Direct Mapping of Cytomechanical Homeostasis Destruction in Osteoarthritis Based on Silicon Nanopillar Array

Author:

Yu Dengjie12,Nie Qingbin3,Xue Jiangtao24,Luo Ruizeng2,Xie Shiwang2,Chao Shengyu2,Wang Engui2,Xu Linlin25,Shan Yizhu2,Liu Zhuo26,Li Yusheng1,Li Zhou27ORCID

Affiliation:

1. Department of Orthopedics Xiangya hospital National Clinical Research Center for Geriatric Disorders Xiangya Hospital Central South University Changsha 410008 China

2. Beijing Institute of Nanoenergy and Nanosystems Chinese Academy of Sciences Beijing 101400 China

3. Department of Neurosurgery PLA General Hospital Beijing 100853 China

4. School of Medical Technology Beijing Institute of Technology Beijing 100081 China

5. CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety & CAS Center for Excellence in Nanoscience National Center for Nanoscience and Technology of China Beijing 100190 China

6. Key Laboratory of Biomechanics and Mechanobiology Ministry of Education Beijing Advanced Innovation Center for Biomedical Engineering School of Engineering Medicine Beihang University Beijing 100191 China

7. Institute for Stem Cell and Regeneration Chinese Academy of Sciences Beijing 100101 China

Abstract

AbstractOsteoarthritis (OA) is the most prevalent joint degenerative disease characterized by chronic joint inflammation. The pathogenesis of OA has not been fully elucidated yet. Cartilage erosion is the most significant pathological feature in OA, which is considered the result of cytomechanical homeostasis destruction. The cytomechanical homeostasis is maintained by the dynamic interaction between cells and the extracellular matrix, which can be reflected by cell traction force (CTF). It is critical to assess the CTF to provide a deeper understanding of the cytomechanical homeostasis destruction and progression in OA. In this study, a silicon nanopillar array (Si‐NP) with high spatial resolution and aspect ratio is fabricated to investigate the CTF in response to OA. It is discovered that the CTF is degraded in OA, which is attributed to the F‐actin reorganization induced by the activation of RhoA/ROCK signaling pathway. Si‐NP also shows promising potential as a mechanopharmacological assessment platform for OA drug screening and evaluation.

Funder

National Key Research and Development Program of China

Natural Science Foundation of Beijing Municipality

National Natural Science Foundation of China

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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