adaptation will be needed before implementing a serum-free culture condition for hESC lines that have previously been derived in a medium containing serum.

摘要

背景

本研究旨在建立人胚胎干细胞(hESC)系,确定其在含血清培养基和无血清培养基中培养时的差异,并测试其体外分化潜能。

方法

对11个捐赠的人囊胚进行包括免疫外科手术在内的操作以建立hESC系。使用无血清或含血清培养基对细胞系进行鉴定和培养,以比较它们的形态、Oct-4表达、凋亡和生长速度。通过形态以及属于三个胚胎胚层和生殖细胞谱系的基因表达来评估这些细胞系的分化情况。

结果

建立了三个hESC系,它们在两种培养基(含血清或无血清)中的生长速度相似,但在含血清培养基中培养的hESC产生的形态良好的集落和表达Oct-4的细胞百分比显著更高。在直接贴壁培养中,这些细胞系在体外自发分化为表达属于所有三个胚胎胚层的标志物以及生殖细胞标志物的细胞,包括c-Kit、STELLA、VASA和生长分化因子9(GDF9)。

结论

已建立了三个具有台湾人血统的hESC系,无论有无形成胚状体(EB),它们都保留体外分化潜能。数据支持hESC可能能够分化为生殖细胞,尽管还需要进一步证实。还表明,对于先前在含血清培养基中获得的hESC系,在实施无血清培养条件之前,需要逐步适应培养等策略。

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