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人端粒酶逆转录酶永生化人骨髓间充质干细胞向软骨细胞的分化

[Differentiation of human telomerase reverse transcriptase immortalized human marrow mesenchymal stem cell into chondrocyte].

作者信息

Qi Zhi-Ming, Lü Gang, Bai Yan-Dong, Wang Hong, Wang Ling

机构信息

Department of Orthopaedics, the First Affiliated Hospital of Medical University of China, Shenyang 110001, China.

出版信息

Zhonghua Wai Ke Za Zhi. 2008 May 1;46(9):697-9.

Abstract

OBJECTIVE

To establish an immortalized marrow mesenchymal stem cell line to facilitate advances in cartilage engineering research.

METHODS

Human telomerase reverse transcriptase (hTERT) cDNA was transferred into primary human marrow mesenchymal stem cells (hMSC) by retroviral vector pLEGFP-C1-hTERT. Subsequently G418 resistant cell clone was screened and expanded for further studies. hMSC biomarkers and hTERT expression were confirmed by examination. Transfected hMSC was induced to differentiate into chondrocyte using TGF-P1 and dexamethasone.

RESULTS

Up-regulated hTERT expression was detected in transfected hMSC. hMSC-hTERT cells could be induced to differentiate into chondrocyte. Higher telomerase activity in transfected cells was maintained for 50 population doublings so far. Collagen II could be detected in induced transfected hMSC by immunocytochemical and hybridization in situ.

CONCLUSIONS

Ectopic expression of hTERT can effectively immortalize hMSC in vitro. Immortalized hMSC can be induced to differentiate into chondrocyte under certain condition. It may be an ideal target of further studies in cartilage engineering.

摘要

目的

建立永生化骨髓间充质干细胞系,以促进软骨工程研究的进展。

方法

通过逆转录病毒载体pLEGFP-C1-hTERT将人端粒酶逆转录酶(hTERT)cDNA导入原代人骨髓间充质干细胞(hMSC)。随后筛选并扩增G418抗性细胞克隆以进行进一步研究。通过检测确认hMSC生物标志物和hTERT表达。使用TGF-β1和地塞米松诱导转染的hMSC分化为软骨细胞。

结果

在转染的hMSC中检测到hTERT表达上调。hMSC-hTERT细胞可被诱导分化为软骨细胞。到目前为止,转染细胞中较高的端粒酶活性维持了50次群体倍增。通过免疫细胞化学和原位杂交在诱导的转染hMSC中可检测到Ⅱ型胶原。

结论

hTERT的异位表达可有效使hMSC在体外永生化。永生化的hMSC在一定条件下可被诱导分化为软骨细胞。它可能是软骨工程进一步研究的理想靶点。

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