Specific interactions between human fibroblasts and particular chondroitin sulfate molecules for wound healing

被引:66
作者
Zou, Xiao Hui [2 ]
Jiang, Yang Zi [1 ,3 ]
Zhang, Guo Rong [1 ,3 ]
Jin, Hang Mei [2 ]
Hieu, Nguyen Thi Minh [4 ]
Ouyang, Hong Wei [1 ,3 ]
机构
[1] Zhejiang Univ, Sch Med, Ctr Stem Cell & Tissue Engn, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Womens Hosp, Hangzhou 310058, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Dept Sports Med, Hangzhou 310058, Zhejiang, Peoples R China
[4] Natl Univ Singapore, Div Bioengn, Singapore 117548, Singapore
关键词
Chondroitin sulfate; Wound healing; Cell material interaction; Tissue engineering; HUMAN-ENDOTHELIAL CELLS; GROWTH-FACTOR; PROTEOGLYCANS; MATRICES; DIFFERENTIATION; EXPRESSION; MEMBRANE; FACTOR-2; LAMININ; LIGAND;
D O I
10.1016/j.actbio.2008.12.001
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
The chondroitin sulfates (CSs) constitute an important group of biomacromolecules in the extracellular matrix. However, limited information is available about their specific biological functions. This study aimed to define the interactions between cells and various types of CS. The effects of CSs on cellular activities and the cell cycle were evaluated using cell culture, RNA interference, real-time polymerase chain reaction, flow cytometry, wound healing and contraction models. The results showed that C-6-S promoted both cell proliferation and adhesion, while C-4-S promoted proliferation but inhibited adhesion. Moreover, knockdown of chondroitin inhibited cell proliferation and migration, as well as arresting cells in the G(2)/M phase. Also, both C-4-S and C-6-S promoted wound closure in a two-dimensional wound model, whereas only C-6-S inhibited wound contraction in a three-dimensional wound model. This study illustrates that the interaction between cells and different CSs are specific and sulfate-group-dependent. These findings provide useful information for better applications of CSs for wound healing. (c) 2009 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1588 / 1595
页数:8
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