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Graded potential of neural crest to form cornea, sensory neurons and cartilage along the rostrocaudal axis

Lwigale, Peter Y. and Conrad, Gary W. and Bronner, Marianne E. (2004) Graded potential of neural crest to form cornea, sensory neurons and cartilage along the rostrocaudal axis. Development, 131 (9). pp. 1979-1991. ISSN 0950-1991. http://resolver.caltech.edu/CaltechAUTHORS:LWIdev04

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Abstract

Neural crest cells arising from different rostrocaudal axial levels form different sets of derivatives as diverse as ganglia, cartilage and cornea. These variations may be due to intrinsic properties of the cell populations, different environmental factors encountered during migration or some combination thereof. We test the relative roles of intrinsic versus extrinsic factors by challenging the developmental potential of cardiac and trunk neural crest cells via transplantation into an ectopic midbrain environment. We then assess long-term survival and differentiation into diverse derivatives, including cornea, trigeminal ganglion and branchial arch cartilage. Despite their ability to migrate to the periocular region, neither cardiac nor trunk neural crest contribute appropriately to the cornea, with cardiac crest cells often forming ectopic masses on the corneal surface. Similarly, the potential of trunk and cardiac neural crest to form somatosensory neurons in the trigeminal ganglion was significantly reduced compared with control midbrain grafts. Cardiac neural crest exhibited a reduced capacity to form cartilage, contributing only nominally to Meckle's cartilage, whereas trunk neural crest formed no cartilage after transplantation, even when grafted directly into the first branchial arch. These results suggest that neural crest cells along the rostrocaudal axis display a graded loss in developmental potential to form somatosensory neurons and cartilage even after transplantation to a permissive environment. Hox gene expression was transiently maintained in the cardiac neural tube and neural crest at 12 hours post-transplantation to the midbrain, but was subsequently downregulated. This suggests that long-term differences in Hox gene expression cannot account for rostrocaudal differences in developmental potential of neural crest populations in this case.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1242/dev.01106DOIUNSPECIFIED
http://dev.biologists.org/cgi/content/abstract/131/9/1979PublisherUNSPECIFIED
Additional Information:Published by The Company of Biologists 2004. Accepted 15 January 2004. We are grateful to Dr Paul Trainor for providing us with Hoxa2 and Hoxa3 cDNA. This work was supported by the Elizabeth Ross Fellowship (to P.Y.L.), NIH-EY00952 (to G.W.C.), and DE13223 and NS36585 (to M.B.-F.).
Funders:
Funding AgencyGrant Number
Elizabeth Ross FellowshipUNSPECIFIED
National Institutes of HealthEY00952
National Institutes of HealthDE13223
National Institutes of HealthNS36585
Subject Keywords:Neural crest, Cornea, Trigeminal ganglion, Branchial arch, Quail-chick chimera
Record Number:CaltechAUTHORS:LWIdev04
Persistent URL:http://resolver.caltech.edu/CaltechAUTHORS:LWIdev04
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:12050
Collection:CaltechAUTHORS
Deposited By: Archive Administrator
Deposited On:21 Oct 2008 16:00
Last Modified:26 Dec 2012 10:26

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