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将脐带间充质干细胞诱导分化为肝细胞

ifferentiation of umbilical cord mesenchymal stem cells into hepatocytes

中文摘要英文摘要

目的:将脐带间充质干细胞(UC-MSCs)诱导分化为肝细胞,研究其肝分化潜能,为其在肝组织工程中的应用提供依据。方法:将分离得到的UC-MSCs诱导分化为成脂细胞和成骨细胞,鉴定其多向分化潜能。利用HGF和FGF-4联合诱导的方法将其诱导分化为肝细胞,采用PAS染色检测肝分化后的细胞是否具有糖原储存能力;采用实时荧光定量RT-PCR检测肝细胞特异性基因ALB、AFP和CK-18的表达。结果:分离得到的UC-MSCs可以被诱导分化为成脂细胞和成骨细胞。PAS染色结果表明肝分化的细胞具有糖原储存能力。实时荧光定量RT-PCR结果表明肝分化的细胞表达肝细胞特异性基因ALB、AFP和CK-18。结论:分离得到的UC-MSCs能够被诱导分化为成脂细胞和成骨细胞,证明其具有多向分化潜能。在HGF和FGF-4的联合诱导下可被诱导分化为肝细胞,表达肝细胞特异性基因,并具有糖原储存能力,表明UC-MSCs可能被用于肝组织工程研究。

Objective: Mesenchymal stem cells derived from umbilical cord (UC-MSCs) were induced to differentiate into hepatocytes to study their hepatic differentiation potential and provide the basis for their use in liver tissue engineering. Methods: UC-MSCs were induced to differentiate into adipocytes and osteoblasts to confirm their multipotent differentiation potential. UC-MSCs were induced to differentiate into hepatocytes with HGF and FGF-4. Periodic acid-Schiff (PAS) staining was performed to detect glycogen storage capacity of the differentiated cells. The differentiated cells were examined for the expression of hepatocyte-specific genes ALB, AFP and CK-18 by real-time RT-PCR. Results: UC-MSCs were induced to differentiate into adipocytes and osteoblasts. PAS staining showed that hepatocytes differentiated from UC-MSCs had the ability of the glycogen storage. Real-time RT-PCR analysis showed that hepatocytes differentiated from UC-MSCs expressed the hapatocyte-specific genes ALB, AFP and CK-18. Conclusion: UC-MSCs can be induced to differentiate into adipocytes and osteoblasts, demonstrating that they have multipotent differentiation potential. HGF and FGF-4 can induce UC-MSCs to differentiate into hepatocytes, which may be used in liver tissue engineering.

魏星、李鹏山

基础医学生物工程学

脐带间充质干细胞成脂分化成骨分化肝分化

umbilical cord mesenchymal stem cellsadipogenic differentiationosteogenic differentiationhepatocyte differentiation

魏星,李鹏山.将脐带间充质干细胞诱导分化为肝细胞[EB/OL].(2013-12-06)[2025-08-02].http://www.paper.edu.cn/releasepaper/content/201312-163.点此复制

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