TiO2coating promotes human mesenchymal stem cell proliferation without the loss of their capacity for chondrogenic differentiation

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 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]
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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