Differential Regulation of Extracellular Matrix Components Using Different Vitamin C Derivatives in Mono- and Coculture Systems

被引:7
|
作者
Zhang, Xiaoqing [1 ]
Battiston, Kyle G. [3 ]
Simmons, Craig A. [1 ,2 ,3 ]
Santerre, J. Paul [1 ,3 ]
机构
[1] Univ Toronto, Translat Biol & Engn Program, Ted Rogers Ctr Heart Res, Inst Biomat & Biomed Engn, 661 Univ Ave,14th Floor, Toronto, ON M5G 1M1, Canada
[2] Univ Toronto, Dept Mech & Ind Engn, 5 Kings Coll Rd, Toronto, ON M5S 3G8, Canada
[3] Univ Toronto, Fac Dent, 124 Edward St, Toronto, ON M5G 1G6, Canada
来源
ACS BIOMATERIALS SCIENCE & ENGINEERING | 2018年 / 4卷 / 11期
基金
加拿大健康研究院;
关键词
tissue engineering; biodegradable polyurethane; ascorbic acid; sodium ascorbate; vascular smooth muscle cells; monocytes; SMOOTH-MUSCLE-CELL; ASCORBIC-ACID; IN-VITRO; POLYURETHANE SCAFFOLD; MOLECULAR REGULATION; COLLAGEN-SYNTHESIS; SODIUM ASCORBATE; GROWTH-FACTOR; EXPRESSION; PROLIFERATION;
D O I
10.1021/acsbiomaterials.7b00389
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Vascular tissue engineering strategies using cell-seeded scaffolds require uniformly distributed vascular cells and sufficient extracellular matrix (ECM) production. However, acquiring sufficient ECM deposition on synthetic biomaterial scaffolds during the in vitro culture period prior to tissue implantation still remains challenging for vascular constructs. Two forms of vitamin C derivatives, ascorbic acid (AA) and sodium ascorbate (SA), are commonly supplemented in cell culture to promote ECM accumulation. However, the literature often refers to AA and SA interchangeably, and their differential effects on cell growth and ECM molecule (glycosaminoglycan, collagen, elastin) accumulation have never been reported when used in monoculture or coculture systems developed with synthetic three-dimensional (3D) scaffolds. In this study, it was found that 200 mu M AA stimulated an increase in cell number, whereas SA (SO, 100, and 200 mu M) supported more calponin expression (immunostaining) and higher ECM accumulation from vascular smooth muscle cells (VSMCs) after 1 week in the degradable polar hydrophobic ionic polyurethane scaffold. The influence of AA and SA on ECM deposition was also studied in VSMC-monocyte cocultures to replicate some aspects of a wound healing environment in vitro and compared to their effects in respective VSMC monocultures after 4 weeks. Although 100 mu M SA promoted ECM deposition in coculture, the condition of 100 mu M AA + 100 mu M SA was more effective toward enhancing ECM accumulation in VSMC monoculture after 4 weeks. The results demonstrated that AA and SA are not interchangeable, and the different effects of AA and/or SA on ECM deposition were both culture system (co- vs monoculture) and culture period (1 vs 4 week) dependent. This study provides further insight into practical vascular tissue engineering strategies when using 3D synthetic biomaterial-based constructs.
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页码:3768 / 3778
页数:21
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