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  4. The effect of the repression of oxidative stress on tenocyte differentiation: A preliminary study of a rat cell model using a novel differential tensile strain bioreactor
 
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The effect of the repression of oxidative stress on tenocyte differentiation: A preliminary study of a rat cell model using a novel differential tensile strain bioreactor

Journal
International Journal of Molecular Sciences
Journal Volume
20
Journal Issue
14
Date Issued
2019-07-02
Author(s)
MING-YEN HSIAO  
Lin, Ping Cheng
Liao, Wei Hao
WEN-SHIANG CHEN  
Hsu, Chia Hsien
He, Cheng Kun
Wu, Ya Wen
Gefen, Amit
Iafisco, Michele
Liu, Lixin
FENG-HUEI LIN  
DOI
10.3390/ijms20143437
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/480858
URL
https://api.elsevier.com/content/abstract/scopus_id/85070473667
Abstract
© 2019 by the authors. Licensee MDPI, Basel, Switzerland. Because of limitations in the current understanding of the exact pathogenesis of tendinopathy, and the lack of an optimal experimental model, effective therapy for the disease is currently unavailable. This study aims to prove that repression of oxidative stress modulates the differentiation of tendon-derived cells (TDCs) sustaining excessive tensile strains, and proposes a novel bioreactor capable of applying differential tensile strains to cultured cells simultaneously. TDCs, including tendon-derived stem cells, tenoblasts, tenocytes, and fibroblasts, were isolated from the patellar tendons of Sprague-Dawley rats. Cyclic uniaxial stretching with 4% or 8% strain at 0.5 Hz for 8 h was applied to TDCs. TDCs subjected to 8% strain were treated with epigallocatechin gallate (EGCG), piracetam, or no medication. Genes representing non-tenocyte lineage (Pparg, Sox9, and Runx2) and type I and type III collagen were analyzed by quantitative polymerase chain reaction. The 8% strain group showed increased expression of non-tenocyte lineage genes and type III/type I collagen ratios compared with the control and 4% strain groups, and the increased expression was ameliorated with addition of EGCG and piracetam. The model developed in this work could be applied to future research on the pathophysiology of tendinopathy and development of treatment options for the disease. Repression of oxidative stress diminishes the expression of genes indicating aberrant differentiation in a rat cell model, which indicates potential therapeutic intervention of tendinopathy, the often relentlessly degenerate condition.
Subjects
Cell model | Oxidative stress | Tendinopathy
SDGs

[SDGs]SDG3

Publisher
MDPI
Type
journal article

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