PMID- 16707102 OWN - NLM STAT- MEDLINE DCOM- 20060801 LR - 20220318 IS - 0006-291X (Print) IS - 0006-291X (Linking) VI - 345 IP - 3 DP - 2006 Jul 7 TI - Establishment of primary cultures for mouse ameloblasts as a model of their lifetime. PG - 1247-53 AB - To understand how the properties of ameloblasts are spatiotemporally regulated during amelogenesis, two primary cultures of ameloblasts in different stages of differentiation were established from mouse enamel epithelium. Mouse primary ameloblasts (MPAs) prepared from immature enamel epithelium (MPA-I) could proliferate, whereas those from mature enamel epithelium (MPA-M) could not. MPA-M but not MPA-I caused apoptosis during culture. The mRNA expression of amelogenin, a marker of immature ameloblasts, was down-regulated, and that of enamel matrix serine proteiase-1, a marker of mature ameloblasts, was induced in MPA-I during culture. Using green fluorescence protein as a reporter, a visualized reporter system was established to analyze the promoter activity of the amelogenin gene. The region between -1102bp and -261bp was required for the reporter expression in MPA-I. These results suggest that MPAs are valuable in vitro models for investigation of ameloblast biology, and that the visualized system is useful for promoter analysis in MPAs. FAU - Suzawa, Tetsuo AU - Suzawa T AD - Department of Biochemistry, School of Dentistry, Showa University, Tokyo 142-8555, Japan. suzawa@dent.showa-u.ac.jp FAU - Itoh, Nao AU - Itoh N FAU - Takahashi, Naoyuki AU - Takahashi N FAU - Katagiri, Takenobu AU - Katagiri T FAU - Morimura, Naoko AU - Morimura N FAU - Kobayashi, Yasuna AU - Kobayashi Y FAU - Yamamoto, Toshinori AU - Yamamoto T FAU - Kamijo, Ryutaro AU - Kamijo R LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20060502 PL - United States TA - Biochem Biophys Res Commun JT - Biochemical and biophysical research communications JID - 0372516 RN - G34N38R2N1 (Bromodeoxyuridine) SB - IM MH - Ameloblasts/*cytology MH - Animals MH - Apoptosis MH - Bromodeoxyuridine/pharmacology MH - Cell Culture Techniques/*methods MH - Cell Differentiation MH - Cell Proliferation MH - Cells, Cultured MH - Dental Enamel/*cytology MH - Gene Deletion MH - Genes, Reporter MH - In Situ Nick-End Labeling MH - Mice MH - Promoter Regions, Genetic EDAT- 2006/05/19 09:00 MHDA- 2006/08/02 09:00 CRDT- 2006/05/19 09:00 PHST- 2006/03/29 00:00 [received] PHST- 2006/04/17 00:00 [accepted] PHST- 2006/05/19 09:00 [pubmed] PHST- 2006/08/02 09:00 [medline] PHST- 2006/05/19 09:00 [entrez] AID - S0006-291X(06)00932-6 [pii] AID - 10.1016/j.bbrc.2006.04.122 [doi] PST - ppublish SO - Biochem Biophys Res Commun. 2006 Jul 7;345(3):1247-53. doi: 10.1016/j.bbrc.2006.04.122. Epub 2006 May 2.