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REVIEW article

Front. Bioeng. Biotechnol.
Sec. Tissue Engineering and Regenerative Medicine
Volume 12 - 2024 | doi: 10.3389/fbioe.2024.1379773

Reprogramming Tendon Healing: A Guide to Novel Molecular Tools Provisionally Accepted

 Carlos J. Peniche Silva1 Elizabeth Rosado Balmayor2  Martijn van Griensven3*
  • 1Cell Biology Inspired Tissue Engineering, Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Netherlands
  • 2Experimental Orthopaedics and Trauma Surgery, Dept. of Orthopaedic, Trauma and Reconstructive Surgery, University Hospital RWTH Aachen, Germany
  • 3Trauma Surgery, Cell Biology Inspired Tissue Engineering, Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Netherlands

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Tendons are a frequent site of injury, which greatly impairs the movement and locomotion of patients. Regrettably, injuries at the tendon frequently require surgical intervention, which leads to a long path to recovery. Moreover, the healing of tendons often involves the formation of scar tissue at the site of injury with poor mechanical properties and prone to re-injury. Tissue engineering carries the promise of better and more effective solutions to the improper healing of tendons. Lately, the field of regenerative medicine has seen a significant increase in the focus on the potential use of noncoding RNAs (e.g. siRNAs, miRNAs, and lncRNAs) as molecular tools for tendon tissue engineering. This class of molecules is being investigated due to their ability to act as epigenetic regulators of gene expression and protein production. Thus, providing a molecular instrument to finetune, reprogram, and modulate the processes of tendon differentiation, healing, and regeneration. This review focuses particularly on the latest advances involving the use of siRNAs, miRNAs, and lncRNAs in tendon tissue engineering applications.

Keywords: Tendon, siRNA, miRNA, lncRNA, RNAi, mRNA silencing 1

Received: 31 Jan 2024; Accepted: 15 Apr 2024.

Copyright: © 2024 Peniche Silva, Rosado Balmayor and van Griensven. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Prof. Martijn van Griensven, Cell Biology Inspired Tissue Engineering, Institute for Technology-Inspired Regenerative Medicine, Maastricht University, Trauma Surgery, Maastricht, 81675, Bavaria, Netherlands