3.9 Review

Transgenic Mouse Models of Alzheimer's Disease

Journal

MOUNT SINAI JOURNAL OF MEDICINE
Volume 77, Issue 1, Pages 69-81

Publisher

JOHN WILEY & SONS INC
DOI: 10.1002/msj.20159

Keywords

Alzheimer's disease; amyloid precursor protein; animal model; presenilins; transgenic mice

Funding

  1. National Institute on Aging [AG20139, AG029361, AG02219, AG05138]
  2. Alzheimer's Association [IIRG-07-57318]
  3. Department of Veterans Affairs [1101BX000342]
  4. NATIONAL INSTITUTE ON AGING [P01AG002219, F32AG005875, R01AG020139, P50AG005138, R21AG029361] Funding Source: NIH RePORTER
  5. Veterans Affairs [I01BX000342] Funding Source: NIH RePORTER

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Alzheimer's disease is the most common cause of senile dementia in the United States and Europe. At present, there is no effective treatment. Given the disease's prevalence and poor prognosis, the development of animal models has been a high research priority. Transgenic modeling has been pursued oil the basis of the amyloid hypothesis and has taken advantage Of mutations in the amyloid precursor protein and the presenilins that cause familial forms of Alzheimer's disease. Modeling has been most aggressively pursued in mice, for which the techniques of genetic modification are well developed Transgenic mouse models now exist that mimic a range of Alzheimer's disease-related p pathologies. Although none of the models fully replicates the human disease, the models have contributed significant insights into the pathophysiology of beta-amyloid toxicity, particularly with respect to the effects of: different beta-amyloid species and the possible pathogenic role of beta-amyloid oligomers. They have also been widely used in the preclinical testing of potential therapeutic modalities and have played a pivotal role in the development of immunotherapies for Alzheimer's disease that are currently ill clinical trials. These models Will, without a doubt, continue to Play central roles in preclinical testing and be used as tools for developing insights into the biological basis of Alzheimer's disease. Mt Sinai J Med 77:69-81, 2010. (C) 2010 Mount Sinai School of Medicine

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