Abstract

The chemical composition and texture of titanium coatings can influence the growth characteristics of the adhered cells. An enhanced proliferation of the human mesenchymal stem cells (hMSCs) would be beneficial. The present study was aimed to investigate whether titanium deposited at different atmospheres would affect the cell growth properties, cellular morphology, and expression of surface markers of hMSCs. Titanium-based coatings were deposited on silicon wafers under oxygen, nitrogen, or argon atmospheres by ultra-short pulsed laser deposition using two different gas pressures followed by heating at 400 °C for 2 h. The characteristics of the coated surfaces were determined via contact angle, zeta potential, and scanning electron microscopy (SEM) techniques. Human MSCs were cultivated on differently coated silicon wafers for 48 h. Subsequently, the cell proliferation rates were analyzed with an MTT assay. The phenotype of hMSCs was checked via immunocytochemical stainings of MSC-associated markers CD73, CD90, and CD105, and the adhesion, spreading, and morphology of hMSCs on coated materials via SEM. The cell proliferation rates of the hMSCs were similar on all coated silicon wafers. The hMSCs retained the MSC phenotype by expressing MSC-associated markers and fibroblast-like morphology with cellular projections. Furthermore, no significant differences could be found in the size of the cells when cultured on all various coated surfaces. In conclusion, despite certain differences in the contact angles and the zeta potentials of various titanium-based coatings, no single coating markedly improved the growth characteristics of hMSCs.

Highlights

  • The concept of tissue engineering has made great advances in the field of regenerative medicine, with the idea of using biomaterials and cells to construct new tissues to replace damaged ones in the body

  • The human mesenchymal stem cells (hMSCs) have gained wide interest in cell-based tissue engineering of bone and articular cartilage, due to their multipotentiality to differentiate into osteoblasts and chondrocytes [28,35]

  • Our previous study showed that the proliferation rate of the hMSCs significantly increased when they were cultured on TiO2-coated cell culture dishes without loss of their capacity for chondrogenic differentiation [28]

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Summary

Introduction

The concept of tissue engineering has made great advances in the field of regenerative medicine, with the idea of using biomaterials and cells to construct new tissues to replace damaged ones in the body. The properties of human mesenchymal stem cells (hMSCs) provide potential for use in regenerative medicine as delivery vehicles for cell-based therapies [1]. They have been considered an alternative cell source for differentiated autologous chondrocytes due to their self-renewal and Materials 2016, 9, 827; doi:10.3390/ma9100827 www.mdpi.com/journal/materials. The number of hMSCs needed in clinical experiments can be up to 24 million [9]. It can take a rather long time until enough cells in the monolayer expansion culture for the needs of clinical operations are obtained

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