It was reported that substance P had beneficial effects in the healing of acute tendon injury. However, the relationship between substance P and degenerative tendinopathy development remains unclear. The purpose of this study was to determine the role of substance P in the pathogenesis of tendinopathy. Healthy and tendinopathy tendon were harvested from human and tenocytes were cultured individually. The expression levels of genes associated with tendinopathy were compared. Next, substance P was exogenously administered to the healthy tenocyte and the effect was evaluated. The results showed that tendinopathy tenocytes had higher levels of COL3A1, MMP1, COX2, SCX, ACTA2, and substance P gene expression compared to healthy tenocytes. Next, substance P treatment on the healthy tenocyte displayed similar changes to that of the tendinopathy tenocytes. These differences between the two groups were also determined by Western blot. Additionally, cells with substance P had the tendinopathy change morphologically although cellular proliferation was significantly higher compared to that of the control group. In conclusion, substance P enhanced cellular proliferation, but concomitantly increased immature collagen (type 3 collagen). Substance P plays a crucial role in tendinopathy development and could be a future therapeutic target for treatment.
The Implication of Substance P in the Development of Tendinopathy: A Case Control Study
Soo-Hong Han,Wonchul Choi,Jiyeon Song,Jaehee Kim,Seungyong Lee,Youngrak Choi,Seongeun Byun,T. Ahn,Heejung Ahn,Catherine Ding,Lloyd Baik,Spencer Ward,K. Ting,Soonchul Lee
Published 2017 in International Journal of Molecular Sciences
ABSTRACT
PUBLICATION RECORD
- Publication year
2017
- Venue
International Journal of Molecular Sciences
- Publication date
2017-06-01
- Fields of study
Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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