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Updated: Jun 10, 2026

Assaying β-amyloid Toxicity using a Transgenic C. elegans Model
Published on: October 9, 2010
Bacteria-derived equol alleviates Aβ toxicity in C. elegans through PEK-1-associated UPRer activation
Wei Yao1, Mingqin Qu1, Cui Deng1
1Department of Cell Biology, School of Basic Medical Sciences, Laboratory for Clinical Medicine, Capital Medical University, Beijing, 100069, China.
None:
Alzheimer's disease (AD) is the leading cause of dementia with no effective disease-modifying treatments. Here, we found that Escherichia coli (E. coli) DH5α relieved learning defects and paralysis, and prolonged lifespan in amyloid-β (Aβ)-expressing C. elegans. DH5α inhibited Aβ aggregation via activating the PEK-1-dependent endoplasmic reticulum unfolded protein response (UPRer). We further identified equol from DH5α metabolites, which alleviated AD-related phenotypes through the same PEK-1/UPRer pathway.

