WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

The Journal of Neuroscience, October 20, 2004, 24(42):9441-9450; doi:10.1523/JNEUROSCI.3290-04.2004

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
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 Web of Science (26)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Adams, S. M.
Right arrow Articles by Corriveau, R. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Adams, S. M.
Right arrow Articles by Corriveau, R. A.

 Previous Article  |  Next Article 

Development/Plasticity/Repair
Pronounced Cell Death in the Absence of NMDA Receptors in the Developing Somatosensory Thalamus

Suzanne M. Adams,1 * Juan Carlos de Rivero Vaccari,2 * and Roderick A. Corriveau2

1Department of Anatomy and Cell Biology, Wayne State University, Detroit, Michigan 48201, and 2Department of Cell Biology and Anatomy, Louisiana State University Health Science Center, New Orleans, Louisiana 70112

Genetic deletion of NMDA glutamate receptors disrupts development of whisker-related neuronal patterns in the somatosensory system. Independent studies have shown that NMDA receptor antagonists increase cell death among developing neurons. Here, we report that a dramatic feature of the developing somatosensory system in newborn NMDA receptor 1 (NMDAR1) knock-out mice is increased cell death in the ventrobasal nucleus (VB) of the thalamus. Sections were subject to terminal deoxynucleotidyl transferase dUTP nick end labeling staining for apoptotic DNA fragmentation, thionine staining for pyknotic nuclei, silver staining for degenerating cells, and immunostaining for caspase-3. All four methods demonstrated that deletion of NMDAR1 causes a large (on the order of threefold to fivefold) increase in cell death in the VB. The NMDA receptor antagonists dizocilpine maleate (MK-801) and phencyclidine also increase cell death in this structure. The onset of increased cell death in the VB in the absence of NMDA receptor function is approximately the time of birth, overlaps with naturally occurring cell death and synaptogenesis, and displays some anatomical specificity. For example, there was no increase in cell death in the hippocampus or neocortex of NMDAR1 knock-out mice at any of the time points examined: embryonic day 15.5 (E15.5), E17.5, and postnatal day 0. We also report a significant reduction in the size of the VB that is evident starting at E17.5. The results indicate that NMDA receptors play a major role in cell survival during naturally occurring cell death in the VB and demonstrate that cell death is a consideration in NMDA receptor knock-out studies.

Key words: development; NMDA receptor; somatosensory; thalamus; cell death; apoptosis


Received May 26, 2003; revised September 10, 2004; accepted September 11, 2004.




This article has been cited by other articles:


Home page
J. Neurosci.Home page
F. X. Soriano, M.-A. Martel, S. Papadia, A. Vaslin, P. Baxter, C. Rickman, J. Forder, M. Tymianski, R. Duncan, M. Aarts, et al.
Specific Targeting of Pro-Death NMDA Receptor Signals with Differing Reliance on the NR2B PDZ Ligand
J. Neurosci., October 15, 2008; 28(42): 10696 - 10710.
[Abstract] [Full Text] [PDF]


Home page
Cereb CortexHome page
N. Heck, A. Golbs, T. Riedemann, J.-J. Sun, V. Lessmann, and H. J. Luhmann
Activity-Dependent Regulation of Neuronal Apoptosis in Neonatal Mouse Cerebral Cortex
Cereb Cortex, June 1, 2008; 18(6): 1335 - 1349.
[Abstract] [Full Text] [PDF]


Home page
NeuroscientistHome page
S. Papadia and G. E. Hardingham
The Dichotomy of NMDA Receptor Signaling
Neuroscientist, December 1, 2007; 13(6): 572 - 579.
[Abstract] [PDF]


Home page
J. Neurophysiol.Home page
J. C. de Rivero Vaccari, R. A. Corriveau, and A. B. Belousov
Gap Junctions Are Required for NMDA Receptor Dependent Cell Death in Developing Neurons
J Neurophysiol, November 1, 2007; 98(5): 2878 - 2886.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
F. X. Soriano and G. E. Hardingham
Compartmentalized NMDA receptor signalling to survival and death
J. Physiol., October 15, 2007; 584(2): 381 - 387.
[Abstract] [Full Text] [PDF]


Home page
Mol. Interv.Home page
L. K. Friedman
CALCIUM: A Role for Neuroprotection and Sustained Adaptation
Mol. Interv., December 1, 2006; 6(6): 315 - 329.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. C. de Rivero Vaccari, G. P. Casey, S. Aleem, W.-M. Park, and R. A. Corriveau
NMDA receptors promote survival in somatosensory relay nuclei by inhibiting Bax-dependent developmental cell death
PNAS, November 7, 2006; 103(45): 16971 - 16976.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
F. X. Soriano, S. Papadia, F. Hofmann, N. R. Hardingham, H. Bading, and G. E. Hardingham
Preconditioning doses of NMDA promote neuroprotection by enhancing neuronal excitability.
J. Neurosci., April 26, 2006; 26(17): 4509 - 4518.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
P. Lachamp, B. Balland, F. Tell, A. Baude, C. Strube, M. Crest, and J.-P. Kessler
Early expression of AMPA receptors and lack of NMDA receptors in developing rat climbing fibre synapses
J. Physiol., May 1, 2005; 564(3): 751 - 763.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
S. Papadia, P. Stevenson, N. R. Hardingham, H. Bading, and G. E. Hardingham
Nuclear Ca2+ and the cAMP Response Element-Binding Protein Family Mediate a Late Phase of Activity-Dependent Neuroprotection
J. Neurosci., April 27, 2005; 25(17): 4279 - 4287.
[Abstract] [Full Text] [PDF]



-
-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2009 by Society for Neuroscience ONLINE ISSN: 1529-2401
-