Nano-sized calcium phosphate particles for periodontal gene therapy

J Periodontol. 2013 Jan;84(1):117-25. doi: 10.1902/jop.2012.120012. Epub 2012 Mar 13.

Abstract

Background: Growth factors such as platelet-derived growth factor (PDGF) have significantly enhanced periodontal therapy outcomes with a high degree of variability, mostly due to the lack of continual supply for a required period of time. One method to overcome this barrier is gene therapy. The aim of this in vitro study is to evaluate PDGF-B gene delivery in fibroblasts using nano-sized calcium phosphate particles (NCaPP) as vectors.

Methods: NCaPP incorporating green fluorescent protein (NCaPP-GFP) and PDGF-B (NCaPP-PDGF-B) plasmids were synthesized using an established precipitation system and characterized using transmission electron microscopy and 1.2% agarose gel electrophoresis. Biocompatibility and transfection of the nanoplexes in fibroblasts were evaluated using cytotoxicity assay and florescence microscopy, respectively. Polymerase chain reaction and enzyme-linked immunosorbent assay were performed to evaluate PDGF-B transfection after different time points of treatments, and the functionality of PDGF-B transfection was evaluated using the cell proliferation assay.

Results: Synthesized NCaPP nanoplexes incorporating the genes of GFP and PDGF-B were spherical in shape and measured about 30 to 50 nm in diameter. Gel electrophoresis confirmed DNA incorporation and stability within the nanoplexes, and 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium reagent assay demonstrated their biocompatibility in fibroblasts. In vitro transfection studies revealed a higher and longer lasting transfection after NCaPP-PDGF-B treatment, which lasted up to 96 hours. Significantly enhanced fibroblast proliferation observed in NCaPP-PDGF-B-treated cells confirmed the functionality of these nanoplexes.

Conclusion: NCaPP demonstrated higher levels of biocompatibility and efficiently transfected PDGF plasmids into fibroblasts under described in vitro conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biocompatible Materials / chemical synthesis
  • Calcium Phosphates* / chemical synthesis
  • Calcium Phosphates* / chemistry
  • Cell Culture Techniques
  • Cell Proliferation
  • Cell Survival
  • Gene Expression Regulation / genetics
  • Genetic Therapy / methods*
  • Genetic Vectors* / chemical synthesis
  • Green Fluorescent Proteins
  • Luminescent Agents
  • Mice
  • NIH 3T3 Cells
  • Nanoparticles* / chemistry
  • Periodontal Diseases / therapy*
  • Plasmids / chemical synthesis
  • Proto-Oncogene Proteins c-sis / genetics*
  • Tetrazolium Salts
  • Thiazoles
  • Transfection / methods

Substances

  • Biocompatible Materials
  • Calcium Phosphates
  • Luminescent Agents
  • Proto-Oncogene Proteins c-sis
  • Tetrazolium Salts
  • Thiazoles
  • 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium
  • Green Fluorescent Proteins