 |
The Journal of Neuroscience, December 27, 2006, 26(52):13428-13436; doi:10.1523/JNEUROSCI.4180-06.2006
Previous Article | Next Article 
Neurobiology of Disease
Deficits in Synaptic Transmission and Learning in Amyloid Precursor Protein (APP) Transgenic Mice Require C-Terminal Cleavage of APP
Michael J. Saganich,1 *
Brock E. Schroeder,2 *
Veronica Galvan,3
Dale E. Bredesen,3
Edward H. Koo,2 and
Stephen F. Heinemann1
1Salk Institute for Biological Studies, La Jolla, California 92037, 2Department of Neurosciences, University of California at San Diego, La Jolla, California 92037, and 3Buck Institute for Age Research, Novato, California 94945
Correspondence should be addressed to Dr. Michael J. Saganich, Salk Institute for Biological Sciences, 10010 North Torrey Pines Road, La Jolla, CA 92037. Email: saganich{at}salk.edu
Synaptic dysfunction has been shown to be one of the earliest correlates of disease progression in animal models of Alzheimer's disease. Amyloid-ß protein (Aß) is thought to play an important role in disease-related synaptic dysfunction, but the mechanism by which Aß leads to synaptic dysfunction is not understood. Here we describe evidence that cleavage of APP in the C terminus may be necessary for the deficits present in APP transgenic mice. In APP transgenic mice with a mutated cleavage site at amino acid 664, normal synaptic transmission, synaptic plasticity, and learning were maintained despite the presence of elevated levels of APP, Aß42, and even plaque accumulation. These results indicate that cleavage of APP may play a critical role in the development of synaptic and behavioral dysfunction in APP transgenic mice.
Key words: Aß-peptide; potentiation; Schaffer collateral terminals; synaptic plasticity; hippocampus; learning memory; spatial memory; LTP; amyloid; Alzheimer's disease
Received May 15, 2006;
revised Nov. 13, 2006;
accepted Nov. 16, 2006.
Correspondence should be addressed to Dr. Michael J. Saganich, Salk Institute for Biological Sciences, 10010 North Torrey Pines Road, La Jolla, CA 92037. Email: saganich{at}salk.edu
This article has been cited by other articles:

|
 |

|
 |
 
G. Dziewczapolski, C. M. Glogowski, E. Masliah, and S. F. Heinemann
Deletion of the {alpha}7 Nicotinic Acetylcholine Receptor Gene Improves Cognitive Deficits and Synaptic Pathology in a Mouse Model of Alzheimer's Disease
J. Neurosci.,
July 8, 2009;
29(27):
8805 - 8815.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. Kerjan, H. Koizumi, E. B. Han, C. M. Dube, S. N. Djakovic, G. N. Patrick, T. Z. Baram, S. F. Heinemann, and J. G. Gleeson
Mice lacking doublecortin and doublecortin-like kinase 2 display altered hippocampal neuronal maturation and spontaneous seizures
PNAS,
April 21, 2009;
106(16):
6766 - 6771.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. Laifenfeld, L. J. Patzek, D. L. McPhie, Y. Chen, Y. Levites, A. M. Cataldo, and R. L. Neve
Rab5 Mediates an Amyloid Precursor Protein Signaling Pathway That Leads to Apoptosis
J. Neurosci.,
July 4, 2007;
27(27):
7141 - 7153.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|

|