Programmable DNA Hydrogel Provides Suitable Microenvironment for Enhancing TSPCS Therapy in Healing of Tendinopathy

Author:

Ge Zilu12,Li Wei3,Zhao Renliang12,Xiong Wei12,Wang Dong12,Tang Yunfeng12,Fang Qian12,Deng Xiangtian12,Zhang Zhen12,Zhou Yaojia4,Chen Xiaoting4,Li Yue5,Lu Yanrong6,Wang Chengshi3,Wang Guanglin12ORCID

Affiliation:

1. Trauma Medical Center Department of Orthopaedic surgery West China Hospital Sichuan University Chengdu 610041 China

2. Department of Orthopedics Orthopedic Research Institute West China Hospital Sichuan University Chengdu 610041 China

3. Department of Endocrinology and Metabolism Center for Diabetes and Metabolism Research West China Hospital Sichuan University Chengdu 610041 China

4. Animal Experimental Center West China Hospital Sichuan University Chengdu 610041 China

5. Core Facility of West China Hospital Sichuan University Chengdu 610041 China

6. Key Laboratory of Transplant Engineering and Immunology West China Hospital Sichuan University Chengdu 610041 China

Abstract

AbstractTendon stem/progenitor cells (TSPCs) therapy is a promising strategy for enhancing cell matrix and collagen synthesis, and regulating the metabolism of the tendon microenvironment during tendon injury repair. Nevertheless, the barren microenvironment and gliding shear of tendon cause insufficient nutrition supply, damage, and aggregation of injected TSPCs around tendon tissues, which severely hinders their clinical application in tendinopathy. In this study, a TSPCs delivery system is developed by encapsulating TSPCs within a DNA hydrogel (TSPCs‐Gel) as the DNA hydrogel offers an excellent artificial extracellular matrix (ECM) microenvironment by providing nutrition for proliferation and protection against shear forces. This delivery method restricts TSPCs to the tendons, significantly extending their retention time. It is also found that TSPCs‐Gel injections can promote the healing of rat tendinopathy in vivo, where cross‐sectional area and load to failure of injured tendons in rats are significantly improved compared to the free TSPCs treatment group at 8 weeks. Furthermore, the potential healing mechanism of TSPCs‐Gel is investigated by RNA‐sequencing to identify a series of potential gene and signaling pathway targets for further clinical treatment strategies. These findings suggest the potential pathways of using DNA hydrogels as artificial ECMs to promote cell proliferation and protect TSPCs in TSPC therapy.

Funder

China Postdoctoral Science Foundation

Sichuan University

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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