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Multi-Photon Time Lapse Imaging to Visualize Development in Real-time: Visualization of Migrating Neural Crest Cells in Zebrafish Embryos
Published on: August 9, 2017
Zebrafish foxd3 is selectively required for neural crest specification, migration and survival
Rodney A Stewart1, Brigitte L Arduini, Stephane Berghmans
1Department of Pediatric Oncology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA.
The foxd3 gene is crucial for neural crest cell development in zebrafish. It regulates cell fate specification, migration, and survival, impacting neuronal, glial, and cartilage cell formation.
Area of Science:
- Developmental Biology
- Genetics
- Neuroscience
Background:
- The vertebrate neural crest is a multipotent stem cell population.
- Neural crest cell fate determination mechanisms are not fully understood.
- The foxd3 gene encodes a transcription factor vital for neural crest development.
Purpose of the Study:
- Investigate the role of the foxd3 gene in zebrafish neural crest development.
- Determine how foxd3 influences neural crest cell specification, migration, and survival.
- Identify downstream targets regulated by foxd3.
Main Methods:
- Analysis of zebrafish sympathetic mutation 1 (sym1) mutants.
- Gene expression analysis of snai1b and sox10.
- TUNEL assay to detect apoptosis.
- Observation of neural crest cell migration patterns.
Main Results:
- sym1 mutants exhibit defects in peripheral neurons, glia, and cartilage, but not melanocytes.
- foxd3 regulates snai1b and sox10 expression in premigratory neural crest cells.
- Neural crest cell migration is delayed, with reduced numbers along the medial pathway.
- Aberrant apoptosis occurs in the hindbrain neural crest of sym1 mutants.
Conclusions:
- foxd3 is essential for specifying premigratory neural crest cells towards neuronal, glial, or cartilage fates.
- foxd3 regulates lineage-associated transcription factors and subsequent cell migration.
- foxd3 plays a critical role in the survival of specific neural crest cell subpopulations.
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