SSK1‐Loaded Neurotransmitter‐Derived Nanoparticles for Alzheimer's Disease Therapy via Clearance of Senescent Cells

Author:

Ji Wenbo1,Zhou Honglei2,Liang Wendanqi13,Zhang Weicong4,Gong Baofeng1,Yin Tong1,Chu Jianjian1,Zhuang Jianhua1,Zhang Jian5,Luo Yi56,Liu Yan5,Gao Jie7,Yin You18ORCID

Affiliation:

1. Department of Neurology Second Afffliated Hospital (Shanghai Changzheng Hospital) of Naval Medical University Fengyang Road, Huangpu District Shanghai 200003 China

2. Department of General Surgery The First Affiliated Hospital with Nanjing Medical University Changle Road, Qinhuai District Nanjing 210006 China

3. School of Health Science and Engineering University of Shanghai for Science and Technology Jungong Road, Yangpu District Shanghai 200093 China

4. School of Pharmacy University College London Gower Street London W12 8LP UK

5. Department of Clinical Pharmacy Xinhua Hospital Shanghai Jiao Tong University School of Medicine Clinical Pharmacy Innovatton Instttute Shanghai Jiao Tong University School of Medicine Kongjiang Road, Yangpu District Shanghai 200092 China

6. New Drug Discovery and Development Biotheus Inc Keji 7th Road, TangjiawanTown Zhuhai 519080 China

7. Changhai Clinical Research Unit Shanghai Changhai Hospital Naval Medical University Changhai Road, Yangpu District Shanghai 200433 China

8. Department of Neurology Shanghai East Hospital School of Medicine Tongji University Jimo Road, Pudong New District Shanghai 200120 China

Abstract

AbstractAge is a significant contributor to the onset of AD. Senolysis has been recently demonstrated to ameliorate aging‐associated diseases that showing a great potential in AD therapy. However, due to the presence of BBB, the anti‐AD activity of senolytics are significantly diminished. SSK1 is a prodrug that can be activated by β‐gal, a lysosomal enzyme commonly upregulated in senescent cells, and thus selectively eliminates senescent cells. Furthermore, the level of β‐gal is significantly correlated with conventional AD genes from clinical sequencing data. SSK1‐loaded neurotransmitter ‐derived lipid nanoparticles are herein developed (SSK1‐NPs) that revealing good BBB penetration and bioavailability of in the body. At the brain lesion, SSK1‐NP treatment significantly reduces the expression of genes associated with senescence, induced senescent cells elimination, decreased amyloid‐beta accumulation, and eventually improve cognitive function of aged AD mice. SSK1‐NPs, a novel nanomedicine displaying potent anti‐AD activity and excellent safety profile, provides a promising strategy for AD therapy.

Funder

Natural Science Foundation of Shanghai Municipality

Publisher

Wiley

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