Novel gene-activated matrix with embedded chitosan/plasmid DNA nanoparticles encoding PDGF for periodontal tissue engineering

被引:57
作者
Peng, Lin [1 ,2 ,3 ]
Cheng, Xiangrong [1 ,2 ]
Zhuo, Renxi [3 ]
Lan, Jing [4 ,5 ]
Wang, Yining [1 ,2 ]
Shi, Bin [1 ,2 ]
Li, Siqun [1 ,2 ]
机构
[1] Wuhan Univ, Key Lab Oral Biomed Engn Minist Educ, Dept Prosthodont, Sch Stomatol, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Hosp Stomatol, Wuhan 430072, Peoples R China
[3] Wuhan Univ, Dept Chem, Key Lab Biomed Polymers Minist Educ, Wuhan 430072, Peoples R China
[4] Shandong Univ, Dept Prosthodont, Sch Stomatol, Jinan 250100, Peoples R China
[5] Shandong Univ, Hosp Stomatol, Jinan 250100, Peoples R China
基金
中国国家自然科学基金;
关键词
gene-activated matrix; chitosan/collagen scaffold; platelet-derived growth factor; periodontal ligament cell; tissue engineering; IN-VITRO; PLASMID DNA; DELIVERY; SCAFFOLDS; FABRICATION; THERAPY; EXPRESSION; AGENT;
D O I
10.1002/jbm.a.32117
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Recently, much attention has been paid to tissue engineering and local gene delivery system in periodontal tissue regeneration. Gene-activated matrix (GAM) blends these two strategies, serving as a local bioreactor with therapeutic gene expression and providing a structural template to fill the lesion defects for cell adhesion, proliferation and synthesis of extracellular matrix (ECM). In this study, we designed a novel GAM with embedded chitosan/plasmid nanoparticles encoding platelet derived growth factor (PDGF) based on porous chitosan/collagen composite scaffold. The chitosan/collagen scaffold acted as three-dimensional carrier and chitosan nanoparticles condensed plasmid DNA. The plasmid DNA entrapped in the scaffolds showed a sustained and steady release over 6 weeks and could be effectively protected by chitosan nanoparticles. MTT assay demonstrated that periodontal ligament cells (PDLCs) cultured into the novel CAM achieved high proliferation. Luciferase reporter gene assay displayed that the novel GAM could express 1.07x10(4) LU/mg protein after 1 week and 8.97x10(3) LU/mg protein after 2 weeks. The histological results confirmed that PDLCs maintained a fibroblast figure and the periodontal connective tissue-like structure formed in the scaffolds after 2 weeks. Semi-quantitative immunohistochemical results suggested that PDGF protein expressed at a relatively high level after 2 weeks. From this study, it can be concluded that the novel GAM had potential in the application of periodontal tissue engineering. (C) 2008 Wiley Periodicals, Inc. J Biomed Mater Res 90A: 564-576, 2009
引用
收藏
页码:564 / 576
页数:13
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