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人骨来源细胞(HBDCS)在体外成骨过程中的特征

The Characteristics Of Human Bone-Derived Cells (HBDCS) during osteogenesis in vitro.

作者信息

Wrobel Edyta, Leszczynska Joanna, Brzoska Edyta

机构信息

Department of Biophysics and Human Physiology, Faculty of Health Sciences, Medical University of Warsaw, ul. Chalubinskiego 5, 02-004, Warsaw, Poland.

Department of Cytology, Institute of Zoology, Faculty of Biology, University of Warsaw, ul. Miecznikowa 1, 02-096, Warsaw, Poland.

出版信息

Cell Mol Biol Lett. 2016 Nov 16;21:26. doi: 10.1186/s11658-016-0027-8. eCollection 2016.

Abstract

BACKGROUND

The primary human bone-derived cell culture technique is used as a model to study human osteogenesis. Compared to cell line cultures, primary osteoprogenitor and osteoblast cultures provide more complex information about osteogenesis, bone remodeling and regeneration than cell line cultures.

METHODS

In this study, we isolated human bone-derived cells (HBDCs) and promoted their differentiation into osteoblasts. The following parameters were evaluated: cell number and viability, total protein expression, alkaline phosphatase activity, collagenous matrix production and osteogenic genes expression, i.e., gene coding for type I collagen and alkaline phosphatase.

RESULTS

It was proved the results show that HBDCs intensively proliferate during the first 7 days of culture followed by differentiation accompanied by an increase in alkaline phosphatase activity. Moreover, it was observed that during the differentiation of HBDCs, the expression of integrin β1 increased.

CONCLUSIONS

The process was also accompanied by changes in cell shape and rearrangement of the actin cytoskeleton and focal contacts containing FAK and the integrin β1 subunit. We suggest that the β1 integrin subunit may be a suitable new target in studies of the differentiation of primary human osteoblasts in culture.

摘要

背景

原代人骨来源细胞培养技术被用作研究人类骨生成的模型。与细胞系培养相比,原代骨祖细胞和成骨细胞培养比细胞系培养提供了更多关于骨生成、骨重塑和再生的复杂信息。

方法

在本研究中,我们分离了人骨来源细胞(HBDCs)并促进其向成骨细胞分化。评估了以下参数:细胞数量和活力、总蛋白表达、碱性磷酸酶活性、胶原基质产生和成骨基因表达,即编码I型胶原和碱性磷酸酶的基因。

结果

结果表明,HBDCs在培养的前7天强烈增殖,随后分化并伴随着碱性磷酸酶活性增加。此外,观察到在HBDCs分化过程中,整合素β1的表达增加。

结论

该过程还伴随着细胞形状的变化以及肌动蛋白细胞骨架和含有FAK和整合素β1亚基的粘着斑的重排。我们认为,β1整合素亚基可能是原代人成骨细胞培养分化研究中的一个合适的新靶点。

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