Neuronal endocytic defects occur in Alzheimer's disease (AD) and Down syndrome (DS). Our previous work has characterized AD-relevant endosomal pathology in DS model systems, and has demonstrated that these endosomal changes lead to pathological dysfunction of the endocytic system and the downstream lysosomal system. This project will investigate the mechanisms of endosomal pathology in the disease, examining the role played by cholesterol and the B-cleaved C-termlnal fragment (BCTF) of the amyloid precursor protein (APP) In modulating endocytic function. With the knowledge base developed previously in this program that the endosomal defects seen in AD and DS are likely to contribute directly to neuronal vulnerability, we will determine in vivo In Aim 1 the mechanisms by which dietary fat and/or cholesterol leads to neurodegenerative changes mediated through endosomal dysfunction.
In Aim 2, our understanding of cholesteroldriven early endosomal dysfunction will be extended using primary neurons and human fibroblasts, where the response of endosomal regulatory elements and downstream lysosomal system compartments will be examined. To further our hypothesis that the BCTF of APP is a regulator of early endosomal function, and to examine potential synergy between cholesterol-driven and BCTF-driven endosomal dysfunction, we will probe this BCTF function by employing a novel system using antibodies that bind to BCTFs, increasing cellular BCTF levels. Additionally, the role of the BCTF In mediating endosomal dysfunction following dietary hyperiipidemia will be examined in vivo using BCTF-lacking BACE knockout mice. (3CTF interacting/binding partners will also be further examined in this aim. In part by using a novel X l l a transgenic mouse expressing only endogenous APP but with increased BCTFs and endosomal pathology. Lastly, in Aim 3, we will test our hypothesis that reducing endocytosis using small compound inhibitors of rab prenylation, some of which are FDA approved for other diseases, will decrease neuronal endocytic abnormalities in vivo. This project builds upon our understanding that AD-related endocytic dysfunction Is pathological, can lead to neuronal compromise, and is an important, and potentially mailable, therapeutic target.

Public Health Relevance

Findings from our group and others have established that the endosomal system is a key cellular system disrupted in neurons during Alzheimer's disease and Down syndrome. The studies proposed In this application will allow us to better understand the causes of endosomal dysfunction - such as cholesterol in the diet - its damaging effects on neurons, and develop novel therapeutic approaches to treat Alzheimer's disease

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG017617-13
Application #
8572260
Study Section
Special Emphasis Panel (ZAG1-ZIJ-6)
Project Start
Project End
Budget Start
2013-09-01
Budget End
2014-08-31
Support Year
13
Fiscal Year
2013
Total Cost
$228,398
Indirect Cost
$86,765
Name
Nathan Kline Institute for Psychiatric Research
Department
Type
DUNS #
167204762
City
Orangeburg
State
NY
Country
United States
Zip Code
10962
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