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热休克诱导hTERT永生化间充质干细胞成骨分化增强

Heat shock-induced enhancement of osteoblastic differentiation of hTERT-immortalized mesenchymal stem cells.

作者信息

Nørgaard Rune, Kassem Moustapha, Rattan Suresh I S

机构信息

Laboratory of Cellular Ageing, Danish Centre for Molecular Gerontology, Department of Molecular Biology, University of Aarhus, Denmark.

出版信息

Ann N Y Acad Sci. 2006 May;1067:443-7. doi: 10.1196/annals.1354.063.

Abstract

Heat shock (HS)-induced stress response in human cells results in a variety of biological effects and is known to induce the transcription of heat-shock proteins, which help the cells to cope with different kinds of stress. We have studied the effects of HS on the differentiation of human mesenchymal stem cells (hMSCs) into osteoblastic cells. As a model for hMSCs we used a telomerase-immortalized hMSC line designated hMSC-TERT. Cells were exposed to 1 h HS at 41 degrees C, 42.5 degrees C, or 44 degrees C prior to incubation in a medium containing either 10(-8) M 1alpha,25-dihydroxy-vitamin-D(3) (calcitriol) or 10(-8) M calcitriol, 50 microg/mL L-ascorbic acid, and 10 mM beta-glycerophosphate followed by an analysis of induction of osteoblast differentiation and the formation of mineralized matrix, respectively. Our results indicate that the exposure of cells to mild heat stress enhances the extent of differentiation of hMSCs by 12% to 42%. These effects are an expression of the phenomenon of mild stress-induced hormesis.

摘要

热休克(HS)诱导的人类细胞应激反应会产生多种生物学效应,并且已知会诱导热休克蛋白的转录,热休克蛋白有助于细胞应对各种应激。我们研究了热休克对人间充质干细胞(hMSCs)向成骨细胞分化的影响。作为hMSCs的模型,我们使用了一种端粒酶永生化的hMSC系,命名为hMSC-TERT。在含有10(-8) M 1α,25-二羟基维生素D(3)(骨化三醇)或10(-8) M骨化三醇、50 μg/mL L-抗坏血酸和10 mM β-甘油磷酸的培养基中孵育之前,将细胞在41℃、42.5℃或44℃下暴露于1小时热休克,随后分别分析成骨细胞分化的诱导情况和矿化基质的形成。我们的结果表明,将细胞暴露于轻度热应激可使hMSCs的分化程度提高12%至42%。这些效应是轻度应激诱导的兴奋效应现象的一种表现。

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