In vitro growth and differentiated activities of human periodontal ligament fibroblasts cultured on salmon collagen gel
Article first published online: 12 FEB 2007
DOI: 10.1002/jbm.a.31110
Copyright © 2007 Wiley Periodicals, Inc.
Issue
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Journal of Biomedical Materials Research Part A
Volume 82A, Issue 2, pages 395–402, August 2007
Additional Information
How to Cite
Nagai, N., Mori, K., Satoh, Y., Takahashi, N., Yunoki, S., Tajima, K. and Munekata, M. (2007), In vitro growth and differentiated activities of human periodontal ligament fibroblasts cultured on salmon collagen gel. J. Biomed. Mater. Res., 82A: 395–402. doi: 10.1002/jbm.a.31110
Publication History
- Issue published online: 14 JUN 2007
- Article first published online: 12 FEB 2007
- Manuscript Accepted: 18 SEP 2006
- Manuscript Revised: 18 AUG 2006
- Manuscript Received: 19 JUL 2006
- Abstract
- Article
- References
- Cited By
Keywords:
- salmon collagen;
- periodontal ligament fibroblasts;
- growth rate;
- alkaline phophatase activity;
- quantitative RT-PCR
Abstract
Marine-derived collagen is expected to be a much safer alternative to calf collagen, which in medical applications carries the risk of bovine spongiform encephalopathy. In this study, acid-soluble collagen was extracted from salmon skin and crosslinked with 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide during fibril formation to produce a crosslinked salmon collagen (SC) gel. The growth rates and the differentiated functions of human periodontal ligament fibroblasts (HPdLFs) cultured on the SC gel were investigated. Growth was faster on the SC gel than on porcine collagen (PC) gel. In addition, the HPdLFs cultured on the SC gel exhibited higher alkaline phosphatase (ALP) activity than those cultured on the PC gel. Quantitative RT-PCR revealed higher mRNA expression of type I collagen, ALP, and osteocalcin in the HPdLFs cultured on the SC gel. HPdLFs had a flat shape on the SC gel and a spindle shape on the PC gel, as revealed by observation with scanning electron microscopy and immunostaining with cytoskeletal protein and vinculin. The results showed that HPdLFs could grow and show highly differentiated activity on the SC gel as well as on the PC gel. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res, 2007

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