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人脐带血间充质干细胞与软骨细胞共培养时促进软骨形成。

Human Umbilical Cord Blood-Derived Mesenchymal Stem Cells Contribute to Chondrogenesis in Coculture with Chondrocytes.

作者信息

Li Xingfu, Duan Li, Liang Yujie, Zhu Weimin, Xiong Jianyi, Wang Daping

机构信息

Shenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People's Hospital (The First Hospital Affiliated to Shenzhen University), Shenzhen, Guangdong 518035, China; Department of Orthopedics, Shenzhen Second People's Hospital (The First Hospital Affiliated to Shenzhen University), Shenzhen, Guangdong 518035, China.

Department of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong; School of Chemical Biology & Biotechnology, Peking University Shenzhen Graduate School, Shenzhen, Guangdong 518055, China.

出版信息

Biomed Res Int. 2016;2016:3827057. doi: 10.1155/2016/3827057. Epub 2016 Jun 30.

Abstract

Human umbilical cord blood-derived mesenchymal stem cells (hUCB-MSCs) have been shown as the most potential stem cell source for articular cartilage repair. In this study, we aimed to develop a method for long-term coculture of human articular chondrocytes (hACs) and hUCB-MSCs at low density in vitro to determine if the low density of hACs could enhance the hUCB-MSC chondrogenic differentiation as well as to determine the optimal ratio of the two cell types. Also, we compared the difference between direct coculture and indirect coculture at low density. Monolayer cultures of hUCB-MSCs and hACs were investigated at different ratios, at direct cell-cell contact groups for 21 days. Compared to direct coculture, hUCB-MSCs and hACs indirect contact culture significantly increased type II collagen (COL2) and decreased type I collagen (COL1) protein expression levels. SRY-box 9 (SOX9) mRNA levels and protein expression were highest in indirect coculture. Overall, these results indicate that low density direct coculture induces fibrocartilage. However, indirect coculture in conditioned chondrocyte cell culture medium can increase expression of chondrogenic markers and induce hUCB-MSCs differentiation into mature chondrocytes. This work demonstrates that it is possible to promote chondrogenesis of hUCB-MSCs in combination with hACs, further supporting the concept of novel coculture strategies for tissue engineering.

摘要

人脐带血间充质干细胞(hUCB - MSCs)已被证明是关节软骨修复最具潜力的干细胞来源。在本研究中,我们旨在开发一种在体外以低密度长期共培养人关节软骨细胞(hACs)和hUCB - MSCs的方法,以确定hACs的低密度是否能增强hUCB - MSC的软骨形成分化以及确定两种细胞类型的最佳比例。此外,我们比较了低密度下直接共培养和间接共培养之间的差异。在不同比例下对hUCB - MSCs和hACs进行单层培养,在直接细胞 - 细胞接触组中培养21天。与直接共培养相比,hUCB - MSCs和hACs间接接触培养显著增加了II型胶原蛋白(COL2)的表达并降低了I型胶原蛋白(COL1)的蛋白表达水平。SRY盒9(SOX9)的mRNA水平和蛋白表达在间接共培养中最高。总体而言,这些结果表明低密度直接共培养诱导纤维软骨形成。然而,在条件性软骨细胞培养基中间接共培养可增加软骨形成标志物的表达并诱导hUCB - MSCs分化为成熟软骨细胞。这项工作表明,将hUCB - MSCs与hACs联合可促进其软骨形成,进一步支持了组织工程新型共培养策略的概念。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/047d/4944057/899a7c7adf6c/BMRI2016-3827057.001.jpg

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