Myoblast alignment and differentiation on cell culture substrates with microscale topography and model chemistries

被引:230
作者
Charest, Joseph L. [1 ]
Garcia, Andres J. [1 ]
King, William P. [1 ]
机构
[1] Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30329 USA
基金
美国国家科学基金会;
关键词
surface topography; surface chemistry; differentiation; myoblast; hot embossing; sarcomeric myosin;
D O I
10.1016/j.biomaterials.2007.01.020
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This paper analyzes the alignment and differentiation of myoblast cells adherent to surfaces having model chemistries and micro topographical patterns. The patterns strongly influenced cellular alignment but did not modulate expression of differentiation marker proteins in either primary or C2Cl2 myoblasts. Topographic patterns consisted of embossed ridges and grooves or arrays of holes, with feature sizes ranging from 5-75 mu m. The topographic surfaces were prepared with a uniform self-assembled monolayer that presented CH3 molecules for fibronectin adsorption. The myoblast cell models were cultured in differentiation conditions on the substrates. For both cell models, cells aligned to grooves, with groove width modulating orientation, and preferentially orientated parallel to rows of holes. None of the patterns significantly modulated cell density or differentiation as examined through sarcomeric myosin and acetylcholine receptor expression. The results indicate that for the specific configuration examined, microscale topography modulates myoblast alignment, but does not have significant impact on cell density or differentiation. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2202 / 2210
页数:9
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