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Deciphering Axonal Pathways of Genetically Defined Groups of Neurons in the Chick Neural Tube Utilizing in ovo Electroporation
Published on: May 2, 2010
Distribution of OL-protocadherin in axon fibers in the developing chick nervous system
Shinsuke Nakao1, Masato Uemura, Eiko Aoki
1RIKEN Center for Developmental Biology, 2-2-3 Minatojima-Minamimachi, Chuou-ku Kobe 650-0047, Japan.
Insights
OL-protocadherin (OL-pc) is crucial for neural development. This study reveals OL-pc
Area of Science:
- Neuroscience
- Developmental Biology
- Molecular Biology
Background:
- OL-protocadherin (OL-pc) is a homophilic cell adhesion molecule within the cadherin superfamily.
- Understanding OL-pc's role is vital for comprehending neural development and axon guidance.
Purpose of the Study:
- To clone and characterize the chicken homologue of OL-protocadherin (OL-pc).
- To investigate the expression pattern of OL-pc in early chick embryos (E3.5-E6.5).
- To elucidate the potential functions of OL-pc in neural development, particularly axon navigation.
Main Methods:
- Cloning and characterization of chicken OL-pc.
- Expression pattern analysis using immunohistochemistry in chick embryos.
- Comparative analysis of chick and mammalian OL-pc structures.
Main Results:
- Chick OL-pc structure is similar to mammalian counterparts.
- OL-pc protein is prominently expressed in developing axonal fibers in the brain and peripheral nervous system.
- Specific expression in motor neurons and motor nerves, with distinct segregation patterns observed in nerve plexuses and along branchial nerves.
Conclusions:
- OL-pc plays a significant role in early neural development.
- Evidence suggests OL-pc involvement in axon elongation, selective fasciculation, and pathfinding.
- OL-pc may guide motor axons and contribute to their segregation from sensory axons.
Abstract:
OL-protocadherin (OL-pc) is a homophilic cell adhesion molecule that belongs to the cadherin gene superfamily. We cloned and characterized the chicken homologue of OL-pc and examined its expression pattern in chick embryos mainly from embryonic day (E) 3.5 to E6.5. The structure of chick OL-pc was found to be essentially the same as that of mammalian OL-pc's except for some small deletions and insertions in the amino acid sequence. OL-pc protein was detected prominently along developing axonal fibers in the brain and also in the peripheral nervous system. In addition, it was detected in some mesenchymal cells and in the embryonic ectoderm of the mandible and limb bud. In the spinal cord, OL-pc was specifically expressed in motor neurons, and the protein was distributed along motor nerves. Motor nerves merged gradually with sensory nerves showing negative/faint OL-pc expression, but their fibers remained separated as small bundles in the nerves. Interestingly, OL-pc-positive motor nerves such as those to the sternocoracoideus became segregated from OL-pc-faint/weak motor nerves at the plexus region. Moreover, OL-pc was distributed along the path of the branchial nerves. These results suggest that OL-pc might play some roles in axon navigation such as in axon elongation, selective fasciculation, and pathfinding in the early stage of neural development.
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