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A computer-designed scaffold for bone regeneration within cranial defect using human dental pulp stem cells

  • Doo Yeon Kwon
  • , Jin Seon Kwon
  • , Seung Hun Park
  • , Ji Hun Park
  • , So Hee Jang
  • , Xiang Yun Yin
  • , Jeong Ho Yun
  • , Jae Ho Kim
  • , Byoung Hyun Min
  • , Jun Hee Lee
  • , Wan Doo Kim
  • , Moon Suk Kim*
  • *Corresponding author for this work
  • Ajou University
  • Korea Institute of Machinery and Materials
  • Inha University

Research output: Contribution to journalJournal articlepeer-review

Abstract

A computer-designed, solvent-free scaffold offer several potential advantages such as ease of customized manufacture and in vivo safety. In this work, we firstly used a computer-designed, solvent-free scaffold and human dental pulp stem cells (hDPSCs) to regenerate neo-bone within cranial bone defects. The hDPSCs expressed mesenchymal stem cell markers and served as an abundant source of stem cells with a high proliferation rate. In addition, hDPSCs showed a phenotype of differentiated osteoblasts in the presence of osteogenic factors (OF). We used solid freeform fabrication (SFF) with biodegradable polyesters (MPEG-(PLLA-co-PGA-co-PCL) (PLGC)) to fabricate a computer-designed scaffold. The SFF technology gave quick and reproducible results. To assess bone tissue engineering in vivo, the computer-designed, circular PLGC scaffold was implanted into a full-thickness cranial bone defect and monitored by micro-computed tomography (CT) and histology of the in vivo tissue-engineered bone. Neo-bone formation of more than 50% in both micro-CT and histology tests was observed at only PLGC scaffold with hDPSCs/OF. Furthermore, the PLGC scaffold gradually degraded, as evidenced by the fluorescent-labeled PLGC scaffold, which provides information to tract biodegradation of implanted PLGC scaffold. In conclusion, we confirmed neo-bone formation within a cranial bone defect using hDPSCs and a computer-designed PLGC scaffold.

Original languageEnglish
Article number12721
JournalScientific Reports
Volume5
DOIs
StatePublished - 2015.08.3

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