Hypoxia enhances colony formation and proliferation but inhibits differentiation of human dental pulp cells

Arch Oral Biol. 2010 Sep;55(9):648-54. doi: 10.1016/j.archoralbio.2010.06.005. Epub 2010 Jul 13.

Abstract

The hypoxia condition was expected to be suitable for the establishment and maintenance of human dental pulp cells (hDPCs), because they reside in a low-oxygen environment in vivo. Therefore, we presently examined the effects of hypoxia on the proliferation and differentiation of hDPCs in vitro. hDPCs grown under 3% O(2) showed a significantly higher proliferation rate than those under 21% O(2). Then, we prepared hypoxic cultures of hDPCs from older patients' teeth having inflammation and succeeded in recovering and expanding a small number of hDPCs. These cells were confirmed to have capability for osteo/odontogenic differentiation. Hypoxia suppressed the osteo/odontogenic differentiation of hDPCs in vitro and increased the number of cells expressing STRO-1, an early mesenchymal stem cell marker. This simple method will increase the possibility to obtain living hDPCs from damaged and/or aged tissues, from which it is ordinarily difficult to isolate living stem cells with differentiation capability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult Stem Cells / cytology*
  • Adult Stem Cells / metabolism
  • Aged
  • Antigens, Surface / biosynthesis
  • Cell Culture Techniques
  • Cell Differentiation
  • Cell Proliferation
  • Cells, Cultured
  • Dental Pulp / cytology*
  • Dental Pulp / metabolism
  • Epithelial Cells / cytology*
  • Epithelial Cells / metabolism
  • Extracellular Matrix Proteins / biosynthesis
  • Flow Cytometry
  • Humans
  • Hypoxia / metabolism
  • Hypoxia / pathology*
  • Mesenchymal Stem Cell Transplantation
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / metabolism
  • Middle Aged
  • Osteocalcin / biosynthesis
  • Phosphoproteins / biosynthesis
  • Polymerase Chain Reaction
  • Sialoglycoproteins / biosynthesis

Substances

  • Antigens, Surface
  • DMP1 protein, human
  • Extracellular Matrix Proteins
  • Phosphoproteins
  • STRO-1 antigen, human
  • Sialoglycoproteins
  • dentin sialophosphoprotein
  • Osteocalcin