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纳米级表面几何形状和固定在 TiO2 纳米管上的生长因子对间充质干细胞分化的协同控制。

Synergistic control of mesenchymal stem cell differentiation by nanoscale surface geometry and immobilized growth factors on TiO2 nanotubes.

机构信息

Department of Experimental Medicine I, Nikolaus-Fiebiger-Center of Molecular Medicine, Friedrich-Alexander-University of Erlangen-Nuremberg, Glueckstrasse 5, 91054 Erlangen, Germany.

出版信息

Small. 2012 Jan 9;8(1):98-107. doi: 10.1002/smll.201100790. Epub 2011 Nov 18.

Abstract

The aim of this study is to elucidate whether combined environmental signals provided by nanoscale topography and by growth factors control cell behavior of mesenchymal stem cells (MSCs) in a synergistic or simply additive manner. Chondrogenic and osteogenic differentiation of MSCs is studied on vertically aligned TiO(2) nanotubes of size 15 and 100 nm with and without immobilized bone morphogenetic protein-2 (BMP-2). Although BMP-2 coating stimulates both chondrogenic and osteogenic differentiation of MSCs, the response strongly depends on the surface nanoscale geometry of the BMP-2-coated nanotubes. Chondrogenic differentiation is strongly supported on 100 nm BMP-2-coated nanotubes, but not on 15 nm nanotubes, which induce spreading and de-differentiation of chondrocytes. A similar response is observed with primary chondrocytes, which maintain their chondrogenic phenotype on BMP-2-coated 100 nm nanotubes, but de-differentiate on 15 nm nanotubes. In contrast, osteogenic differentiation is greatly enhanced on 15 nm but not on 100 nm BMP-2-coated nanotubes as shown previously. Furthermore, covalent immobilization of BMP-2 rescues MSCs from apoptosis occurring on uncoated 100 nm TiO(2) nanotube surfaces. Thus, combined signals provided by BMP-2 immobilized to a defined lateral nanoscale spacing geometry seem to contain environmental cues that are able to modulate a lineage-specific decision of MSC differentiation and cell survival in a synergistic manner.

摘要

本研究旨在阐明纳米级形貌和生长因子提供的组合环境信号是否以协同或简单累加的方式控制间充质干细胞(MSCs)的细胞行为。研究了大小为 15nm 和 100nm 的垂直排列 TiO2 纳米管上 MSC 的软骨和成骨分化,这些纳米管有无固定的骨形态发生蛋白-2(BMP-2)。尽管 BMP-2 涂层刺激 MSC 的软骨和成骨分化,但这种反应强烈依赖于 BMP-2 涂层纳米管的表面纳米级几何形状。100nm 的 BMP-2 涂层纳米管强烈支持软骨分化,但 15nm 的纳米管则诱导软骨细胞的铺展和去分化。初级软骨细胞也观察到类似的反应,它们在 BMP-2 涂层的 100nm 纳米管上保持软骨细胞表型,但在 15nm 纳米管上则去分化。相反,如前所述,15nm 的 BMP-2 涂层纳米管极大地增强了成骨分化,但 100nm 的 BMP-2 涂层纳米管则没有。此外,BMP-2 的共价固定可挽救未涂层 100nm TiO2 纳米管表面上发生的 MSC 凋亡。因此,固定在特定横向纳米级间距几何形状上的 BMP-2 提供的组合信号似乎包含环境线索,能够以协同方式调节 MSC 分化和细胞存活的谱系特异性决定。

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