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FGF-9 accelerates epithelial invagination for ectodermal organogenesis in real time bioengineered organ manipulation
Yun-Yuan Tai1, Rung-Shu Chen, Yi Lin
1Graduate Institute of Clinical Dentistry, School of Dentistry, National Taiwan University, Taipei, 10002, Taiwan. tyling@ntu.edu.tw.
Cell Communication and Signaling : CCS
|November 27, 2012
Summary
Fibroblast growth factor-9 (FGF-9) accelerates epithelial invagination and ectodermal organogenesis in a real-time study. This finding suggests FGF-9
Area of Science:
- Developmental Biology
- Regenerative Medicine
- Bioengineering
Background:
- Epithelial invagination is crucial for ectodermal organogenesis.
- Real-time studies on factors influencing ectodermal organogenesis are limited.
- Electric cell-substrate impedance sensing (ECIS) offers real-time monitoring of cell layer changes.
Purpose of the Study:
- To establish a bioengineered organ-ECIS model for real-time analysis.
- To investigate the effects of fibroblast growth factor-9 (FGF-9) on epithelial invagination.
- To explore FGF-9's role in epithelial-mesenchymal interactions during ectodermal organ development.
Main Methods:
- Dissection of epithelial and mesenchymal cells from murine molar tooth germs (E14.5).
- Establishment of a combined bioengineered organ-Electric cell-substrate impedance sensing (ECIS) model.
- Real-time monitoring of bioengineered ectodermal organ thickness and gene expression.
Main Results:
- Fibroblast growth factor-9 (FGF-9) was shown to accelerate epithelial invagination within 3 days.
- FGF-9 stimulates and sustains the expression of Ameloblastin and Amelogenin during odontogenesis.
- The study provides the first real-time data on FGF-9's role in epithelial invagination.
Conclusions:
- FGF-9 plays a significant role in initiating epithelial invagination and ectodermal organogenesis.
- FGF-9 holds potential for ectodermal organ regeneration research.
- The bioengineered organ-ECIS model is a promising tool for ectodermal organ engineering.

