Elimination of Senescent Osteocytes by Bone‐Targeting Delivery of β‐Galactose‐Modified Maytansinoid Prevents Age‐Related Bone Loss

Author:

He Yi123,Zhang Lei1234,Chen Xiang123,Liu Bin123,Shao Xiaoyan123,Fang Depeng123,Lin Jiaquan123,Liu Na123,Lou Yabing5,Qin Jianghui1236,Jiang Qing1236,Guo Baosheng1236ORCID

Affiliation:

1. Division of Sports Medicine and Adult Reconstructive Surgery, Department of Orthopedic Surgery, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School Nanjing University 321 Zhongshan Road Nanjing Jiangsu 210008 P. R. China

2. State Key Laboratory of Pharmaceutical Biotechnology Nanjing University Nanjing Jiangsu 210093 P. R. China

3. Jiangsu Key Laboratory of Molecular Medicine Medical School, Nanjing University Nanjing, Jiangsu 210093 China

4. State Key Laboratory of Natural Medicines China Pharmaceutical University Nanjing 211198 P.R. China

5. Beijing Rehabilitation Hospital Capital Medical University Beijing 100069 P. R. China

6. Branch of National Clinical Research Center for Orthopedics Sports Medicine and Rehabilitation Nanjing Jiangsu 210008 P. R. China

Abstract

AbstractThe accumulation of senescent cells in bone during aging contributes to senile osteoporosis, and clearance of senescent cells by senolytics could effectively alleviate bone loss. However, the applications of senolytics are limited due to their potential toxicities. Herein, small extracellular vesicles (sEVs) have been modified by incorporating bone‐targeting peptide, specifically (AspSerSer)6, to encapsulate galactose‐modified Maytansinoids (DM1). These modified vesicles are referred to as (AspSerSer)6‐sEVs/DM1‐Gal, and they have been designed to specifically clear the senescent osteocytes in bone tissue. In addition, the elevated activity of lysosomal β‐galactosidase in senescent osteocytes, but not normal cells in bone tissue, could break down DM1‐Gal to release free DM1 for selective elimination of senescent osteocytes. Mechanically, DM1 could disrupt tubulin polymerization, subsequently inducing senescent osteocytes apoptosis. Further, administration of bone‐targeting senolytics to aged mice could alleviate aged‐related bone loss without non‐obvious toxicity. Overall, this bone‐targeting senolytics could act as a novel candidate for specific clearance of senescent osteocytes, ameliorating age‐related bone loss, with a promising therapeutic potential for senile osteoporosis.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

State Key Laboratory of Natural Medicines

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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