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利用纳米拓扑结构研究成纤维细胞中的机械转导——方法与展望。

Use of nanotopography to study mechanotransduction in fibroblasts--methods and perspectives.

作者信息

Dalby Matthew J, Riehle Mathis O, Sutherland Duncan S, Agheli Hossein, Curtis Adam S G

机构信息

Centre for Cell Engineering, Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow, UK.

出版信息

Eur J Cell Biol. 2004 May;83(4):159-69. doi: 10.1078/0171-9335-00369.

Abstract

The environment around a cell during in vitro culture is unlikely to mimic those in vivo. Preliminary experiments with nanotopography have shown that nanoscale features can strongly influence cell morphology, adhesion, proliferation and gene regulation, but the mechanisms mediating this cell response remain unclear. In this perspective article, we attempt to illustrate that a possible mechanism is direct transmittal of forces encountered by cells during spreading to the nucleus via the cytoskeleton. We further try to illustrate that this 'self-induced' mechanotransduction may alter gene expression by changing interphase chromosome positioning. Whilst the observations described here to show how we think nanotopography can be developed as a tool to look at mechanotransduction are preliminary, we feel they indicate that topography may give cell biologists a non-invasive tool with which to investigate in vitro cellular mechanisms.

摘要

体外培养过程中细胞周围的环境不太可能模拟体内环境。纳米拓扑学的初步实验表明,纳米级特征可强烈影响细胞形态、黏附、增殖和基因调控,但介导这种细胞反应的机制仍不清楚。在这篇观点文章中,我们试图阐明一种可能的机制是,细胞铺展过程中遇到的力通过细胞骨架直接传递至细胞核。我们还试图阐明,这种“自我诱导”的机械转导可能通过改变间期染色体定位来改变基因表达。虽然此处描述的观察结果表明我们认为纳米拓扑学可如何发展成为一种研究机械转导的工具,但这些结果尚属初步,不过我们觉得它们表明拓扑学可能为细胞生物学家提供一种非侵入性工具,用以研究体外细胞机制。

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