Extracellular Matrix Remodeling Alleviates Memory Deficits in Alzheimer's Disease by Enhancing the Astrocytic Autophagy‐Lysosome Pathway

Author:

Yang Qinghu123ORCID,Yan Chengxiang12,Sun Yahan12,Xie Zhen4,Yang Liang12,Jiang Ming12,Ni Junjun4,Chen Beining35,Xu Sen12,Yuan Zhaoyue12,Wu Yanyan12,Liu Xia12,Yuan Zengqiang3ORCID,Bai Zhantao12

Affiliation:

1. School of Life Science & Research Center for Natural Peptide Drugs, Shaanxi Engineering & Technological Research Centre for Conservation & Utilization of Regional Biological Resources Yanan University Yanan 716000 China

2. Yanan Engineering & Technological Research Centre for Resource Peptide Drugs, Yanan Key Laboratory for Neural Immuno‐Tumor and Stem Cell Yanan 716000 China

3. The Brain Science Center Beijing Institute of Basic Medical Sciences Beijing 100850 China

4. Key Laboratory of Molecular Medicine and Biotherapy Department of Biology School of Life Science Beijing Institute of Technology Beijing 100081 China

5. State Key Laboratory of Reproductive Medicine, Key Laboratory of Human Functional Genomics of Jiangsu Province, Department of Neurobiology, Interdisciplinary InnoCenter for Organoids, School of Basic Medical Sciences Nanjing Medical University Nanjing 211166 China

Abstract

AbstractExtracellular matrix (ECM) remodeling is strongly linked to Alzheimer's disease (AD) risk; however, the underlying mechanisms are not fully understood. Here, it is found that the injection of chondroitinase ABC (ChABC), mimicking ECM remodeling, into the medial prefrontal cortex (mPFC) reversed short‐term memory loss and reduced amyloid‐beta (Aβ) deposition in 5xFAD mice. ECM remodeling also reactivated astrocytes, reduced the levels of aggrecan in Aβ plaques, and enhanced astrocyte recruitment to surrounding plaques. Importantly, ECM remodeling enhanced the autophagy‐lysosome pathway in astrocytes, thereby mediating Aβ clearance and alleviating AD pathology. ECM remodeling also promoted Aβ plaque phagocytosis by astrocytes by activating the astrocytic phagocytosis receptor MERTK and promoting astrocytic vesicle circulation. The study identified a cellular mechanism in which ECM remodeling activates the astrocytic autophagy‐lysosomal pathway and alleviates AD pathology. Targeting ECM remodeling may represent a potential therapeutic strategy for AD and serve as a reference for the treatment of this disease.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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