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Published on: November 1, 2021
Receptor related to tyrosine kinase RYK regulates cell migration during cortical development
Kazuyo Kamitori1, Mayumi Tanaka, Takae Okuno-Hirasawa
1Department of Neurochemistry, National Institute of Neuroscience, 4-1-1 Ogawa-higashi, Kodaira, Tokyo 187-8502, Japan.
Abstract:
Mammalian RYK is a receptor related to tyrosine kinase without detectable catalytic activity. We have previously reported that rat RYK is dominantly expressed in neural progenitor cells and mature neurons in the developing central nervous system. Mouse RYK has been found to bind to EphB2/B3 receptors, which have diverse functions during development. In this study, we demonstrated that RYK, EphB2, EphB3, ephrinB1, and ephrinB2 are expressed in embryonic brain. In vitro analysis using COS-7 cells revealed binding between rat RYK and EphB3, and that the RYK deletion mutant without extracellular leucine-rich motifs lacked this binding ability. To investigate the function of RYK in vivo, embryonic cortical slice cultures were analyzed after electroporation of expression plasmids for RYK or its deletion mutants. The results showed that overexpression of RYK suppressed cell migration from the ventricular zone to the pial surface, however, overexpression of the RYK deletion mutant without leucine-rich motifs had no effect on cell migration. These results suggest that RYK regulates cell migration during mammalian cortical development through the binding to Eph receptors.
Insights
Receptor tyrosine kinase (RYK) in mammals regulates neural progenitor cell migration during embryonic brain development. This regulation occurs through RYK
Area of Science:
- Neuroscience
- Developmental Biology
- Molecular Biology
Background:
- Mammalian RYK, a receptor tyrosine kinase, is predominantly expressed in the developing central nervous system.
- RYK lacks detectable catalytic activity but interacts with EphB receptors, crucial for developmental processes.
Purpose of the Study:
- To investigate the role of RYK in mammalian cortical development.
- To elucidate the mechanism by which RYK influences neural cell migration.
Main Methods:
- Expression analysis of RYK, EphB2, EphB3, ephrinB1, and ephrinB2 in embryonic brains.
- In vitro binding assays using COS-7 cells to assess RYK-EphB3 interactions.
- In vivo functional analysis using embryonic cortical slice cultures with RYK overexpression.
Main Results:
- RYK, EphB2, EphB3, ephrinB1, and ephrinB2 are co-expressed in the embryonic brain.
- Rat RYK binds to EphB3, dependent on its extracellular leucine-rich motifs.
- RYK overexpression suppresses neural progenitor cell migration in cortical slice cultures.
Conclusions:
- RYK plays a critical role in regulating mammalian cortical development.
- RYK mediates neural progenitor cell migration via binding to Eph receptors.
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