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周期性机械应变下生化微图案水凝胶涂层上的成肌细胞形态和组织。

Myoblast morphology and organization on biochemically micro-patterned hydrogel coatings under cyclic mechanical strain.

机构信息

Department of Mechanical Sciences and Engineering, University of Illinois at Urbana-Champaign, 1206 West Green Street, Urbana, IL 61801, USA.

出版信息

Biomaterials. 2010 Jan;31(2):250-8. doi: 10.1016/j.biomaterials.2009.09.047. Epub 2009 Sep 26.

Abstract

Mechanical forces and geometric constraints play critical roles in determining cell functionality and tissue development. Novel experimental methods are essential to explore the underlying biological mechanisms of cell response. We present a versatile method to culture cells on adhesive micro-patterned substrates while applying long-term cyclic tensile strain (CTS). A polydimethysiloxane (PDMS) mold is coated with a cell repulsive NCO-sP(EO-stat-PO) hydrogel which in turn is covalently patterned by fibronectin using micro-contact printing. This results in two-dimensional, highly selective cell-adhesive micro-patterns. The substrates allow application of CTS to adherent cells for more than 4 days under cell culture conditions without unspecific adhesion. The applicability of our system is demonstrated by studying the adaptive response of C2C12 skeletal myoblasts seeded on fibronectin lines with different orientations relative to the strain direction. After application of CTS (amplitude of 7%, frequency of 0.5 Hz) we find that actin fiber organization is dominantly controlled by CTS. Nuclei shape is predominantly affected by the constraint of the adhesive lines, resulting in significant elongation. Morphologically, myotube formation was incomplete after 4 days of culture, but actin striations were observed exclusively on the 45 degrees line patterns subjected to CTS, the direction of maximum shear strain.

摘要

机械力和几何约束在决定细胞功能和组织发育方面起着关键作用。新颖的实验方法对于探索细胞反应的潜在生物学机制至关重要。我们提出了一种通用的方法,可以在对细胞施加长期循环拉伸应变(CTS)的同时,在具有粘性的微图案化基底上培养细胞。聚二甲基硅氧烷(PDMS)模具涂覆有细胞排斥性 NCO-sP(EO-stat-PO)水凝胶,该水凝胶通过微接触印刷再用纤维连接蛋白进行共价图案化。这导致二维、高度选择性的细胞附着微图案。在细胞培养条件下,这些基底允许对附着的细胞施加 CTS 超过 4 天,而不会发生非特异性附着。我们的系统的适用性通过研究在纤维连接蛋白线(相对于应变方向具有不同取向)上接种 C2C12 成肌细胞的适应性反应来证明。施加 CTS(幅度为 7%,频率为 0.5 Hz)后,我们发现肌动蛋白纤维组织主要受 CTS 控制。细胞核形状主要受到粘性线的约束影响,导致显著的伸长。形态上,培养 4 天后肌管形成不完全,但仅在 45 度线图案上观察到 CTS 作用下的肌动蛋白条纹,这是最大剪切应变的方向。

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