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Sox11 Balances Dendritic Morphogenesis with Neuronal Migration in the Developing Cerebral Cortex
Yoshio Hoshiba1, Tomohisa Toda1, Haruka Ebisu1
1Department of Medical Neuroscience, Graduate School of Medical Sciences, and Brain/Liver Interface Medicine Research Center, Kanazawa University, Ishikawa 920-8640, Japan, Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, Japan, and.
The transcription factor Sox11 suppresses dendritic morphogenesis in the developing cerebral cortex. Its reduction is essential for proper neuronal migration and the formation of the cerebral cortex.
Area of Science:
- Neuroscience
- Developmental Biology
- Molecular Biology
Background:
- Coordinated regulation of dendritic morphogenesis is vital for cerebral cortex development.
- While factors promoting dendritic growth are known, those suppressing it remain largely unidentified.
Purpose of the Study:
- To investigate the role of transcription factors in suppressing dendritic morphogenesis during cerebral cortex development.
- To identify novel molecular mechanisms governing neuronal structure formation.
Main Methods:
- Utilized loss- and gain-of-function studies.
- Employed postnatal and in utero electroporation techniques in mouse models.
- Analyzed Sox11 expression levels during dendritic morphogenesis.
Main Results:
- Sox11 expression significantly decreases during dendritic morphogenesis.
- Sox11 acts as a necessary and sufficient inhibitor of dendritic morphogenesis in excitatory cortical neurons.
- Early Sox11 suppression led to premature neurite branching and neuronal migration defects.
- Radial migration completion correlated with reduced Sox11 expression.
Conclusions:
- Sox11-mediated suppression of dendritic morphogenesis during radial migration is critical for cerebral cortex formation.
- Sox11 plays a key role in balancing neuronal development and migration.
- These findings reveal a novel mechanism regulating neuronal structure and cortical development.
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