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纳米结构特征的改变决定干细胞分化。

Altered nanofeature size dictates stem cell differentiation.

机构信息

INSERM, U1026, BioIngénierie Tissulaire, F-33076 Bordeaux, France.

出版信息

J Cell Sci. 2012 Mar 1;125(Pt 5):1217-24. doi: 10.1242/jcs.093229. Epub 2012 Feb 2.

Abstract

The differentiation of stem cells can be modulated by physical factors such as the micro- and nano-topography of the extracellular matrix. One important goal in stem cell research is to understand the concept that directs differentiation into a specific cell lineage in the nanoscale environment. Here, we demonstrate that such paths exist by controlling only the micro- and nano-topography of polymer surfaces. Altering the depth (on a nanometric scale) of micro-patterned surface structures allowed increased adhesion of human mesenchymal stem cells (hMSCs) with specific differentiation into osteoblasts, in the absence of osteogenic medium. Small (10 nm) depth patterns promoted cell adhesion without noticeable differentiation, whereas larger depth patterns (100 nm) elicited a collective cell organization, which induced selective differentiation into osteoblast-like cells. This latter response was dictated by stress through focal-adhesion-induced reorganization of F-actin filaments. The results have significant implications for understanding the architectural effects of the in vivo microenvironment and also for the therapeutic use of stem cells.

摘要

干细胞的分化可以通过物理因素来调节,例如细胞外基质的微观和纳米形貌。干细胞研究的一个重要目标是理解在纳米尺度环境中指导分化为特定细胞谱系的概念。在这里,我们通过仅控制聚合物表面的微观和纳米形貌来证明这种途径的存在。改变微图案表面结构的深度(纳米尺度)允许人骨髓间充质干细胞(hMSCs)增加附着,并且在没有成骨培养基的情况下特异性分化为成骨细胞。小(10nm)深度图案促进细胞附着而没有明显的分化,而较大的深度图案(100nm)引起细胞的集体组织,诱导成骨细胞样细胞的选择性分化。这种后者反应是通过由粘着斑诱导的 F-肌动蛋白丝的重排引起的力来调节的。这些结果对于理解体内微环境的结构效应具有重要意义,并且对于干细胞的治疗用途也具有重要意义。

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