Chemical modification of extracellular matrix by cold atmospheric plasma-generated reactive species affects chondrogenesis and bone formation

被引:25
|
作者
Eisenhauer, Peter [1 ]
Chernets, Natalie [1 ]
Song, You [1 ]
Dobrynin, Danil [2 ]
Pleshko, Nancy [3 ]
Steinbeck, Marla J. [4 ]
Freeman, Theresa A. [1 ,2 ]
机构
[1] Thomas Jefferson Univ, Dept Orthopaed Surg, Curtis Bldg,Room 501,1015 Walnut St, Philadelphia, PA 19107 USA
[2] Drexel Univ, Drexel Plasma Inst, Philadelphia, PA 19104 USA
[3] Temple Univ, Dept Bioengn, Philadelphia, PA 19122 USA
[4] Drexel Univ, Sch Biomed Engn Sci & Hlth Syst, Philadelphia, PA 19104 USA
关键词
bone; FTIR; plasma; matrigel; chondrogenesis; endochondral ossification; DIELECTRIC BARRIER DISCHARGE; GROWTH;
D O I
10.1002/term.2224
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The goal of this study was to investigate whether cold plasma generated by dielectric barrier discharge (DBD) modifies extracellular matrices (ECM) to influence chondrogenesis and endochondral ossification. Replacement of cartilage by bone during endochondral ossification is essential in fetal skeletal development, bone growth and fracture healing. Regulation of this process by the ECM occurs through matrix remodelling, involving a variety of cell attachment molecules and growth factors, which influence cell morphology and protein expression. The commercially available ECM, Matrigel, was treated with microsecond or nanosecond pulsed (mu sp or nsp, respectively) DBD frequencies conditions at the equivalent frequencies (1 kHz) or power (similar to 1 W). Recombinant human bone morphogenetic protein-2 was added and the mixture subcutaneously injected into mice to simulate ectopic endochondral ossification. Two weeks later, the masses were extracted and analysed by microcomputed tomography. A significant increase in bone formation was observed in Matrigel treated with mu sp DBD compared with control, while a significant decrease in bone formation was observed for both nsp treatments. Histological and immunohistochemical analysis showed Matrigel treated with mu sp plasma increased the number of invading cells, the amount of vascular endothelial growth factor and chondrogenesis while the opposite was true for Matrigel treated with nsp plasma. In support of the in vivo Matrigel study, 10 T1/2 cells cultured in vitro on mu sp DBD-treated type I collagen showed increased expression of adhesion proteins and activation of survival pathways, which decreased with nsp plasma treatments. These results indicate DBD modification of ECM can influence cellular behaviours to accelerate or inhibit chondrogenesis and endochondral ossification. Copyright (C) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:772 / 782
页数:11
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