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Loss of presenilin function causes impairments of memory and synaptic plasticity followed by age-dependent neurodegeneration.

Mutations in presenilins are the major cause of familial Alzheimer's disease, but the pathogenic mechanism by which presenilin mutations cause memory loss and neurodegeneration remains unclear. Here we demonstrate that conditional double knockout mice lacking both presenilins in the postnatal forebrain exhibit impairments in hippocampal memory and synaptic plasticity. These deficits are associated with specific reductions in NMDA receptor-mediated responses and synaptic levels of NMDA receptors and alphaCaMKII. Furthermore, loss of presenilins causes reduced expression of CBP and CREB/CBP target genes, such as c-fos and BDNF. With increasing age, mutant mice develop striking neurodegeneration of the cerebral cortex and worsening impairments of memory and synaptic function. Neurodegeneration is accompanied by increased levels of the Cdk5 activator p25 and hyperphosphorylated tau. These results define essential roles and molecular targets of presenilins in synaptic plasticity, learning and memory, and neuronal survival in the adult cerebral cortex.

Pubmed ID: 15066262

Authors

  • Saura CA
  • Choi SY
  • Beglopoulos V
  • Malkani S
  • Zhang D
  • Shankaranarayana Rao BS
  • Chattarji S
  • Kelleher RJ
  • Kandel ER
  • Duff K
  • Kirkwood A
  • Shen J

Journal

Neuron

Publication Data

April 8, 2004

Associated Grants

  • Agency: NINDS NIH HHS, Id: NS41783

Mesh Terms

  • Activating Transcription Factor 1
  • Age Factors
  • Animals
  • Antibodies, Monoclonal
  • Association Learning
  • Behavior, Animal
  • Blotting, Western
  • Brain
  • Calcium-Calmodulin-Dependent Protein Kinase Kinase
  • Carrier Proteins
  • Cyclin-Dependent Kinase 5
  • Cyclin-Dependent Kinases
  • DNA-Binding Proteins
  • Disease Models, Animal
  • Excitatory Amino Acid Agonists
  • Fear
  • Gene Expression Regulation
  • Gene Products, gag
  • Immunohistochemistry
  • In Vitro Techniques
  • Lamin Type B
  • Long-Term Potentiation
  • Membrane Potentials
  • Membrane Proteins
  • Memory Disorders
  • Mice
  • Mice, Knockout
  • Microtubule-Associated Proteins
  • N-Methylaspartate
  • Neurodegenerative Diseases
  • Neuronal Plasticity
  • Patch-Clamp Techniques
  • Precipitin Tests
  • Presenilin-1
  • Protein-Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-fos
  • RNA, Messenger
  • Reaction Time
  • Receptors, N-Methyl-D-Aspartate
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Transcription Factors
  • Viral Proteins
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid
  • gag Gene Products, Human Immunodeficiency Virus