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Grafting of Beads into Developing Chicken Embryo Limbs to Identify Signal Transduction Pathways Affecting Gene Expression
Published on: January 17, 2016
Inhibition of Wnt/β-catenin pathway by Dickkopf-1 [corrected] affects midfacial morphogenesis in chick embryo
Masayoshi Kawakami1, Hiroaki Okuda2, Kouko Tatsumi2
1Department of Oral and Maxillofacial Surgery, Nara Medical University, 840 Shijo-cho, Kashihara, Nara 634-8522, Japan.
Abstract:
The development of the vertebrate face is regulated by complex interactions among several signaling pathways. Dickkopf-1 (Dkk-1), an inhibitor of the Wnt/β-catenin signaling pathway, can affect midfacial morphogenesis. The downstream target genes of the Wnt/β-catenin signaling pathway in morphogenesis of the developing upper jaw and lip remain unknown. To investigate the functional roles of Wnt/β-catenin signaling in facial development, we performed a loss-of-function experiment using local implantation of beads soaked with Dkk-1 during lip fusion at the maxillary prominence of chick embryos at stage 22(HH22). Antagonism of Wnt/β-catenin signaling by Dkk-1 induced deformities of the premaxilla and jugal bone, which are derived from the maxillary mesenchyme. Real-time and semi-quantitative RT-PCR analysis showed the significant reduction of Lhx8, Msx1 and Msx2 expression levels around the beads in the maxillary mesenchyme at 6 and 24 h after bead implantation. Time course experiments in the HH 22 embryos showed the effect of Dkk-1 on Lhx8, Msx1 and Msx2 expression was not significant after 48 h of the treatment. At HH 26 when the fusion of facial primordial started, Dkk-1 application did not exhibit any significant reduction of those genes. Our findings suggested that Dkk-1 regulates maxillary morphogenesis in chick embryos through Lhx8, Msx1 and Msx2 signals. Wnt/β-catenin signaling is responsible for intrinsic upper jaw development before the lip fusion.
Insights
Dickkopf-1 (Dkk-1) inhibits Wnt/β-catenin signaling, impacting chick embryo midfacial development. Dkk-1 disrupts upper jaw and lip formation by reducing Lhx8, Msx1, and Msx2 gene expression during critical developmental stages.
Area of Science:
- Developmental Biology
- Molecular Biology
- Genetics
Background:
- Vertebrate facial development involves intricate signaling pathways.
- Dickkopf-1 (Dkk-1), a Wnt/β-catenin pathway inhibitor, influences midfacial morphogenesis.
- Downstream targets of Wnt/β-catenin in upper jaw and lip development are not fully understood.
Purpose of the Study:
- Investigate the role of Wnt/β-catenin signaling in facial development.
- Determine the impact of Dkk-1 on maxillary prominence development.
- Identify downstream genes regulated by Wnt/β-catenin signaling during facial fusion.
Main Methods:
- Loss-of-function experiment using Dkk-1 soaked beads in chick embryos (HH22).
- Local implantation at the maxillary prominence during lip fusion.
- Real-time and semi-quantitative RT-PCR to analyze gene expression (Lhx8, Msx1, Msx2).
Main Results:
- Dkk-1 implantation caused premaxilla and jugal bone deformities.
- Significant reduction in Lhx8, Msx1, and Msx2 expression observed at 6 and 24 hours post-implantation.
- No significant effect on gene expression after 48 hours or at later developmental stages (HH26).
Conclusions:
- Dkk-1 regulates maxillary morphogenesis in chick embryos via Lhx8, Msx1, and Msx2.
- Wnt/β-catenin signaling is crucial for intrinsic upper jaw development prior to lip fusion.
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