软骨发生
间充质干细胞
CD44细胞
CD90型
细胞生长
阿格里坎
细胞生物学
生物医学工程
细胞分化
材料科学
细胞培养
干细胞
碱性磷酸酶
川地34
细胞
化学
分子生物学
病理
生物
医学
生物化学
骨关节炎
酶
基因
替代医学
遗传学
关节软骨
作者
Salla Kaitainen,Anssi J. Mähönen,Reijo Lappalainen,Heikki Kröger,Mikko J. Lammi,Chengjuan Qu
出处
期刊:Biofabrication
[IOP Publishing]
日期:2013-04-17
卷期号:5 (2): 025009-025009
被引量:29
标识
DOI:10.1088/1758-5082/5/2/025009
摘要
Human mesenchymal stem cells (hMSCs) are used in applications, which may require a large amount of cells; therefore, efficient expansion of the cells is desired. We studied whether TiO2 coating on plastic cell culture dishes could promote proliferation of hMSCs without adverse effects in chondrogenic differentiation. TiO2-films were deposited on polystyrene dishes and glass coverslips using an ultrashort pulsed laser deposition technique. Human MSCs from three donors were expanded on them until 95% confluence, and the cells were evaluated by morphology, immunocytochemistry and quantitative RT-PCR (qRT-PCR). The chondrogenic differentiation in pellets was performed after cultivation on TiO2-coated dishes. Chondrogenesis was evaluated by histological staining of proteoglycans and type II collagen, and qRT-PCR. Human MSC-associated markers STRO-1, CD44, CD90 and CD146 did not change after expansion on TiO2-coated coverslips. However, the cell number after a 48h-culture period was significantly higher on TiO2-coated culture dishes. Importantly, TiO2 coating caused no significant differences in the proteoglycan and type II collagen staining of the pellets, or the expression of chondrocyte-specific genes in the chondrogenesis assay. Thus, the proliferation of hMSCs could be significantly increased when cultured on TiO2-coated dishes without weakening their chondrogenic differentiation capacity. The transparency of TiO2-films allows easy monitoring of the cell growth and morphology under a phase-contrast microscope.
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