ApoE worsens neurodegeneration caused by aggregating tau proteins | September 25, 2017 Issue - Vol. 95 Issue 38 | Chemical & Engineering News
Volume 95 Issue 38 | p. 9 | Concentrates
Issue Date: September 25, 2017

ApoE worsens neurodegeneration caused by aggregating tau proteins

Findings in mice provide further insight into the mechanism behind the greatest genetic risk factor for Alzheimer’s disease
Department: Science & Technology
News Channels: Biological SCENE
Keywords: Neuroscience, Alzheimer's disease, ApoE, tau, protein aggregation
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Mice carrying the ApoE4 gene (left) had greater loss of brain tissue caused by aggregating tau protein compared with animals without ApoE (right). Each brain slice is about 5 mm wide.
Credit: Yang Shi/Washington University School of Medicine
Two slices of mouse brains showing how ApoE enhances tissue loss caused by aggregating tau.
 
Mice carrying the ApoE4 gene (left) had greater loss of brain tissue caused by aggregating tau protein compared with animals without ApoE (right). Each brain slice is about 5 mm wide.
Credit: Yang Shi/Washington University School of Medicine

The greatest genetic risk factor for Alzheimer’s disease is carrying the E4 version of the gene ApoE, which codes for apolipoprotein E. People with two copies of ApoE4 have a 12-fold increased risk of developing the neurodegenerative disease, says David M. Holtzman of Washington University School of Medicine in St. Louis. Most research into the mechanism connecting ApoE and Alzheimer’s has focused on how the protein increases deposition of amyloid-β, the main protein that aggregates and forms clumps in the brains of people with the disease. Holtzman and colleagues now report that, in mice, ApoE also enhances the damage caused by tau, the other aggregating protein linked to Alzheimer’s (Nature 2017, DOI: 10.1038/nature24016). The findings suggest that knocking down expression of ApoE could slow the progression of neurodegeneration. The scientists studied mice engineered to produce a mutated version of tau that is prone to aggregate. They then bred those mice with other mice that express one or none of the three versions of the human ApoEgene. Of the resulting offspring, the mice carrying ApoE4 had the highest tau levels throughout the brain, as well as the greatest loss of brain tissue. Mice without ApoE still had tau accumulation but almost no tissue loss. The scientists think ApoE enhances a damaging inflammatory response triggered by the tau tangles.

 
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