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体外从R1小鼠胚胎干细胞中优化成骨分化方案。

Optimized osteogenic differentiation protocol from R1 mouse embryonic stem cells in vitro.

作者信息

Yu Yanhong, Al-Mansoori Layla, Opas Michal

机构信息

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, M5S 1A8 Canada.

Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, M5S 1A8 Canada; Department of Chemistry & Earth Sciences, College of Arts and Science, University of Qatar, P.O. Box 2713, Doha, Qatar.

出版信息

Differentiation. 2015 Jan-Feb;89(1-2):1-10. doi: 10.1016/j.diff.2014.12.003. Epub 2015 Jan 19.

Abstract

Embryonic stem cells (ESCs) are a unique model that allows the study of molecular pathways underlying commitment and differentiation. One such lineage is osteoblasts, which are responsible for forming bone tissue in the body. There are many osteogenic differentiation protocols in the literature utilizing different soluble factors. The goal of the present study was to increase the efficacy of our osteogenic differentiation protocol from R1 cells. We have studied the effects of the addition of the following factors: dexamethasone, retinoic acid, and peroxisome-proliferator-activated receptor-gamma inhibitor, which have been reported to enhance osteogenesis. We found that among the 6 different protocols that were tested, the addition of retinoic acid with later addition of dexamethasone gives the most enrichment of osteogenic lineage cells. Thus, our findings provide valuable guidelines for culture condition to differentiate mouse R1 ESCs to osteoblastic cells in vitro.

摘要

胚胎干细胞(ESCs)是一种独特的模型,可用于研究细胞定向分化和分化过程中潜在的分子途径。成骨细胞就是这样一种细胞谱系,它负责在体内形成骨组织。文献中有许多利用不同可溶性因子的成骨分化方案。本研究的目的是提高我们从R1细胞进行成骨分化方案的效率。我们研究了添加以下因子的效果:地塞米松、视黄酸和过氧化物酶体增殖物激活受体γ抑制剂,据报道这些因子可增强成骨作用。我们发现,在测试的6种不同方案中,先添加视黄酸后添加地塞米松能使成骨谱系细胞得到最大程度的富集。因此,我们的研究结果为体外将小鼠R1胚胎干细胞分化为成骨细胞的培养条件提供了有价值的指导方针。

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