Academic Journal
Nano‐Brake Halts Mitochondrial Dysfunction Cascade to Alleviate Neuropathology and Rescue Alzheimer's Cognitive Deficits
العنوان: | Nano‐Brake Halts Mitochondrial Dysfunction Cascade to Alleviate Neuropathology and Rescue Alzheimer's Cognitive Deficits |
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المؤلفون: | Zhang, Qian, Song, Qingxiang, Yu, Renhe, Wang, Antian, Jiang, Gan, Huang, Yukun, Chen, Jun, Xu, Jianrong, Wang, Dayuan, Chen, Hongzhuan, Gao, Xiaoling |
المساهمون: | National Natural Science Foundation of China, Science and Technology Commission of Shanghai Municipality, China Postdoctoral Science Foundation |
المصدر: | Advanced Science ; volume 10, issue 7 ; ISSN 2198-3844 2198-3844 |
بيانات النشر: | Wiley |
سنة النشر: | 2023 |
المجموعة: | Wiley Online Library (Open Access Articles via Crossref) |
الوصف: | Mitochondrial dysfunction has been recognized as the key pathogenesis of most neurodegenerative diseases including Alzheimer's disease (AD). The dysregulation of mitochondrial calcium ion (Ca 2+ ) homeostasis and the mitochondrial permeability transition pore (mPTP), is a critical upstream signaling pathway that contributes to the mitochondrial dysfunction cascade in AD pathogenesis. Herein, a “two‐hit braking” therapeutic strategy to synergistically halt mitochondrial Ca 2+ overload and mPTP opening to put the mitochondrial dysfunction cascade on a brake is proposed. To achieve this goal, magnesium ion (Mg 2+ ), a natural Ca 2+ antagonist, and siRNA to the central mPTP regulator cyclophilin D (CypD), are co‐encapsulated into the designed nano‐brake; A matrix metalloproteinase 9 (MMP9) activatable cell‐penetrating peptide (MAP) is anchored on the surface of nano‐brake to overcome the blood‐brain barrier (BBB) and realize targeted delivery to the mitochondrial dysfunction cells of the brain. Nano‐brake treatment efficiently halts the mitochondrial dysfunction cascade in the cerebrovascular endothelial cells, neurons, and microglia and powerfully alleviates AD neuropathology and rescues cognitive deficits. These findings collectively demonstrate the potential of advanced design of nanotherapeutics to halt the key upstream signaling pathways of mitochondrial dysfunction to provide a powerful strategy for AD modifying therapy. |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | English |
DOI: | 10.1002/advs.202204596 |
الاتاحة: | http://dx.doi.org/10.1002/advs.202204596 https://onlinelibrary.wiley.com/doi/pdf/10.1002/advs.202204596 https://onlinelibrary.wiley.com/doi/full-xml/10.1002/advs.202204596 |
Rights: | http://creativecommons.org/licenses/by/4.0/ |
رقم الانضمام: | edsbas.D72916C8 |
قاعدة البيانات: | BASE |
DOI: | 10.1002/advs.202204596 |
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