If you have an ACS member number, please enter it here so we can link this account to your membership. (optional)

ACS values your privacy. By submitting your information, you are gaining access to C&EN and subscribing to our weekly newsletter. We use the information you provide to make your reading experience better, and we will never sell your data to third party members.


Biological Chemistry

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

by Michael Torrice
September 25, 2017 | A version of this story appeared in Volume 95, Issue 38

Two slices of mouse brains showing how ApoE enhances tissue loss caused by aggregating tau.
Credit: Yang Shi/Washington University School of Medicine
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.

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.


This article has been sent to the following recipient:

Chemistry matters. Join us to get the news you need.