Insulin-like growth factor 1 can promote the osteogenic differentiation and osteogenesis of stem cells from apical papilla

Stem Cell Res. 2012 May;8(3):346-56. doi: 10.1016/j.scr.2011.12.005. Epub 2011 Dec 21.

Abstract

Insulin-like growth factor 1 (IGF-1) plays an important role in the regulation of tooth root development, and stem cells from apical papilla (SCAPs) are responsible for the formation of root pulp and dentin. To date, it remains unclear whether IGF-1 can regulate the function of SCAPs. In this study, SCAPs were isolated and purified from human immature root apex, and stimulated by 100 ng/mL exogenous IGF-1. The effects of IGF-1 on the proliferation and differentiation of SCAPs were subsequently investigated. IGF-1 treated SCAPs presented the morphological and ultrastructural changes. Cell proliferation, alkaline phosphatase (ALP) activity and mineralization capacity of SCAPs were increased by IGF-1. Western blot and quantitative RT-PCR analyses further demonstrated that the expression of osteogenic-related proteins and genes (e.g., alkaline phosphatase, runt-related transcription factor 2, osterix, and osteocalcin) was significantly up-regulated in IGF-1 treated SCAPs, whereas the expression of odontoblast-specific markers (e.g., dentin sialoprotein and dentin sialophosphoprotein) was down-regulated by IGF-1. In vivo results revealed that IGF-1 treated SCAPs mostly gave birth to bone-like tissues while untreated SCAPs mainly generated dentin-pulp complex-like structures after transplantation. The present study revealed that IGF-1 can promote the osteogenic differentiation and osteogenesis capacity of SCAPs, but weaken their odontogenic differentiation and dentinogenesis capability, indicating that IGF-1 treated SCAPs can be used as a potential candidate for bone tissue engineering.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Alkaline Phosphatase / genetics
  • Alkaline Phosphatase / metabolism
  • Cell Differentiation / drug effects*
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Core Binding Factor Alpha 1 Subunit / genetics
  • Core Binding Factor Alpha 1 Subunit / metabolism
  • Dental Papilla / cytology*
  • Dental Papilla / pathology
  • Extracellular Matrix Proteins / genetics
  • Extracellular Matrix Proteins / metabolism
  • Humans
  • Immunohistochemistry
  • Insulin-Like Growth Factor I / pharmacology*
  • Osteocalcin / genetics
  • Osteocalcin / metabolism
  • Osteogenesis / drug effects*
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • Sialoglycoproteins / genetics
  • Sialoglycoproteins / metabolism
  • Sp7 Transcription Factor
  • Stem Cells / cytology
  • Stem Cells / drug effects*
  • Stem Cells / ultrastructure
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Young Adult

Substances

  • Core Binding Factor Alpha 1 Subunit
  • Extracellular Matrix Proteins
  • Phosphoproteins
  • RUNX2 protein, human
  • Sialoglycoproteins
  • Sp7 Transcription Factor
  • SP7 protein, human
  • Transcription Factors
  • dentin sialophosphoprotein
  • Osteocalcin
  • Insulin-Like Growth Factor I
  • Alkaline Phosphatase