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New Insights Into Cranial Synchondrosis Development: A Mini Review
1Department of Signal Gene Regulation, Tokyo Medical and Dental University, Tokyo, Japan.
Frontiers in Cell and Developmental Biology
|August 28, 2020
Summary
Cranial base synchondroses are key growth centers. Signaling pathways and transcription factors regulate their development, with gene disruptions causing varied skeletal abnormalities.
Area of Science:
- Developmental Biology
- Craniofacial Development
- Molecular Biology
Background:
- Synchondroses, crucial growth centers in the cranial base, are formed via endochondral ossification and influence neurocranium and craniofacial bone development.
- Two central cranial base synchondroses, the intersphenoid and spheno-occipital synchondroses, function as mirror-image bipolar growth plates.
- Abnormalities in these synchondroses lead to impaired cranial base elongation and affect adjacent craniofacial structures.
Purpose of the Study:
- To review the developmental processes of cranial synchondroses.
- To elucidate the regulatory roles of signaling pathways and transcription factors in synchondrosis development.
- To highlight the distinct developmental differences between the intersphenoid and spheno-occipital synchondroses.
Main Methods:
- Review of existing literature on cranial synchondrosis development.
- Analysis of the roles of key signaling pathways: parathyroid hormone-like hormone (PTHLH)/parathyroid hormone-related protein (PTHrP), Indian hedgehog (Ihh), Wnt/β-catenin, and fibroblast growth factor (FGF).
- Examination of the involvement of transcription factors (RUNX2, SIX1, SIX2, SIX4, TBX1) and cilium assembly in synchondrosis development.
Main Results:
- Signaling pathways and transcription factors are critical regulators of synchondrosis development.
- Gene disruptions in mice result in abnormal ossification of cranial synchondroses and skeletal elements.
- Distinct and overlapping abnormalities are observed in the intersphenoid and spheno-occipital synchondroses following gene disruption.
Conclusions:
- Cranial synchondrosis development is a complex process regulated by intricate molecular signaling networks.
- Understanding these pathways and transcription factors is essential for comprehending craniofacial development and associated abnormalities.
- The intersphenoid and spheno-occipital synchondroses exhibit unique developmental characteristics and responses to genetic perturbations.
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