A Story From The Humanized Worms: Comprehensive Study Of Cellular Toxicity Of Amyloid Beta 1-42

Ning Wang, PhD
Northwestern University (Evanston, IL)

Mentors

Richard Morimoto, Ph.D.
Northwestern University
Year Awarded:
2009
Grant Duration:
April 1, 2009 to March 31, 2011
Disease:
Alzheimer's Disease
Award Amount:
$100,000
Grant Reference ID:
A2009634
Award Type:
Postdoctoral Fellowship
Award Region:
US Midwestern
Ning Wang, PhD

Compartment And Tissue Specific Toxicity Of Amyloid Beta 1-42 In C. Elegans

Summary

What is the cellular basis of amyloid beta toxicity in different cellular compartments and tissue types? What, if any, are the compartment and tissue specific signaling pathways and genetic networks that are involved in modulating amyloid beta toxicity? Is it possible to regulate these genetic networks to provide insight into therapeutic design?

Details

Alzheimer's disease (AD) is a complex aging-associated neurodegenerative disorder and is responsible for over half of all cases of dementia. It was estimated that 4.5 million persons in the U.S.A. had AD in 2000 and the number is predicted to triple by 2050 if effective therapies are not discovered. AD is characterized by accumulation of intracellular neurofibrillary tangles (NFT) of tau protein and extracellular plaques of amyloid beta1-40/1-42, which subsequently lead to neuronal degeneration. Increasing evidence indicates that the key challenge for understanding and ultimately treating AD is to focus on discovering how subtly and intermittently these misfolded proteins affect normal neuronal function, rather than focusing on later stages of disease when widespread neurodegeneration has occurred. Genetic mutations in proteins such as amyloid precursor protein (APP), ApoE4 polymorphism, presenilin 1, presenilin 2 and others have been identified in association with AD development and these mutations either enhance amyloid beta production or interfere with its clearance. The accumulation of amyloid beta has been increasingly considered to be the primary event in AD causes and development. Thus, one of the key areas of Alzheimer's disease research is to determine the cellular mechanism underneath amyloid beta toxicity. One major challenge to understanding the cellular toxicity of amyloid beta is the difficulty in accurately detecting and quantifying different pools of amyloid beta at cellular level. To systematically study the cellular toxicity of amyloid beta and identify genetic networks that are involved in modulating amyloid beta toxicity, we aim to establish a series of transgenic C. elegans models of amyloid beta1-42 expression that target the protein to different cellular compartments and different tissue types (specific aim 1). C.elegans provides a number of unique advantages making it possible to generate transgenic models comparatively easier and suitably for high-throughput testing of hypotheses. The new models proposed here will allow us to directly study cellular toxicity of amyloid beta1-42 when its expression is targeted to a specific cellular compartment or specific tissue type. Transgenic lines with a similar amyloid beta1-42 expression level will be selected and amyloid beta1-42 toxicity of different transgenic lines will be directly comparable to each other. We hope each of our models will be able to recapitulate a component of the disease stages of AD. Genetic modifiers of amyloid beta toxicity will be identified by a special technique called genomic RNAi screening (specific aim 2) to help us identify cellular factors and genetic pathways that are involved in amyloid beta toxicity, which can be potentially utilized as therapeutic targets.

Research Updates

Alzheimer's disease (AD) is a complex aging-associated neurodegenerative disorder and is responsible for over half of all cases of dementia. Increasing evidence indicates that the accumulation of beta-amyloid is the primary initiating event for AD. Although beta-amyloid plaque formation outside of nerve cells have been originally identified as a hallmark of AD, it is also important to determine how the toxicity of beta-amyloid is produced and moved around the inside of nerve cells. Dr. Ning Wang and collaborators precisely expressed beta-amyloid peptide in different cellular locations that are associated with AD.  First, Dr. Wang created a number of worm AD models that express beta-amyloid 1-40 or toxic beta-amyloid 1-42 fragments in either the body wall muscle cells or the nerve cells. The C. elegans worm is a great experimental model, because it has a small number of cells in its body with many functions similar to other organisms. The locations and amounts of beta-amyloid aggregation and corresponding cellular toxicity were determined for each model. Preliminary screens identified potential targets. The next step for Dr. Wang is to use powerful genetic tools to further characterize the specific genes and proteins that are involved in this beta-amyloid toxicity.

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