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Updated: Jan 27, 2026

Applying a Three-dimensional Uniaxial Mechanical Stimulation Bioreactor System to Induce Tenogenic Differentiation of Tendon-Derived Stem Cells
Published on: August 1, 2020
MiR-378a suppresses tenogenic differentiation and tendon repair by targeting at TGF-β2
Yang Liu1,2, Lu Feng1, Jia Xu1,3
1Department of Orthopaedics and Traumatology, Faculty of Medicine, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China.
Background:
Tendons are a crucial component of the musculoskeletal system and responsible for transmission forces derived from muscle to bone. Patients with tendon injuries are often observed with decreased collagen production and matrix degeneration, and healing of tendon injuries remains a challenge as a result of limited understanding of tendon biology. Recent studies highlight the contribution of miR-378a on the regulation gene expression during tendon differentiation.
Methods:
We examined the tendon microstructure and tendon repair with using miR-378a knock-in transgenic mice, and the tendon-derived stem cells were also isolated from transgenic mice to study their tenogenic differentiation ability. Meanwhile, the expression levels of tenogenic markers were also examined in mouse tendon-derived stem cells transfected with miR-378a mimics during tenogenic differentiation. With using online prediction software and luciferase reporter assay, the binding target of miR-378a was also studied.
Results:
Our results indicated miR-378a impairs tenogenic differentiation and tendon repair by inhibition collagen and extracellular matrix production both in vitro and in vivo. We also demonstrated that miR-378a exert its inhibitory role during tenogenic differentiation through binding at TGFβ2 by luciferase reporter assay and western blot.
Conclusions:
Our investigation suggests that miR-378a could be considered as a new potential biomarker for tendon injury diagnosis or drug target for a possible therapeutic approach in future clinical practice.
Insights
MicroRNA-378a (miR-378a) hinders tendon healing and stem cell differentiation by inhibiting collagen production. This finding suggests miR-378a as a potential biomarker or therapeutic target for tendon injuries.
Area of Science:
- Musculoskeletal biology
- Molecular biology
- Regenerative medicine
Background:
- Tendon injuries involve decreased collagen and matrix degeneration, complicating healing.
- Understanding tendon biology is key to addressing healing challenges.
- MicroRNA-378a (miR-378a) is implicated in regulating gene expression during tendon differentiation.
Purpose of the Study:
- To investigate the role of miR-378a in tendon microstructure and repair.
- To assess the tenogenic differentiation potential of miR-378a-modified stem cells.
- To identify the molecular targets of miR-378a in tendon cells.
Main Methods:
- Utilized miR-378a knock-in transgenic mice to study tendon repair and microstructure.
- Isolated and cultured tendon-derived stem cells from transgenic mice.
- Employed miR-378a mimics, luciferase reporter assays, and western blot to analyze gene expression and binding targets.
Main Results:
- miR-378a was found to impair tenogenic differentiation and tendon repair both in vitro and in vivo.
- Inhibition of collagen and extracellular matrix production was observed due to miR-378a.
- miR-378a was confirmed to bind to TGFβ2, mediating its inhibitory effects.
Conclusions:
- miR-378a negatively regulates tendon stem cell differentiation and extracellular matrix production.
- TGFβ2 acts as a direct binding target of miR-378a in the context of tenogenesis.
- miR-378a presents potential as a biomarker for tendon injury diagnosis and a therapeutic target for tendon repair.
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