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纳米图案化黏附、可拉伸水凝胶控制配体间距,调节细胞铺展和迁移。

Nanopatterned Adhesive, Stretchable Hydrogel to Control Ligand Spacing and Regulate Cell Spreading and Migration.

机构信息

Department of Cellular Biophysics, Max Planck Institute for Medical Research, Heidelberg, and Laboratory of Biophysical Chemistry, University of Heidelberg , Jahnstraße 29, 69120 Heidelberg, Germany.

College of Polymer Science and Engineering, State Key Laboratory of Polymer Materials and Engineering, Sichuan University , Chengdu 610065, China.

出版信息

ACS Nano. 2017 Aug 22;11(8):8282-8291. doi: 10.1021/acsnano.7b03449. Epub 2017 Jul 20.

Abstract

Spatial molecular patterning enables the regulation of adhesion receptor clustering and can thus play a pivotal role in multiple biological activities such as cell adhesion, viability, proliferation, and differentiation. A wide range of nanopatterned, adhesive interfaces have been designed to decipher the essence of molecular-scale interactions between cells and the adhesive interface. Although an interligand spacing of less than 70 nm is a proven prerequisite for the formation of stable focal adhesions, there is a paucity of data concerning how cells behave on substrates featuring heterogeneous adhesiveness. In this study, a stretchable hydrogel functionalized with a quasi-hexagonally arranged nanoarray was stretched along one direction, resulting in ligands periodically arranged in a pattern resembling a centered rectangular lattice with an interligand spacing smaller than 70 nm in one direction and greater than 70 nm in the orthogonal direction. This substrate was utilized to modulate interligand spacing and investigate cell adhesion and migration. An interligand spacing larger than 70 nm-even in just one direction-prevented the establishment of stable focal adhesions. The stretched interface promoted dynamic remodeling at cell contacts, resulting in higher cellular mobility. Our nanopatterned stretchable hydrogel permits reversible control over cell adhesion and migration on nanopatterned ligand interfaces.

摘要

空间分子模式化可实现对粘附受体聚集的调控,从而在多种生物学活动中发挥关键作用,如细胞黏附、存活、增殖和分化。人们设计了广泛的纳米图案化、粘附界面,以破解细胞与粘附界面之间分子尺度相互作用的本质。尽管小于 70nm 的配体间隔是形成稳定粘着斑的已有前提,但关于细胞在具有异质性粘附力的基底上的行为的信息却很少。在这项研究中,一种具有准六边形排列纳米阵列的可拉伸水凝胶沿一个方向拉伸,导致配体以类似于中心矩形晶格的图案周期性排列,在一个方向上的配体间隔小于 70nm,而在正交方向上大于 70nm。该基底用于调节配体间隔并研究细胞黏附和迁移。大于 70nm 的配体间隔(即使只有一个方向)阻止了稳定粘着斑的建立。拉伸界面促进了细胞接触处的动态重塑,从而提高了细胞迁移率。我们的纳米图案化可拉伸水凝胶可在纳米图案化配体界面上实现对细胞黏附和迁移的可逆控制。

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