Published August 2007 | Version Accepted Version
Journal Article Open

Lunatic fringe causes expansion and increased neurogenesis of trunk neural tube and neural crest populations

  • 1. ROR icon California Institute of Technology

Abstract

Both neurons and glia of the PNS are derived from the neural crest. In this study, we have examined the potential function of lunatic fringe in neural tube and trunk neural crest development by gain-of-function analysis during early stages of nervous system formation. Normally lunatic fringe is expressed in three broad bands within the neural tube, and is most prominent in the dorsal neural tube containing neural crest precursors. Using retrovirally-mediated gene transfer, we find that excess lunatic fringe in the neural tube increases the numbers of neural crest cells in the migratory stream via an apparent increase in cell proliferation. In addition, lunatic fringe augments the numbers of neurons and upregulates Delta-1 expression. The results indicate that, by modulating Notch/Delta signaling, lunatic fringe not only increases cell division of neural crest precursors, but also increases the numbers of neurons in the trunk neural crest.

Additional Information

© 2007 Cambridge University Press. Received November 14 2007. Accepted November 16 2007. Published online: 06 February 2008. Special thanks to Gustavo Gomez and Ruel Velazco for their expert technical assistance and to Cindy Malone for help editing this manuscript. We thank Vivian Lee, Yun Kee and Christine Nelleman for useful discussions and Ed Laufer for providing the RCAS virus used in these experiments. This work was supported in part by a postdoctoral fellowship to MEdB from the National Multiple Sclerosis Society (FA 1383-A-1) and NIH-MBRS SCORE-5S06GM048680-13; and by a USPHS NS36585 and DE13223 to MBF.

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Additional details

Identifiers

PMCID
PMC2293300
Eprint ID
64885
Resolver ID
CaltechAUTHORS:20160301-070210885

Funding

National Multiple Sclerosis Society
FA 1383-A-1
NIH
SCORE-5S06GM048680-13
NIH
NS36585
NIH
DE13223

Dates

Created
2016-03-01
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Updated
2023-06-06
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