Primary and secondary culture of rat ameloblasts in serum-free medium

Akiko Kukita, Hidemitsu Harada, Toshio Kukita, Tetsuichiro Inai, Sachiko Matsuhashi, Kojiro Kurisu

Research output: Contribution to journalArticlepeer-review

29 Citations (Scopus)

Abstract

Enamel is the hardest tissue in vertebrates. Ameloblasts are derived from epithelial cells and are responsible for enamel formation. They secrecte enamel matrix components in which amelogenins are the major proteins, the biochemical properties of which are well known. However, little is known about the characteristics of ameloblasts themselves or about the functions of amelogenins. In this study, we developed a novel primary and secondary culture system for ameloblasts using a monoclonal antibody which recognized amelogenin (En3). The cell layer on dentine removed from rat mandibular incisors was isolated and cultured in low calcium, serum-free medium. Primary culture was performed on collagen-coated culture plates and typically, two types of cells appeared. One major type changed morphology after the addition of a high concentration of calcium to the medium. Expression of amelogenin was shown as cytoplasmic particles in these cells using En3. In the secondary culture, expression of amelogenins was also observed. In this system, the cells grew and maintained the expression of amelogenin for about 3 weeks.

Original languageEnglish
Pages (from-to)393-398
Number of pages6
JournalCalcified Tissue International
Volume51
Issue number5
DOIs
Publication statusPublished - Nov 1 1992

All Science Journal Classification (ASJC) codes

  • Endocrinology, Diabetes and Metabolism
  • Orthopedics and Sports Medicine
  • Endocrinology

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