Corticotrophin Releasing Factor Accelerates Neuropathology and Cognitive Decline in a Mouse Model of Alzheimer's Disease

Article type: Research Article

Authors: Dong, Hongxin^{a; *} | Murphy, Keely M.^a | Meng, Liping^a | Montalvo-Ortiz, Janitza^a | Zeng, Ziling^b | Kolber, Benedict J.^c | Zhang, Shanshan^a | Muglia, Louis J.^d | Csernansky, John G.^a

Affiliations: [a] Department of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, USA | [b] Department of Neurology, Qilu Hospital, Shandong University, Jinan, People's Republic of China | [c] Pain Center and Department of Anesthesiology, Washington University School of Medicine, St Louis, MO, USA | [d] Departments of Pediatrics and Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN, USA

Correspondence: [*] Correspondence to: Hongxin Dong, M.D., Ph.D., Assistant Professor, Department of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, 303 E. Chicago Ave, Ward 12-369, Chicago, IL 60611, USA. Tel.: +1 312 503 3433; Fax: +1 312 503 0466; E-mail: [email protected].

Abstract: Chronic stress has been suggested to influence the pathogenesis of Alzheimer's disease (AD); however, the mechanism underlying this influence remains unknown. In this study, we created a triple transgenic mouse model that overexpresses corticotrophin-releasing factor (CRF) and human amyloid-β protein precursor (AβPP), to investigate whether increases in the expression of CRF can mimic the effects of stress on amyloid metabolism and the neurodegeneration. Tg2576 mice that overexpresses human AβPP gene were crossbreed with Tetop-CRF (CRF) mice and CaMKII-tTA (tTA) mice to create a novel triple transgenic mouse model that conditioned overexpresses CRF in forebrain and overexpresses human AβPP (called AβPP+/CRF+/tTA+, or TT mice). Then we evaluated serial neuro-anatomical and behavioral phenotypes on TT mice using histological, biochemical, and behavioral assays. TT mice showed a Cushingoid-like phenotype starting at 3 months of age. At 6 months of age, these mice demonstrated increases in tissue-soluble amyloid-β (Aβ) and Aβ plaques in the cortex and hippocampus, as compared to control mice. Moreover, TT mice characterized substantial decreases in dendritic branching and dendritic spine density in pyramidal neurons in layer 4 of the frontal cortex and CA1 of the hippocampus. Finally, TT mice showed significantly impaired working memory and contextual memory, with a modest increase in anxiety-like behavior. Our results suggested genetic increases in the brain of CRF expression mimicked chronic stress on the effects of amyloid deposition, neurodegeneration, and behavioral deficits. The novel transgenic mouse model will provide a unique tool to further investigate the mechanisms between stress and AD.

Keywords: Alzheimer's disease, amyloid-β, cognitive function, corticotrophin-releasing factor, neurodegeneration, stress

DOI: 10.3233/JAD-2011-111328

Journal: Journal of Alzheimer's Disease, vol. 28, no. 3, pp. 579-592, 2012