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Journal of Histochemistry and Cytochemistry
Volume 51 (12): 1673-1679, 2003
Copyright ©The Histochemical Society, Inc.

Fibronectin Accelerates the Growth and Differentiation of Ameloblast Lineage Cells In Vitro

Makoto J. Tabata, Tatsushi Matsumura, Takafumi Fujii, Makoto Abe and Kojiro Kurisu

Anatomy for Oral Science, Department of Neurology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan (MJT); Department of Oral Anatomy and Developmental Biology, Osaka University Faculty of Dentistry, Osaka, Japan (TM,TF,MA); and Yukioka School of Allied Health Professions, Osaka, Japan (KK)

Correspondence to: Makoto J. Tabata, Anatomy for Oral Science, Department of Neurology, Kagoshima University Graduate School of Medical and Dental Sciences, 8-35-1, Sakuragaoka, Kagoshima 890-8544, Japan. E-mail: mtabata{at}denta.hal.kagoshima-u.ac.jp

During tooth development, the growth and differentiation of ameloblast lineage (AL) cells are regulated by epithelial–mesenchymal interactions. To examine the dynamic effects of components of the basement membrane, which is the extracellular matrix (ECM) lying between the epithelium and mesenchyme, we prepared AL cells from the epithelial layer sheet of mandibular incisors of postnatal day 7 rats and cultured them on plates coated with type IV collagen, laminin-1, or fibronectin. The growth of AL cells was supported by type IV collagen and fibronectin but not by laminin-1 in comparison with that on type I collagen as a reference. Clustering and differentiation of AL cells were observed on all matrices examined. AL cells showed normal growth and differentiation at low cell density on fibronectin but not on type I collagen. Furthermore, the population of cytokeratin 14-positive cells on fibronectin was lower than that on other ECM components, suggesting that fibronectin may be a modulator to accelerate the differentiation of AL cells. After the cells had been cultured for 9 days on fibronectin, crystal-like structures were observed. These structures overlaid the cell clusters and were positive for von Kossa staining. These findings indicate that each matrix component has a regulative role in the proliferation and differentiation of AL cells and that fibronectin causes the greatest acceleration of AL cell differentiation. (J Histochem Cytochem 51:1673–1679, 2003)

Key Words: fibronectin • laminin-1 • type IV collagen • type I collagen • ameloblast lineage cells • crystal-like structures


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