Electrically Stimulated Adipose Stem Cells on Polypyrrole-Coated Scaffolds for Smooth Muscle Tissue Engineering

被引:0
|
作者
Miina Björninen
Kerry Gilmore
Jani Pelto
Riitta Seppänen-Kaijansinkko
Minna Kellomäki
Susanna Miettinen
Gordon Wallace
Dirk Grijpma
Suvi Haimi
机构
[1] University of Wollongong,ARC Centre of Excellence for Electromaterials Science, Intelligent Polymer Research Institute, AIIM Facility, Innovation Campus
[2] BioMediTech,Adult Stem Cells
[3] University of Tampere,Department of Oral and Maxillofacial Sciences, Clinicum, Faculty of Medicine
[4] VTT Technical Research Centre of Finland,Department of Oral and Maxillofacial Diseases, Head and Neck Center, Helsinki University Hospital, Institute of Dentistry
[5] University of Helsinki,Biomaterials and Tissue Engineering Group, Department of Electronics and Communications Engineering
[6] University of Helsinki,Science Center
[7] Tampere University of Technology,MIRA Institute for Biomedical Technology and Technical Medicine, Department of Biomaterials Science and Technology
[8] BioMediTech,Department of Biomedical Engineering
[9] Tampere University Hospital,undefined
[10] University of Twente,undefined
[11] University of Groningen,undefined
[12] University Medical Center Groningen,undefined
来源
关键词
Mesenchymal stem cells; Poly (trimethylene carbonate); Conductive polymers; Physical stimulation; Vascular tissue engineering;
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摘要
We investigated the use of polypyrrole (PPy)-coated polymer scaffolds and electrical stimulation (ES) to differentiate adipose stem cells (ASCs) towards smooth muscle cells (SMCs). Since tissue engineering lacks robust and reusable 3D ES devices we developed a device that can deliver ES in a reliable, repeatable, and cost-efficient way in a 3D environment. Long pulse (1 ms) or short pulse (0.25 ms) biphasic electric current at a frequency of 10 Hz was applied to ASCs to study the effects of ES on ASC viability and differentiation towards SMCs on the PPy-coated scaffolds. PPy-coated scaffolds promoted proliferation and induced stronger calponin, myosin heavy chain (MHC) and smooth muscle actin (SMA) expression in ASCs compared to uncoated scaffolds. ES with 1 ms pulse width increased the number of viable cells by day 7 compared to controls and remained at similar levels to controls by day 14, whereas shorter pulses significantly decreased viability compared to the other groups. Both ES protocols supported smooth muscle expression markers. Our results indicate that electrical stimulation on PPy-coated scaffolds applied through the novel 3D ES device is a valid approach for vascular smooth muscle tissue engineering.
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页码:1015 / 1026
页数:11
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