The Role of the Wnt Signaling Pathway in Upper Jaw Development of Chick Embryo
Autor: | Masayoshi Kawakami, Akio Wanaka, Tadaaki Kirita, Kouko Tatsumi, Shoko Morita-Takemura, Tatsuhide Tanaka, Tadahiro Shimomura |
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Rok vydání: | 2019 |
Předmět: |
TBX22
animal structures Histology Physiology Morphogenesis SOX9 cleft lip Biology Biochemistry Pathology and Forensic Medicine Dickkopf-1 03 medical and health sciences chick embryo N-cadherin 030304 developmental biology 0303 health sciences 030302 biochemistry & molecular biology Wnt signaling pathway Regular Article Embryo Cell Biology Wnt signaling Cell biology Maxillary prominence embryonic structures Signal transduction WNT3A |
Zdroj: | Acta Histochemica et Cytochemica |
ISSN: | 1347-5800 0044-5991 |
DOI: | 10.1267/ahc.18038 |
Popis: | Cleft lip with or without cleft palate (CLP) usually results from a failure of the medial nasal prominences to fuse with the lateral and maxillary prominences. This failure inhibits facial morphogenesis regulated by several major morphogenetic signaling pathways. We hypothesized that CLP results from the failure of the Wnt signaling pathway. To examine whether Wnt signaling can influences upper jaw development, we applied beads soaked with Dickkopf-1 (Dkk-1), Alsterpaullone (AL) or Wnt3a to the right side of the maxillary prominence of the chick embryo. The embryo showed a defect of the maxilla on the treated side, and skeletal staining revealed hypoplasia of the premaxilla and palatine bone as a result of Dkk-1-soaked bead implantation. 5-bromo-2'-deoxyuridine (BrdU)-positive cell numbers in the treated maxillary prominence were significantly lower at both 24 and 48 hr after implantation. Down-regulation of the expression of Bmp4, Tbx22, Sox9, and Barx1 was confirmed in the maxillary prominence treated with Dkk-1, which indicated that the deformity of the maxillary bone was controlled by gene targets of the Wnt signaling pathway. Expression of N-cadherin was seen immunohistochemically in the maxillary prominences of embryos at 6 hr and increased at 24 hr after AL treatment. Wnt signaling enhanced by AL or Wnt3a up-regulated the expression levels of Msx1, Bmp4, Tbx22, Sox9, and Barx1. Our data suggest that the Wnt signaling pathway regulates maxillary morphogenesis and growth through Bmp4, Tbx22, Sox9, and Barx1. Wnt signaling might regulate N-cadherin expression via Msx1, resulting in cell aggregation for osteochondrogenesis. |
Databáze: | OpenAIRE |
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