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Pharmacological targeting of MCL-1 promotes mitophagy and improves disease pathologies in an Alzheimer's disease mouse model

Medicine and Health

Pharmacological targeting of MCL-1 promotes mitophagy and improves disease pathologies in an Alzheimer's disease mouse model

X. Cen, Y. Chen, et al.

This groundbreaking study reveals the therapeutic potential of UMI-77, a drug that activates neuronal mitophagy, targeting MCL-1 as a receptor. Conducted by Xufeng Cen and colleagues, it shows promise for reversing Alzheimer’s disease symptoms through potent mitophagy activation. A game-changer in Alzheimer's treatment!

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~3 min • Beginner • English
Abstract
There is increasing evidence that inducing neuronal mitophagy can be used as a therapeutic intervention for Alzheimer’s disease. Here, we screen a library of 2024 FDA-approved drugs or drug candidates, revealing UMI-77 as an unexpected mitophagy activator. UMI-77 is an established BH3-mimetic for MCL-1 and was developed to induce apoptosis in cancer cells. We found that at sub-lethal doses, UMI-77 potently induces mitophagy, independent of apoptosis. Our mechanistic studies discovered that MCL-1 is a mitophagy receptor and directly binds to LC3A. Finally, we found that UMI-77 can induce mitophagy in vivo and that it effectively reverses molecular and behavioral phenotypes in the APP/PS1 mouse model of Alzheimer’s disease. Our findings shed light on the mechanisms of mitophagy, reveal that MCL-1 is a mitophagy receptor that can be targeted to induce mitophagy, and identify MCL-1 as a drug target for therapeutic intervention in Alzheimer’s disease.
Publisher
Nature Communications
Published On
Nov 12, 2020
Authors
Xufeng Cen, Yanying Chen, Xiaoyan Xu, Ronghai Wu, Fusheng He, Qingwei Zhao, Qiming Sun, Cong Yi, Jie Wu, Ayaz Najafov, Hongguang Xia
Tags
Alzheimer's disease
mitophagy
MCL-1
UMI-77
FDA-approved drugs
neurodegeneration
therapeutic potential
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