Directing lineage specification of human mesenchymal stem cells by decoupling electrical stimulation and physical patterning on unmodified graphene

被引:42
作者
Balikov, Daniel A. [1 ]
Fang, Brian [1 ,2 ]
Chun, Young Wook [1 ,3 ,5 ]
Crowder, Spencer W. [1 ,6 ]
Prasai, Dhiraj [2 ]
Lee, Jung Bok [1 ]
Bolotin, Kiril I. [2 ]
Sung, Hak-Joon [1 ,3 ,4 ]
机构
[1] Vanderbilt Univ, Dept Biomed Engn, Nashville, TN 37235 USA
[2] Vanderbilt Univ, Dept Phys & Astron, Nashville, TN 37235 USA
[3] Vanderbilt Univ, Med Ctr, Dept Med, Div Cardiovasc Med, Nashville, TN 37232 USA
[4] Yonsei Univ, Severance Biomed Sci Inst, Coll Med, Seoul, South Korea
[5] Emory Univ, Sch Med, Dept Med, Div Cardiol, Atlanta, GA USA
[6] Imperial Coll London, Dept Mat & Bioengn, London, England
基金
美国国家科学基金会;
关键词
MICROTUBULE-ASSOCIATED PROTEINS; EXTRACELLULAR-MATRIX; STROMAL CELLS; EXPRESSION; DIFFERENTIATION; REGENERATION; BONE; OSTEOPONTIN; OSTEOGENESIS; NEUROGENESIS;
D O I
10.1039/c6nr04400j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The organization and composition of the extracellular matrix (ECM) have been shown to impact the propagation of electrical signals in multiple tissue types. To date, many studies with electroactive biomaterial substrates have relied upon passive electrical stimulation of the ionic media to affect cell behavior. However, development of cell culture systems in which stimulation can be directly applied to the material - thereby isolating the signal to the cell-material interface and cell-cell contracts - would provide a more physiologically-relevant paradigm for investigating how electrical cues modulate lineage-specific stem cell differentiation. In the present study, we have employed unmodified, directly-stimulated, (un)patterned graphene as a cell culture substrate to investigate how extrinsic electrical cycling influences the differentiation of naive human mesenchymal stem cells (hMSCs) without the bias of exogenous biochemicals. We first demonstrated that cyclic stimulation does not deteriorate the cell culture media or result in cytotoxic pH, which are critical experiments for correct interpretation of changes in cell behavior. We then measured how the expression of osteogenic and neurogenic lineage-specific markers were altered simply by exposure to electrical stimulation and/or physical patterns. Expression of the early osteogenic transcription factor RUNX2 was increased by electrical stimulation on all graphene substrates, but the mature marker osteopontin was only modulated when stimulation was combined with physical patterns. In contrast, the expression of the neurogenic markers MAP2 and beta(3)-tubulin were enhanced in all electrical stimulation conditions, and were less responsive to the presence of patterns. These data indicate that specific combinations of non-biological inputs - material type, electrical stimulation, physical patterns - can regulate hMSC lineage specification. This study represents a substantial step in understanding how the interplay of electrophysical stimuli regulate stem cell behavior and helps to clarify the potential for graphene substrates in tissue engineering applications.
引用
收藏
页码:13730 / 13739
页数:10
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