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

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 GAM achieved high proliferation. Luciferase reporter gene assay displayed that the novel GAM could express 1.07 x 10(4) LU/mg protein after 1 week and 8.97 x 10(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.

[1]  J Bonadio,et al.  Tissue engineering via local gene delivery: update and future prospects for enhancing the technology. , 2000, Advanced drug delivery reviews.

[2]  R. Mumper,et al.  Chitosan-based nanoparticles for topical genetic immunization. , 2001, Journal of controlled release : official journal of the Controlled Release Society.

[3]  Tao Wang,et al.  Chitosan nanoparticle as protein delivery carrier--systematic examination of fabrication conditions for efficient loading and release. , 2007, Colloids and surfaces. B, Biointerfaces.

[4]  Lonnie D Shea,et al.  Controlled release systems for DNA delivery. , 2004, Molecular therapy : the journal of the American Society of Gene Therapy.

[5]  A. Kantarcı,et al.  Resolution of Inflammation in Periodontitis. , 2005, Journal of periodontology.

[6]  Zhi Ding,et al.  Porous chitosan-gelatin scaffold containing plasmid DNA encoding transforming growth factor-beta1 for chondrocytes proliferation. , 2006, Biomaterials.

[7]  J. Mao,et al.  Study of novel chitosan-gelatin artificial skin in vitro. , 2003, Journal of biomedical materials research. Part A.

[8]  R. Kao,et al.  Tissue engineering for periodontal regeneration. , 2005, Journal of the California Dental Association.

[9]  M. Chiba,et al.  Local OPG Gene Transfer to Periodontal Tissue Inhibits Orthodontic Tooth Movement , 2004, Journal of dental research.

[10]  W. Ahn,et al.  The use of chitosan as a condensing agent to enhance emulsion-mediated gene transfer. , 2005, Biomaterials.

[11]  Jiawei Wang,et al.  Preparation and Evaluation of Porous Chitosan/Collagen Scaffolds for Periodontal Tissue Engineering , 2006 .

[12]  Q. Jin,et al.  Gene therapeutics for periodontal regenerative medicine. , 2006, Dental clinics of North America.

[13]  Y. Okahata,et al.  In vitro gene delivery mediated by chitosan. effect of pH, serum, and molecular mass of chitosan on the transfection efficiency. , 2001, Biomaterials.

[14]  Hassan Adwan,et al.  Delivery and expression of pDNA embedded in collagen matrices. , 2004, Journal of controlled release : official journal of the Controlled Release Society.

[15]  J. Fernandes,et al.  Chitosan-DNA nanoparticles as non-viral vectors in gene therapy: strategies to improve transfection efficacy. , 2004, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[16]  L. Chandler,et al.  Matrix‐enabled gene transfer for cutaneous wound repair , 2000, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[17]  William V Giannobile,et al.  Engineering of tooth-supporting structures by delivery of PDGF gene therapy vectors. , 2004, Molecular therapy : the journal of the American Society of Gene Therapy.

[18]  Y. Tabata,et al.  Efficacy and cytotoxicity of cationic-agent-mediated nonviral gene transfer into osteoblasts. , 2004, Journal of biomedical materials research. Part A.

[19]  M. Torbenson,et al.  Chitosan-DNA nanoparticles delivered by intrabiliary infusion enhance liver-targeted gene delivery , 2006, International journal of nanomedicine.

[20]  Shubiao Zhang,et al.  Toxicity of cationic lipids and cationic polymers in gene delivery. , 2006, Journal of controlled release : official journal of the Controlled Release Society.

[21]  David J Mooney,et al.  Sustained delivery of plasmid DNA from polymeric scaffolds for tissue engineering. , 2006, Advanced drug delivery reviews.

[22]  R. Lockey,et al.  Nanoparticle-mediated gene delivery: state of the art , 2004, Expert opinion on biological therapy.

[23]  T. Bettinger,et al.  Chitosan-Based Vector/DNA Complexes for Gene Delivery: Biophysical Characteristics and Transfection Ability , 1998, Pharmaceutical Research.

[24]  B. Karthikeyan,et al.  Gene therapy in periodontics: a review and future implications. , 2006, The journal of contemporary dental practice.

[25]  Y Wang,et al.  Chitosan-DNA nanoparticles as gene carriers: synthesis, characterization and transfection efficiency. , 2001, Journal of controlled release : official journal of the Controlled Release Society.

[26]  Yan Li,et al.  Chitosan nanoparticle as gene therapy vector via gastrointestinal mucosa administration: results of an in vitro and in vivo study. , 2007, Life sciences.

[27]  D. Steinberg,et al.  Soluble sustained release gene delivery system. , 2006, Journal of biomedical materials research. Part A.

[28]  David J Mooney,et al.  Fabrication and in vitro testing of polymeric delivery system for condensed DNA. , 2003, Journal of biomedical materials research. Part A.

[29]  K. Leong,et al.  Chitosan nanoparticles for oral drug and gene delivery , 2006, International journal of nanomedicine.

[30]  Chi-Hwa Wang,et al.  Fabrication and characterization of PLGA/HAp composite scaffolds for delivery of BMP-2 plasmid DNA. , 2007, Journal of controlled release : official journal of the Controlled Release Society.

[31]  J. Hubbell,et al.  Non-viral gene delivery for local and controlled DNA release. , 2005, Journal of controlled release : official journal of the Controlled Release Society.

[32]  L. Shea,et al.  Nerve growth factor expression by PLG-mediated lipofection. , 2006, Biomaterials.

[33]  C. Plank,et al.  Nonviral vector loaded collagen sponges for sustained gene delivery in vitro and in vivo , 2002, The journal of gene medicine.

[34]  Jeffrey Bonadio,et al.  Localized, direct plasmid gene delivery in vivo: prolonged therapy results in reproducible tissue regeneration , 1999, Nature Medicine.

[35]  Jae‐Hyung Jang,et al.  Surface adsorption of DNA to tissue engineering scaffolds for efficient gene delivery. , 2006, Journal of biomedical materials research. Part A.

[36]  K. Ohya,et al.  Bone regeneration by modified gene-activated matrix: effectiveness in segmental tibial defects in rats. , 2006, Tissue engineering.