Culturing on decellularized extracellular matrix enhances antioxidant properties of human umbilical cord-derived mesenchymal stem cells

被引:50
|
作者
Liu, Xiaozhen [1 ]
Zhou, Long [2 ,3 ]
Chen, Xi [2 ,3 ]
Liu, Tao
Pan, Guoqing [2 ,3 ]
Cui, Wenguo [2 ,3 ]
Li, Mao [2 ,3 ]
Luo, Zong-Ping [2 ,3 ]
Pei, Ming [4 ]
Yang, Huilin [2 ,3 ]
Gong, Yihong [1 ]
He, Fan [2 ,3 ]
机构
[1] Sun Yat Sen Univ, Sch Engn, Guangzhou 510006, Guangdong, Peoples R China
[2] Soochow Univ, Inst Orthopaed, 708 Renmin Rd, Suzhou 215007, Jiangsu, Peoples R China
[3] Soochow Univ, Affiliated Hosp 1, Dept Orthopaed, Suzhou 215006, Peoples R China
[4] W Virginia Univ, Dept Orthopaed, Stem Cell & Tissue Engn Lab, Morgantown, WV 26506 USA
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
Extracellular matrix; Mesenchymal stem cells; Antioxidative enzymes; Reactive oxygen species; Osteogenesis; OXIDATIVE STRESS; HYDROGEN-PEROXIDE; BONE-MARROW; EX-VIVO; DIFFERENTIATION; MELATONIN; SUPEROXIDE; PROLIFERATION; SENESCENCE; PROTECTS;
D O I
10.1016/j.msec.2015.12.090
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
Human umbilical cord-derived mesenchymal stem cells (UC-MSCs) have attracted great interest in clinical application because of their regenerative potential and their lack of ethical issues. Our previous studies showed that decellularized cell-deposited extracellular matrix (ECM) provided an in vivo-mimicking microenvironment for MSCs and facilitated in vitro cell expansion. This study was conducted to analyze the cellular response of UC-MSCs when culturing on the ECM, including reactive oxygen species (ROS), intracellular antioxidative enzymes, and the resistance to exogenous oxidative stress. After decellularization, the architecture of cell-deposited ECM was characterized as nanofibrous, collagen fibrils and the matrix components were identified as type I and III collagens, fibronectin, and laminin. Compared to tissue culture polystyrene (TCPS) plates, culturing on ECM yielded a 2-fold increase of UC-MSC proliferation and improved the percentage of cells in the S phase by 2.4 fold. The levels of intracellular ROS and hydrogen peroxide (H2O2) in ECM-cultured cells were reduced by 41.7% and 82.9%, respectively. More importantly, ECM-cultured UC-MSCs showed enhanced expression and activity of intracellular antioxidative enzymes such as superoxide dismutase and catalase, up-regulated expression of silent information regulator type 1, and suppressed phosphorylation of p38 mitogen-activated protein kinase. Furthermore, a continuous treatment with exogenous 100 mu M H2O2 dramatically inhibited osteogenic differentiation of UC-MSCs cultured on TCPS, but culturing on ECM retained the differentiation capacity for matrix mineralization and osteoblast-specific marker gene expression. Collectively, by providing sufficient cell amounts and enhancing antioxidant capacity, decellularized ECM can be a promising cell culture platform for in vitro expansion of UC-MSCs. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:437 / 448
页数:12
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