spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

First published online 26 May 2004
doi: 10.1242/dev.01191


Development 131, 3093-3105 (2004)
Published by The Company of Biologists 2004


This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
dev.01191v1
131/13/3093    most recent
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 Louvi, A.
Right arrow Articles by Grove, E. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Louvi, A.
Right arrow Articles by Grove, E. A.
Right arrowPubmed/NCBI databases
*Gene*GEO Profiles
*HomoloGene*UniGene
*Compound via MeSH
*Substance via MeSH
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Presenilin 1 in migration and morphogenesis in the central nervous system

Angeliki Louvi*,{dagger}, Sangram S. Sisodia and Elizabeth A. Grove

Department of Neurobiology, Pharmacology and Physiology, University of Chicago, 947 E. 58th Street, Chicago, IL 60637, USA

{dagger} Author for correspondence (e-mail: angeliki.louvi{at}yale.edu)

Accepted 24 March 2004

Morphogenesis of the central nervous system relies in large part upon the correct migration of neuronal cells from birthplace to final position. Two general modes of migration govern CNS morphogenesis: radial, which is mostly glia-guided and topologically relatively simple; and tangential, which often involves complex movement of neurons in more than one direction. We describe the consequences of loss of function of presenilin 1 on these fundamental processes. Previous studies of the central nervous system in presenilin 1 homozygote mutant embryos identified a premature neuronal differentiation that is transient and localized, with cortical dysplasia at later stages. We document widespread effects on CNS morphogenesis that appear strongly linked to defective neuronal migration. Loss of presenilin 1 function perturbs both radial and tangential migration in cerebral cortex, and several tangential migratory pathways in the brainstem. The inability of cells to execute their migratory trajectories affects cortical lamination, formation of the facial branchiomotor nucleus, the spread of cerebellar granule cell precursors to form the external granule layer and development of the pontine nuclei. Finally, overall morphogenesis of the mid-hindbrain region is abnormal, resulting in incomplete midline fusion of the cerebellum and overgrowth of the caudal midbrain. These observations indicate that in the absence of presenilin 1 function, the ability of a cell to move can be severely impaired regardless of its mode of migration, and, at a grosser level, brain morphogenesis is perturbed. Our results demonstrate that presenilin 1 plays a much more important role in brain development than has been assumed, consistent with a pleiotropic involvement of this molecule in cellular signaling.

Key words: Presenilin 1, Neuronal migration, Morphogenesis, Cortical development, Midbrain, Dopaminergic neurons, Cerebellum, Precerebellar nuclei, Facial branchiomotor neurons, {gamma}-Secretase, Mouse


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
Cereb CortexHome page
O. Reiner, A. Shmueli, and T. Sapir
Neuronal Migration and Neurodegeneration: 2 Sides of the Same Coin
Cereb Cortex, July 1, 2009; 19(suppl_1): i42 - i48.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
S. Ohata, S. Kinoshita, R. Aoki, H. Tanaka, H. Wada, S. Tsuruoka-Kinoshita, T. Tsuboi, S. Watabe, and H. Okamoto
Neuroepithelial cells require fucosylated glycans to guide the migration of vagus motor neuron progenitors in the developing zebrafish hindbrain
Development, May 15, 2009; 136(10): 1653 - 1663.
[Abstract] [Full Text] [PDF]


Home page
NeuroscientistHome page
M. Wines-Samuelson and J. Shen
Presenilins in the Developing, Adult, and Aging Cerebral Cortex
Neuroscientist, October 1, 2005; 11(5): 441 - 451.
[Abstract] [PDF]


Home page
DevelopmentHome page
H. A. Mason, S. M. Rakowiecki, M. Raftopoulou, S. Nery, Y. Huang, T. Gridley, and G. Fishell
Notch signaling coordinates the patterning of striatal compartments
Development, October 1, 2005; 132(19): 4247 - 4258.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
P. H. Wen, R. De Gasperi, M. A. G. Sosa, A. B. Rocher, V. L. Friedrich Jr, P. R. Hof, and G. A. Elder
Selective expression of presenilin 1 in neural progenitor cells rescues the cerebral hemorrhages and cortical lamination defects in presenilin 1-null mutant mice
Development, September 1, 2005; 132(17): 3873 - 3883.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
D. Y. Kim, L. A. M. Ingano, B. W. Carey, W. H. Pettingell, and D. M. Kovacs
Presenilin/{gamma}-Secretase-mediated Cleavage of the Voltage-gated Sodium Channel {beta}2-Subunit Regulates Cell Adhesion and Migration
J. Biol. Chem., June 17, 2005; 280(24): 23251 - 23261.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2004