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Mesenchymal stem cells cultured on magnetic nanowire substrates

机译:在磁性纳米线基材上培养的间充质干细胞

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摘要

Stem cells have been shown to respond to extracellular mechanical stimuli by regulating their fate through the activation of specific signaling pathways. In this work, an array of iron nanowires (NWs) aligned perpendicularly to the surface was fabricated by pulsed electrodepositon in porous alumina templates followed by a partial removal of the alumina to reveal 2-3 mu m of the NWs. This resulted in alumina substrates with densely arranged NWs of 33 nm in diameter separated by 100 nm. The substrates were characterized by scanning electron microscopy (SEM) energy dispersive x-ray analysis and vibrating sample magnetometer. The NW array was then used as a platform for the culture of human mesenchymal stem cells (hMSCs). The cells were stained for the cell nucleus and actin filaments, as well as immunostained for the focal adhesion protein vinculin, and then observed by fluorescence microscopy in order to characterize their spreading behavior. Calcein AM/ethidium homodimer-1 staining allowed the determination of cell viability. The interface between the cells and the NWs was studied using SEM. Results showed that hMSCs underwent a re-organization of actin filaments that translated into a change from an elongated to a spherical cell shape. Actin filaments and vinculin accumulated in bundles, suggesting the attachment and formation of focal adhesion points of the cells on the NWs. Though the overall number of cells attached on the NWs was lower compared to the control, the attached cells maintained a high viability (>90%) for up to 6 d. Analysis of the interface between the NWs and the cells confirmed the re-organization of F-actin and revealed the adhesion points of the cells on the NWs. Additionally, a net of filopodia surrounded each cell, suggesting the probing of the array to find additional adhesion points. The cells maintained their round shape for up to 6 d of culture. Overall, the NW array is a promising nanostructured platform for studying and influencing hMSCs
机译:已经证明干细胞通过通过对特定信号通路的激活调节其命运来响应细胞外机械刺激。在这项工作中,通过多孔氧化铝模板中的脉冲电沉积件制造垂直于表面对齐的铁纳米线(NWS)的阵列,然后部分去除氧化铝以显示2-3μm。这导致氧化铝基材,其直径为33nm的浓密布置的NW,由100nm分开。通过扫描电子显微镜(SEM)能量分散X射线分析和振动样品磁力计,表征基材。然后将NW阵列用作人间充质干细胞培养的平台(HMSCs)。将细胞染色用于细胞核和肌动蛋白长丝,以及用于局灶性粘附蛋白vinculin的免疫染色,然后通过荧光显微镜观察,以表征其扩散行为。 Calcein AM /乙氢偶氮二聚体-1染色允许测定细胞活力。使用SEM研究细胞和NWS之间的界面。结果表明,HMSCs经历了转化为从伸长到球形细胞形状的变化的肌动蛋白长丝的重新组织。肌动蛋白长丝和vinculin积累在束中,表明NWS上细胞的局灶性粘附点的附着和形成。虽然与对照相比,在NW上附着在NWS上的细胞总数较低,但附着的细胞保持高可活力(> 90%),最多可达6天。对NWS和细胞之间的界面分析证实了F-Actin的重新组织,并揭示了NWS上细胞的粘附点。另外,围绕剥离的漏斗围绕着每个细胞,表明阵列探测以找到额外的粘合点。细胞保持其圆形,最多6天培养。总的来说,NW阵列是一个有前途的纳米结构平台,用于研究和影响HMSCs

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