Signal Converter‐Based Therapy Platform Promoting Aging Bone Healing by Improving Permeability of the Mitochondrial Membrane

Y YiYang Huang J Jiannan Mao (Department of Orthopedics First Affiliated Hospital of Soochow University Orthopedic Institute Soochow University 188 Shizi Road Suzhou Jiangsu 215006 P. R. China) Z Ziang Li W Wenbo Wang Z Zhengxia Ni (Department of Orthopedics First Affiliated Hospital of Soochow University Orthopedic Institute Soochow University 188 Shizi Road Suzhou Jiangsu 215006 P. R. China) F Feng Cai J Jincheng Tang W Wei Wang L Lichen Zhang (School of Medical Technology, Henan Key Laboratory of Immunology and Targeted Therapy, Xinxiang Medical University) L Liang Zhou X Xinzhao Jiang J Jie Wu Q Qiangqiang Guo M Min Rui (Department of Orthopedics First Affiliated Hospital of Soochow University Orthopedic Institute Soochow University 188 Shizi Road Suzhou Jiangsu 215006 P. R. China) Z Ziyan Huang (Laboratory of Behavioral Neuroscience, Institute for Quantitative Biosciences (IQB), The University of Tokyo, Tokyo, Japan.) H Haochen Jiang (School of Electronic Engineering, Xi’an University of Posts and Telecommunications 1 , Xi’an 710121, Shaanxi,) L Lingjun Wang K Kun Xi Y Yong Gu L Liang Chen

Abstract

Abstract The aging microenvironment promotes persistent inflammation and loss of intrinsic regenerative capacity. These are major obstacles to effective bone tissue repair in older adults. This study aims to explore how physical thermal stimulation can effectively delay the bone marrow mesenchymal stem cells (BMSCs) aging process. Based on this, an implantable physical signal‐converter platform is designed as a therapeutic system that enables stable heat signals at the bone injury site under ultrasound stimulation (US). It is found that the therapeutic platform controllably reduces the mitochondrial outer membrane permeabilization of aging BMSCs, bidirectionally inhibiting mitochondrial reactive oxygen species and mitochondrial DNA (mtDNA) leakage. The leakage ratio of mtDNA decreases by 22.7%. This effectively mitigates the activation of the cGAS‐STING pathway and its downstream NF‐κB signaling induced by oxidative stress in aging BMSCs, thereby attenuating the pathological advancement of chronic inflammation. Thus, it effectively restores the metabolism and osteogenic differentiation of aging BMSCs in vitro, which is further confirmed in a rat model. In the GMPG/US group, the bone mineral density increases 2–3 times at 4 weeks in the rats femoral defect model. Therefore, this ultrasound‐based signal‐conversion platform provides a promising strategy for aging bone defect repair.

Article Details

Volume / Issue Vol. 37, Issue 27
Published July 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (20)

Y

YiYang Huang

J

Jiannan Mao

Department of Orthopedics First Affiliated Hospital of Soochow University Orthopedic Institute Soochow University 188 Shizi Road Suzhou Jiangsu 215006 P. R. China

Z

Ziang Li

W

Wenbo Wang

Z

Zhengxia Ni

Department of Orthopedics First Affiliated Hospital of Soochow University Orthopedic Institute Soochow University 188 Shizi Road Suzhou Jiangsu 215006 P. R. China

F

Feng Cai

J

Jincheng Tang

W

Wei Wang

L

Lichen Zhang

School of Medical Technology, Henan Key Laboratory of Immunology and Targeted Therapy, Xinxiang Medical University

L

Liang Zhou

X

Xinzhao Jiang

J

Jie Wu

Q

Qiangqiang Guo

M

Min Rui

Department of Orthopedics First Affiliated Hospital of Soochow University Orthopedic Institute Soochow University 188 Shizi Road Suzhou Jiangsu 215006 P. R. China

Z

Ziyan Huang

Laboratory of Behavioral Neuroscience, Institute for Quantitative Biosciences (IQB), The University of Tokyo, Tokyo, Japan.

H

Haochen Jiang

School of Electronic Engineering, Xi’an University of Posts and Telecommunications 1 , Xi’an 710121, Shaanxi,

L

Lingjun Wang

K

Kun Xi

Y

Yong Gu

L

Liang Chen