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用于细胞生物学的分子工程表面:从静态表面到动态表面

Molecularly engineered surfaces for cell biology: from static to dynamic surfaces.

作者信息

Gooding J Justin, Parker Stephen G, Lu Yong, Gaus Katharina

机构信息

The Australian Centre for NanoMedicine, ‡School of Chemistry, and §Centre for Vascular Research, The University of New South Wales , Sydney 2052, Australia.

出版信息

Langmuir. 2014 Apr 1;30(12):3290-302. doi: 10.1021/la4037919. Epub 2013 Nov 22.

Abstract

Surfaces with a well-defined presentation of ligands for receptors on the cell membrane can serve as models of the extracellular matrix for studying cell adhesion or as model cell surfaces for exploring cell-cell contacts. Because such surfaces can provide exquisite control over, for example, the density of these ligands or when the ligands are presented to the cell, they provide a very precise strategy for understanding the mechanisms by which cells respond to external adhesive cues. In the present feature article, we present an overview of the basic biology of cell adhesion before discussing surfaces that have a static presentation of immobile ligands. We outline the biological information that such surfaces have given us, before progressing to recently developed switchable surfaces and surfaces that mimic the lipid bilayer, having adhesive ligands that can move around the membrane and be remodeled by the cell. Finally, the feature article closes with some of the biological information that these new types of surfaces could provide.

摘要

细胞膜上具有明确定义的受体配体呈现的表面,可作为研究细胞黏附的细胞外基质模型,或作为探索细胞间接触的模型细胞表面。因为这样的表面能够对这些配体的密度或配体何时呈现给细胞等方面进行精确控制,所以它们为理解细胞对外部黏附信号的响应机制提供了一种非常精确的策略。在本篇专题文章中,我们在讨论具有固定不动配体静态呈现的表面之前,先对细胞黏附的基础生物学进行概述。在介绍最近开发的可切换表面和模拟脂质双层的表面(其具有可在膜周围移动并可被细胞重塑的黏附配体)之前,我们概述了此类表面所提供给我们的生物学信息。最后,这篇专题文章以这些新型表面可能提供的一些生物学信息作为结尾。

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