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Published on: September 24, 2014
Expression of delta-protocadherins in the spinal cord of the chicken embryo
Juntang Lin1, Congrui Wang, Christoph Redies
1Institute of Anatomy I, University of Jena School of Medicine, Jena University Hospital, D-07743 Jena, Germany.
Insights
This study maps the expression of eight delta-protocadherins in the developing chicken spinal cord. These cadherin genes show specific spatial and temporal patterns, suggesting diverse roles in neural development.
Area of Science:
- Developmental Biology
- Neuroscience
- Genetics
Background:
- Protocadherins are the largest cadherin gene subfamily, crucial for nervous system development.
- Understanding their specific roles requires detailed expression analysis.
Purpose of the Study:
- To clone and investigate the expression patterns of eight delta-protocadherin genes in the developing chicken spinal cord.
- To elucidate the spatiotemporal distribution of these genes during embryonic development.
Main Methods:
- Cloning of eight delta-protocadherin genes (Pcdh1, Pcdh7, Pcdh8, Pcdh9, Pcdh10, Pcdh17, Pcdh18, Pcdh19) from chicken.
- In situ hybridization to analyze gene expression in the developing spinal cord at various embryonic stages (E2.5–E10).
Main Results:
- All eight delta-protocadherins displayed spatially restricted and temporally regulated expression patterns.
- Distinct expression domains were observed in the neuroepithelial layer, mantle layer, motor column, and dorsal root ganglion.
- Specific cadherins were localized to surrounding tissues including meninges, notochord, dermomyotome, and sclerotome.
Conclusions:
- The diverse and highly regulated spatiotemporal expression of delta-protocadherins indicates multifaceted functions in spinal cord and associated tissue development.
- These findings provide a foundation for further research into the specific roles of individual delta-protocadherins in neural patterning and cell differentiation.
Abstract:
Protocadherins constitute the largest subfamily of cadherin genes and are widely expressed in the nervous system. In the present study, we cloned eight members of the delta-protocadherin subfamily of cadherins (Pcdh1, Pcdh7, Pcdh8, Pcdh9, Pcdh10, Pcdh17, Pcdh18, and Pcdh19) from the chicken, and investigated their expression in the developing chicken spinal cord by in situ hybridization. Our results showed that each of the investigated delta-protocadherins exhibits a spatially restricted and temporally regulated pattern of expression. Pcdh1, Pcdh8, Pcdh18, and Pcdh19 are expressed in restricted dorsoventral domains of the neuroepithelial layer at early developmental stages (E2.5–E4). In the differentiating mantle layer, specific expression profiles are observed for all eight delta-protocadherins along the dorsoventral, mediolateral, and rostrocaudal dimensions at intermediate stages of development (E6–E10). Expression profiles are especially diverse in the motor column, where different pools of motor neurons exhibit signal for subsets of delta-protocadherins. In the dorsal root ganglion, subpopulations of cells express combinations of Pcdh1, Pcdh7, Pcdh8, Pcdh9, Pcdh10, and Pcdh17. The ventral boundary cap cells are positive for Pcdh7, Pcdh9, and Pcdh10. Signals for Pcdh8, Pcdh18, and Pcdh19 are found in the meninges. Surrounding tissues, such as the notochord, dermomyotome, and sclerotome also exhibit differential expression patterns. The highly regulated spatiotemporal expression patterns of delta-protocadherins suggest that they have multiple and diverse functions during development of the spinal cord and its surrounding tissues.
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