Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/106290
Title: Insights into the role of focal adhesion modulation in myogenic differentiation of human mesenchymal stem cells
Authors: Yu, Haiyang
Lui, Yuan Siang
Xiong, Sijing
Leong, Wen Shing
Wen, Feng
Nurkahfianto, Himawan
Rana, Sravendra
Leong, David Tai
Ng, Kee Woei
Tan, Lay Poh
Keywords: DRNTU::Engineering::Materials::Biomaterials
Issue Date: 2013
Source: Yu, H., Lui, Y. S., Xiong, S., Leong, W. S., Wen, F., Nurkahfianto, H., et al. (2013). Insights into the role of focal adhesion modulation in myogenic differentiation of human mesenchymal stem cells. Stem cells and development, 22(1), 136-147.
Series/Report no.: Stem cells and development
Abstract: We report the establishment of a novel platform to induce myogenic differentiation of human mesenchymal stem cells (hMSCs) via focal adhesion (FA) modulation, giving insights into the role of FA on stem cell differentiation. Micropatterning of collagen type I on a polyacrylamide gel with a stiffness of 10.2 kPa efficiently modulated elongated FA. This elongated FA profile preferentially recruited the β3 integrin cluster and induced specific myogenic differentiation at both transcription and translation levels with expression of myosin heavy chain and α-sarcomeric actin. This was initiated with elongation of FA complexes that triggered the RhoA downstream signaling toward a myogenic lineage commitment. This study also illustrates how one could partially control myogenic differentiation outcomes of similar-shaped hMSCs by modulating FA morphology and distribution. This technology increases our toolkit choice for controlled differentiation in muscle engineering.
URI: https://hdl.handle.net/10356/106290
http://hdl.handle.net/10220/23990
ISSN: 1547-3287
DOI: 10.1089/scd.2012.0160
Rights: © 2013 Mary Ann Liebert, Inc. This paper was published in Stem Cells and Development and is made available as an electronic reprint (preprint) with permission of Mary Ann Liebert, Inc. The paper can be found at the following official DOI: http://dx.doi.org/10.1089/scd.2012.0160.  One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles

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