The role of APCDD1 in epithelial rearrangement in tooth morphogenesis

被引:0
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作者
Sanjiv Neupane
Wern-Joo Sohn
Gi-Jeong Gwon
Ki-Rim Kim
Sanggyu Lee
Chang-Hyeon An
Jo-Young Suh
Hong-In Shin
Hitoshi Yamamoto
Sung-Won Cho
Youngkyun Lee
Jae-Young Kim
机构
[1] Kyungpook National University,Department of Biochemistry, School of Dentistry, IHBR
[2] Kyungpook National University,Department of Dental Hygiene, IHBR
[3] Kyungpook National University,School of Life Science and Biotechnology
[4] Kyungpook National University,Department of Oral and Maxillofacial Radiology, School of Dentistry, IHBR
[5] Kyungpook National University,Department of Periodontology, School of Dentistry, IHBR
[6] Kyungpook National University,Department of Oral and Maxillofacial Pathology, School of Dentistry, IHBR
[7] Tokyo Dental College,Department of Histology and Developmental Biology
[8] Yonsei University College of Dentistry,Division in Anatomy and Developmental Biology, Department of Oral Biology
来源
Histochemistry and Cell Biology | 2015年 / 144卷
关键词
APCDD1; Epithelial rearrangement; Inner enamel epithelium; Enamel knot; Cusp patterning;
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摘要
Adenomatosis polyposis coli downregulated 1 (APCDD1), a negative regulator of Wnt signaling, was examined to understand detailed mechanisms underlying Wnt signaling tooth development. In situ hybridization showed that Apcdd1 was expressed in the condensed mesenchyme at the bud stage, and in the inner enamel epithelium (IEE), including enamel knot (EK) at the cap stage. In vitro organ cultivation by using Apcdd1 antisense oligodeoxynucleotides was performed at E13.5 for 2 days to define the developmental functions of APCDD1 during tooth development. Analysis of histogenesis and cellular events such as cell adhesion, proliferation, apoptosis and epithelial rearrangement after Apcdd1 knockdown showed altered morphogenesis of the tooth germ with decreased cell proliferation and altered localization of cell adhesion molecules. Actin filament staining and 1,1′-dioctadecyl-3,3,3′,3′-tetramethylindocarbocyanine perchlorate (DiI) labeling of IEE cells showed that Apcdd1 knockdown enhanced epithelial rearrangement in the IEE and EK. To understand the precise signaling regulations of Apcdd1, we evaluated the altered expression patterns of signaling molecules, related with Wnt and enamel knot signalings using RT-qPCR. Tooth germs at cap stage were transplanted into the kidney capsules and were allowed to develop into calcified teeth for 3 weeks. Apcdd1 knockdown increased the number of ectopic cusps on the mesial side of the tooth. Our results suggested that APCDD1 modulates the gene expression of Wnt- and EK-related signaling molecules at the cap stage of tooth development, and is involved in tooth cusp patterning by modulating the epithelial rearrangement in the IEE.
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页码:377 / 387
页数:10
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