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单链DNA结合蛋白Ssbp3诱导小鼠胚胎干细胞分化为滋养层样细胞。

Single-stranded DNA binding protein Ssbp3 induces differentiation of mouse embryonic stem cells into trophoblast-like cells.

作者信息

Liu Jifeng, Luo Xinlong, Xu Yanli, Gu Junjie, Tang Fan, Jin Ying, Li Hui

机构信息

Laboratory of Molecular Developmental Biology, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.

Present address: KU Leuven Department of Development and Regeneration, Stem Cell Institute Leuven, Herestraat 49, 3000, Leuven, Belgium.

出版信息

Stem Cell Res Ther. 2016 May 28;7(1):79. doi: 10.1186/s13287-016-0340-1.

Abstract

BACKGROUND

Intrinsic factors and extrinsic signals which control unlimited self-renewal and developmental pluripotency in embryonic stem cells (ESCs) have been extensively investigated. However, a much smaller number of factors involved in extra-embryonic trophoblast differentiation from ESCs have been studied. In this study, we investigated the role of the single-stranded DNA binding protein, Ssbp3, for the induction of trophoblast-like differentiation from mouse ESCs.

METHODS

Gain- and loss-of-function experiments were carried out through overexpression or knockdown of Ssbp3 in mouse ESCs under self-renewal culture conditions. Expression levels of pluripotency and lineage markers were detected by real-time quantitative reverse-transcription polymerase chain reaction (qRT-PCR) analyses. The global gene expression profile in Ssbp3-overexpressing cells was determined by affymetrix microarray. Gene ontology and pathway terms were analyzed and further validated by qRT-PCR and Western blotting. The methylation status of the Elf5 promoter in Ssbp3-overexpressing cells was detected by bisulfite sequencing. The trophoblast-like phenotype induced by Ssbp3 was also evaluated by teratoma formation and early embryo injection assays.

RESULTS

Forced expression of Ssbp3 in mouse ESCs upregulated expression levels of lineage-associated genes, with trophoblast cell markers being the highest. In contrast, depletion of Ssbp3 attenuated the expression of trophoblast lineage marker genes induced by downregulation of Oct4 or treatment with BMP4 and bFGF in ESCs. Interestingly, global gene expression profiling analysis indicated that Ssbp3 overexpression did not significantly alter the transcript levels of pluripotency-associated transcription factors. Instead, Ssbp3 promoted the expression of early trophectoderm transcription factors such as Cdx2 and activated MAPK/Erk1/2 and TGF-β pathways. Furthermore, overexpression of Ssbp3 reduced the methylation level of the Elf5 promoter and promoted the generation of teratomas with internal hemorrhage, indicative of the presence of trophoblast cells.

CONCLUSIONS

This study identifies Ssbp3, a single-stranded DNA binding protein, as a regulator for mouse ESCs to differentiate into trophoblast-like cells. This finding is helpful to understand the regulatory networks for ESC differentiation into extra-embryonic lineages.

摘要

背景

控制胚胎干细胞(ESC)无限自我更新和发育多能性的内在因素和外在信号已得到广泛研究。然而,涉及ESC向胚外滋养层细胞分化的相关因素研究较少。在本研究中,我们探究了单链DNA结合蛋白Ssbp3在诱导小鼠ESC向滋养层样细胞分化中的作用。

方法

在自我更新培养条件下,通过过表达或敲低小鼠ESC中的Ssbp3进行功能获得和功能缺失实验。通过实时定量逆转录聚合酶链反应(qRT-PCR)分析检测多能性和谱系标志物的表达水平。通过Affymetrix微阵列确定Ssbp3过表达细胞中的全局基因表达谱。对基因本体和通路术语进行分析,并通过qRT-PCR和蛋白质免疫印迹进一步验证。通过亚硫酸氢盐测序检测Ssbp3过表达细胞中Elf5启动子的甲基化状态。还通过畸胎瘤形成和早期胚胎注射试验评估Ssbp3诱导的滋养层样表型。

结果

在小鼠ESC中强制表达Ssbp3会上调谱系相关基因的表达水平,其中滋养层细胞标志物的表达水平最高。相反,敲低Ssbp3会减弱ESC中因Oct4下调或用BMP4和bFGF处理而诱导的滋养层谱系标志物基因的表达。有趣的是,全局基因表达谱分析表明,Ssbp3过表达并未显著改变多能性相关转录因子的转录水平。相反,Ssbp3促进了早期滋养外胚层转录因子如Cdx2的表达,并激活了MAPK/Erk1/2和TGF-β信号通路。此外Ssbp3过表达降低了Elf5启动子的甲基化水平,并促进了出现内部出血的畸胎瘤的生成,这表明存在滋养层细胞。

结论

本研究确定单链DNA结合蛋白Ssbp3是小鼠ESC分化为滋养层样细胞的调节因子。这一发现有助于理解ESC分化为胚外谱系的调控网络。

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