Medical Journals

In Vitro Growth and Differentiated Activities of Human Periodontal Ligament Fibroblasts Cultured on Salmon Collagen Gel.

Authors:
  • Nagai Nobuhiro
  • Mori Kazuo
  • Satoh Yasuharu
  • Takahashi Noritaka
  • Yunoki Shunji
  • Tajima Kenji
  • Munekata Masanobu

From: Creative Research Initiative “Sousei” (CRIS), Hokkaido University, N21-W10, Kita-ku, Sapporo, Hokkaido 001-0021, Japan. nagai@cris.hokudai.ac.jp

Journal of biomedical materials research. Part A

  • Publish Date: Aug 2007
  • ISSN: 1549-3296
  • Volume: 82
  • Issue: 2
  • Pages: 395-402
  • Medium: Print
  • Language: English
  • Citation (JAMA): Nagai Nobuhiro, Mori Kazuo, Satoh Yasuharu, et al. In Vitro Growth and Differentiated Activities of Human Periodontal Ligament Fibroblasts Cultured on Salmon Collagen Gel.. Aug 2007;82:395-402

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.

Mesh Headings (Keywords): Alkaline Phosphatase, Animals, Base Sequence, Biocompatible Materials, Cell Differentiation, Cell Proliferation, Cell Shape, Cells, Cultured, Collagen, Collagen Type I, DNA Primers, Fibroblasts, Gels, Humans, Materials Testing, Microscopy, Electron, Scanning, Osteocalcin, Periodontal Ligament, RNA, Messenger, Salmon, Swine


Check for Full Text / PubMed Unique Identifier (PMID): 17295232


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


Advertisements

About | Privacy Policy | Business Solutions | Advertise | Contact | Add Healia to your site

©2012. Healia / Meredith Corporation  

Use of this site constitutes acceptance of our Terms of Service and Privacy Policy. All content on this Web site, including medical opinion and any other health-related information, is for informational purposes only and should not be used for a specific diagnosis or individual treatment plan for any situation. Use of this site and the information contained herein does not create a doctor-patient relationship. Always seek the direct advice of your doctor in connection with any questions or issues you may have regarding your own health or the health of others.