Effect of tetrahedral framework nucleic acids on the reconstruction of tendon‐to‐bone injuries after rotator cuff tears

Author:

Li Pinxue12,Fu Liwei12,Ning Chao1,Wu Jiang1,Xu Zizheng12,Liao Zhiyao12,Gao Cangjian1,Sui Xiang1,Lin Yunfeng3ORCID,Liu Shuyun1,Yuan Zhiguo4,Guo Quanyi12ORCID

Affiliation:

1. Institute of Orthopedics Chinese PLA General Hospital, the First Medical Center, Beijing Key Laboratory of Regenerative Medicine in Orthopedics, Key Laboratory of Musculoskeletal Trauma & War Injuries PLA Beijing People's Republic of China

2. School of Medicine Nankai University Tianjin People's Republic of China

3. State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology Sichuan University Chengdu People's Republic of China

4. Department of Bone and Joint Surgery, Renji Hospital School of Medicine, Shanghai Jiaotong University Shanghai People's Republic of China

Abstract

AbstractClinicians and researchers have always faced challenges in performing surgery for rotator cuff tears (RCT) due to the intricate nature of the tendon‐bone gradient and the limited long‐term effectiveness. At the same time, the occurrence of an inflammatory microenvironment further aggravates tissue damage, which has a negative impact on the regeneration process of mesenchymal stem cells (MSCs) and eventually leads to the production of scar tissue. Tetrahedral framework nucleic acids (tFNAs), novel nanomaterials, have shown great potential in biomedicine due to their strong biocompatibility, excellent cellular internalisation ability, and unparalleled programmability. The objective of this research was to examine if tFNAs have a positive effect on regeneration after RCTs. Experiments conducted in a controlled environment demonstrated that tFNAs hindered the assembly of inflammasomes in macrophages, resulting in a decrease in the release of inflammatory factors. Next, tFNAs were shown to exert a protective effect on the osteogenic and chondrogenic differentiation of bone marrow MSCs under inflammatory conditions. The in vitro results also demonstrated the regulatory effect of tFNAs on tendon‐related protein expression levels in tenocytes after inflammatory stimulation. Finally, intra‐articular injection of tFNAs into a rat RCT model showed that tFNAs improved tendon‐to‐bone healing, suggesting that tFNAs may be promising tendon‐to‐bone protective agents for the treatment of RCTs.

Publisher

Wiley

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