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Published December 15, 2007 | Accepted Version
Journal Article Open

A critical role for Cadherin6B in regulating avian neural crest emigration

Abstract

Neural crest cells originate in the dorsal neural tube but subsequently undergo an epithelial-to-mesenchymal transition (EMT), delaminate, and migrate to diverse locations in the embryo where they contribute to a variety of derivatives. Cadherins are a family of cell–cell adhesion molecules expressed in a broad range of embryonic tissues, including the neural tube. In particular, cadherin6B (Cad6B) is expressed in the dorsal neural tube prior to neural crest emigration but is then repressed by the transcription factor Snail2, expressed by premigratory and early migrating cranial neural crest cells. To examine the role of Cad6B during neural crest EMT, we have perturbed Cad6B protein levels in the cranial neural crest-forming region and have examined subsequent effects on emigration and migration. The results show that knock-down of Cad6B leads to premature neural crest cell emigration, whereas Cad6B overexpression disrupts migration. Our data reveal a novel role for Cad6B in controlling the proper timing of neural crest emigration and delamination from the neural tube of the avian embryo.

Additional Information

© 2007 Elsevier Inc. Received for publication 24 May 2007; revised 27 September 2007; accepted 27 September 2007. Available online 5 October 2007. We thank Dr. Stephen Price for the full-length Cad6B plasmid that was used as a PCR template and David Arce for excellent technical assistance. This work was supported by grants from the American Heart Association (0525037Y to EGC), NIH-NICHD (K99-HD055034 to LAT) and NIH (NS36585 to MBF).

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August 22, 2023
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