Human maxillary tuberosity and jaw periosteum as sources of osteoprogenitor cells for tissue engineering

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007 Nov;104(5):618.e1-12. doi: 10.1016/j.tripleo.2007.02.022. Epub 2007 Jul 5.

Abstract

Objective: Bone tissue engineering is a promising approach for bone reconstruction in oral-maxillofacial surgery. This study investigates the suitability of oral skeletal tissues as convenient and accessible sources of osteogenic progenitors as an alternative to the iliac crest bone marrow.

Study design: Samples of maxilla tuberosity (MT) and maxillary and mandibular periosteum (MP) were obtained during routine oral surgery, and donor site morbidity was assessed using a "split-mouth" approach. Cells isolated from MT (bone marrow stromal cells; MT-BMSCs) and from MP (periosteal cells; M-PCs), were analyzed for clonogenicity, phenotype, expression of osteogenic markers, and ability to form bone in vivo.

Results: Both MT-BMSCs and M-PCs included clonogenic cells, showed comparable phenotypic profiles, and expressed early osteogenic markers. Most importantly, both cell populations formed bone upon ectopic in vivo transplantation.

Conclusion: MT-BMSCs and M-PCs behaved as osteoprogenitor cells in vitro and in vivo. MT and MP may be considered as suitable sources of cells for bone tissue engineering in humans.

Publication types

  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • ADP-ribosyl Cyclase / metabolism
  • Adult
  • Analysis of Variance
  • Animals
  • Antigens, CD / metabolism
  • Bone Marrow Cells / cytology*
  • Bone Regeneration
  • Cell Proliferation
  • Colony-Forming Units Assay / methods
  • Female
  • Flow Cytometry / methods
  • GPI-Linked Proteins
  • Humans
  • Male
  • Mandible / cytology*
  • Maxilla / cytology*
  • Mice
  • Periosteum / cytology*
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Tissue Engineering / methods*
  • Transcription Factors / analysis

Substances

  • Antigens, CD
  • GPI-Linked Proteins
  • Transcription Factors
  • ADP-ribosyl Cyclase
  • ADP-ribosyl cyclase 2