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A critical function for beta-amyloid precursor protein in neuronal migration revealed by in utero RNA interference.

Authors: Young-Pearse, TL  Bai, J  Chang, R  Zheng, JB  LoTurco, JJ  Selkoe, DJ 
Citation: Young-Pearse TL, etal., J Neurosci. 2007 Dec 26;27(52):14459-69.
Pubmed: (View Article at PubMed) PMID:18160654
DOI: Full-text: DOI:10.1523/JNEUROSCI.4701-07.2007

Physiological processing of the beta-amyloid precursor protein (APP) generates amyloid beta-protein, which can assemble into oligomers that mediate synaptic failure in Alzheimer's disease. Two decades of research have led to human trials of compounds that chronically target this processing, and yet the normal function of APP in vivo remains unclear. We used the method of in utero electroporation of shRNA constructs into the developing cortex to acutely knock down APP in rodents. This approach revealed that neuronal precursor cells in embryonic cortex require APP to migrate correctly into the nascent cortical plate. cDNAs encoding human APP or its homologues, amyloid precursor-like protein 1 (APLP1) or APLP2, fully rescued the shRNA-mediated migration defect. Analysis of an array of mutations and deletions in APP revealed that both the extracellular and cytoplasmic domains of APP are required for efficient rescue. Whereas knock-down of APP inhibited cortical plate entry, overexpression of APP caused accelerated migration of cells past the cortical plate boundary, confirming that normal APP levels are required for correct neuronal migration. In addition, we found that Disabled-1 (Dab1), an adaptor protein with a well established role in cortical cell migration, acts downstream of APP for this function in cortical plate entry. We conclude that full-length APP functions as an important factor for proper migration of neuronal precursors into the cortical plate during the development of the mammalian brain.


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CRRD Object Information
CRRD ID: 2324689
Created: 2010-05-11
Species: All species
Last Modified: 2010-05-11
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.