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The Slice Culture Method for Following Development of Tooth Germs In Explant Culture
Published on: November 13, 2013
Possible functional involvement of thymosin beta 4 in developing tooth germ of mouse lower first molar
Merina Akhter1, Ieyoshi Kobayashi, Tamotsu Kiyoshima
1Laboratory of Oral Pathology and Medicine, Kyushu University Graduate School of Dental Science, 3-1-1 Maidashi, Fukuoka, 812-8582, Japan.
Abstract:
We examined the detailed in situ expression pattern of thymosin beta 4 (Tbeta4) in the developing mouse mandibular first molar. Tbeta4 mRNA was expressed in the presumptive dental epithelium at embryonic day 10.5 (E10.5) and in the thickened dental epithelium at E12. An in situ signal was observed in the invaginated epithelial bud at E13, in the enamel organ at E14 and E14.5, and in the primary enamel knot (PEK) at E14.5. The signal was localized in the epithelial cells of the outer layer of the enamel organ at E15 and E15.5. No signal was found in the PEK at these stages. Tbeta4 mRNA was expressed in the inner enamel epithelium, cervical loop and dental lamina at E16 and E17. The expression of Tbeta4 mRNA was observed in the polarized inner epithelial cells at E18, newborn day 1 (N1) and N2. However, the signal intensity decreased markedly at N3. We herein report for the first time that Tbeta4 is distinctly expressed in developing tooth germ, and it may also play functional roles in the initiation, growth and differentiation of tooth germ.

