J Korean Assoc Oral Maxillofac Surg.  2001 Oct;27(5):453-456.

Isolation Of Human Alveolar Bone-Derived Cells And In Vitro Amplification For Tissue Engineering

Affiliations
  • 1Department of Oral and Maxillofacial Surgery, College of Dentistry, Yonsei University, Korea. E-mail:choibh@wonju.yonsei.ac.kr
  • 2Department of Dentistry, Asan Kangnung Hospital, Kangnung, Korea.

Abstract

BACKGROUND: Autogenous alveolar bone cell transplantation may be suitable for tissue engineering for alveolar bone reconstruction. This study aimed to isolate human alveolar bone-derived cells (HABDCs) and to evaluate the ability of collagen gels to support HABDC proliferation and differentiation for human alveolar bone tissue engineering applications. METHOD: Cultures of primary HABDCs were established from alveolar bone chips obtained from 10 persons undergoing tooth extraction. These cells were expanded in vitro until passage 3 and used for the in vitro characterization of HABDCs and the in vitro analysis of collagen gels for alveolar bone tissue engineering.
RESULTS
Of the 10 attempts made to obtain HABDC cultures, eight were successful. HABDCs expressed the osteoblastic phenotype characterized by alkaline phosphatase activity, osteocalcin expression and the mineralization of the extracellular matrix in vitro. When seeded on collagen gels, HABDCs penetrated into the collagen gel matrices and proliferated inside the gels. Significantly, when HABDCs were embedded into the gels, collagen fibers and mineralization were produced within the gels.
CONCLUSION
This study demonstrates the feasibility of using cultured HABDCs and collagen gels for human alveolar bone tissue engineering applications.

Keyword

Alveolar bone; Tissue engineering; Bone regeneration

MeSH Terms

Alkaline Phosphatase
Bone and Bones
Bone Regeneration
Cell Transplantation
Collagen
Extracellular Matrix
Gels
Humans*
Osteoblasts
Osteocalcin
Phenotype
Tissue Engineering*
Tooth Extraction
Transplants
Alkaline Phosphatase
Collagen
Gels
Osteocalcin
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