spacer gif spacer gif spacer gif spacer gif ARCHIVE ANNOUNCEMENT! spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

doi: 10.1242/10.1242/dev.00569


This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lyons, D. A.
Right arrow Articles by Clarke, J. D. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lyons, D. A.
Right arrow Articles by Clarke, J. D. W.
Development 130, 3427-3436 (2003)
Copyright © 2003 The Company of Biologists Limited

Monitoring neural progenitor fate through multiple rounds of division in an intact vertebrate brain

David A. Lyons, Adam T. Guy and Jonathan D. W. Clarke*

Centre for Cellular and Molecular Dynamics, Department of Anatomy and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK

* Author for correspondence (e-mail: jonathan.clarke{at}ucl.ac.uk)

Accepted 25 April 2003

The behaviour of neural progenitors in the intact vertebrate brain and spinal cord is poorly understood, chiefly because of the inaccessibility and poor optical qualities inherent in many model systems. To overcome these problems we have studied the optically superior brain of the zebrafish embryo and have monitored the in vivo behaviour of fluorescently labelled neural progenitors and their daughter cells throughout a substantial period of hindbrain development. We find the majority (84%) of hindbrain neurons are born from progenitor divisions that generate two neurons and 68% of reconstructed lineage trees contained no asymmetric stem cell-like divisions. No progenitors divided in the manner expected of a classic stem cell; i.e. one that repeatedly self-renews and generates a differentiated cell type by asymmetric division. We also analysed the orientation of progenitor divisions relative to the plane of the ventricular zone (VZ) and find that this does not correlate with the fate of the daughter cells. Our results suggest that in this vertebrate system the molecular determinants that control whether a cell will become a neuron are usually not linked to a mechanism that generates asymmetric divisions.

Key words: In vivo imaging, Vertebrate neurogenesis, Neural progenitor cell fate, Asymmetric division, Zebrafish




This article has been cited by other articles:


Home page
J. Neurosci.Home page
D. Delaunay, K. Heydon, A. Cumano, M. H. Schwab, J.-L. Thomas, U. Suter, K.-A. Nave, B. Zalc, and N. Spassky
Early Neuronal and Glial Fate Restriction of Embryonic Neural Stem Cells
J. Neurosci., March 5, 2008; 28(10): 2551 - 2562.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
M. R. Costa, G. Wen, A. Lepier, T. Schroeder, and M. Gotz
Par-complex proteins promote proliferative progenitor divisions in the developing mouse cerebral cortex
Development, January 1, 2008; 135(1): 11 - 22.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
L. M. Baye and B. A. Link
Interkinetic Nuclear Migration and the Selection of Neurogenic Cell Divisions during Vertebrate Retinogenesis
J. Neurosci., September 19, 2007; 27(38): 10143 - 10152.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
A. C. Wilcock, J. R. Swedlow, and K. G. Storey
Mitotic spindle orientation distinguishes stem cell and terminal modes of neuron production in the early spinal cord
Development, May 15, 2007; 134(10): 1943 - 1954.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J. Battiste, A. W. Helms, E. J. Kim, T. K. Savage, D. C. Lagace, C. D. Mandyam, A. J. Eisch, G. Miyoshi, and J. E. Johnson
Ascl1 defines sequentially generated lineage-restricted neuronal and oligodendrocyte precursor cells in the spinal cord
Development, January 15, 2007; 134(2): 285 - 293.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J. G. Crump, M. E. Swartz, J. K. Eberhart, and C. B. Kimmel
Moz-dependent Hox expression controls segment-specific fate maps of skeletal precursors in the face
Development, July 15, 2006; 133(14): 2661 - 2669.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
S. Wu, Y. Wu, and M. R. Capecchi
Motoneurons and oligodendrocytes are sequentially generated from neural stem cells but do not appear to share common lineage-restricted progenitors in vivo
Development, February 15, 2006; 133(4): 581 - 590.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Biol.Home page
L. Poggi, M. Vitorino, I. Masai, and W. A. Harris
Influences on neural lineage and mode of division in the zebrafish retina in vivo
J. Cell Biol., December 19, 2005; 171(6): 991 - 999.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
C. L. Bladen, W. K. Lam, W. S. Dynan, and D. J. Kozlowski
DNA damage response and Ku80 function in the vertebrate embryo
Nucleic Acids Res., May 24, 2005; 33(9): 3002 - 3010.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2003