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Utilization of APPswe/PS1dE9 Transgenic Mice in Research of Alzheimer′s Disease: Focus on Gene Therapy and Cell‐Based Therapy Applications
Author(s) -
Tarja Malm,
Jari Koıstınaho,
Katja M. Kanninen
Publication year - 2011
Publication title -
international journal of alzheimer s disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.657
H-Index - 49
eISSN - 2090-8024
pISSN - 2090-0252
DOI - 10.4061/2011/517160
Subject(s) - genetic enhancement , transgene , genetically modified mouse , disease , focus (optics) , neuroscience , medicine , gene , psychology , biology , pathology , biochemistry , physics , optics
One of the most extensively used transgenic mouse model of Alzheimer's disease (AD) is APPswe/PS1dE9 mice, which over express the Swedish mutation of APP together with PS1 deleted in exon 9. These mice show increase in parenchymal A β load with A β plaques starting from the age of four months, glial activation, and deficits in cognitive functions at the age of 6 months demonstrated by radial arm water maze and 12-13 months seen with Morris Water Maze test. As gene transfer technology allows the delivery of DNA into target cells to achieve the expression of a protective or therapeutic protein, and stem cell transplantation may create an environment supporting neuronal functions and clearing A β plaques, these therapeutic approaches alone or in combination represent potential therapeutic strategies that need to be tested in relevant animal models before testing in clinics. Here we review the current utilization of APPswe/PS1dE9 mice in testing gene transfer and cell transplantation aimed at improving the protection of the neurons against A β toxicity and also reducing the brain levels of A β . Both gene therapy and cell based therapy may be feasible therapeutic approaches for human AD.

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