Cargando…

Aspirin inhibits adipogenesis of tendon stem cells and lipids accumulation in rat injury tendon through regulating PTEN/PI3K/AKT signalling

Tendon injury repairs are big challenges in sports medicine, and fatty infiltration after tendon injury is very common and hampers tendon injury healing process. Tendon stem cells (TSCs), as precursors of tendon cells, have shown promising effect on injury tendon repair for their tenogenesis and ten...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Yunjiao, He, Gang, Wang, Feng, Zhang, Chenke, Ge, Zilu, Zheng, Xiaolong, Deng, Honghao, Yuan, Chengsong, Zhou, Binghua, Tao, Xu, Zhang, Jiqiang, Tang, Kanglai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815914/
https://www.ncbi.nlm.nih.gov/pubmed/31557405
http://dx.doi.org/10.1111/jcmm.14622
_version_ 1783463284097155072
author Wang, Yunjiao
He, Gang
Wang, Feng
Zhang, Chenke
Ge, Zilu
Zheng, Xiaolong
Deng, Honghao
Yuan, Chengsong
Zhou, Binghua
Tao, Xu
Zhang, Jiqiang
Tang, Kanglai
author_facet Wang, Yunjiao
He, Gang
Wang, Feng
Zhang, Chenke
Ge, Zilu
Zheng, Xiaolong
Deng, Honghao
Yuan, Chengsong
Zhou, Binghua
Tao, Xu
Zhang, Jiqiang
Tang, Kanglai
author_sort Wang, Yunjiao
collection PubMed
description Tendon injury repairs are big challenges in sports medicine, and fatty infiltration after tendon injury is very common and hampers tendon injury healing process. Tendon stem cells (TSCs), as precursors of tendon cells, have shown promising effect on injury tendon repair for their tenogenesis and tendon extracellular matrix formation. Adipocytes and lipids accumulation is a landmark event in pathological process of tendon injury, and this may induce tendon rupture in clinical practice. Based on this, it is important to inhibit TSCs adipogenesis and lipids infiltration to restore structure and function of injury tendon. Aspirin, as the representative of non‐steroidal anti‐inflammatory drugs (NSAIDs), has been widely used in tendon injury for its anti‐inflammatory and analgesic actions, but effect of aspirin on TSCs adipogenesis and fatty infiltration is still unclear. Under adipogenesis conditions, TSCs were treated with concentration gradient of aspirin. Oil red O staining was performed to observe changes of lipids accumulation. Next, we used RNA sequencing to compare profile changes of gene expression between induction group and aspirin‐treated group. Then, we verified the effect of filtrated signalling on TSCs adipogenesis. At last, we established rat tendon injury model and compared changes of biomechanical properties after aspirin treatment. The results showed that aspirin decreased lipids accumulation in injury tendon and inhibited TSCs adipogenesis. RNA sequencing filtrated PTEN/PI3K/AKT signalling as our target. After adding the signalling activators of VO‐Ohpic and IGF‐1, inhibited adipogenesis of TSCs was reversed. Still, aspirin promoted maximum loading, ultimate stress and breaking elongation of injury tendon. In conclusion, by down‐regulating PTEN/PI3K/AKT signalling, aspirin inhibited adipogenesis of TSCs and fatty infiltration in injury tendon, promoted biomechanical properties and decreased rupture risk of injury tendon. All these provided new therapeutic potential and medicine evidence of aspirin in treating tendon injury and tendinopathy.
format Online
Article
Text
id pubmed-6815914
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-68159142019-11-01 Aspirin inhibits adipogenesis of tendon stem cells and lipids accumulation in rat injury tendon through regulating PTEN/PI3K/AKT signalling Wang, Yunjiao He, Gang Wang, Feng Zhang, Chenke Ge, Zilu Zheng, Xiaolong Deng, Honghao Yuan, Chengsong Zhou, Binghua Tao, Xu Zhang, Jiqiang Tang, Kanglai J Cell Mol Med Original Articles Tendon injury repairs are big challenges in sports medicine, and fatty infiltration after tendon injury is very common and hampers tendon injury healing process. Tendon stem cells (TSCs), as precursors of tendon cells, have shown promising effect on injury tendon repair for their tenogenesis and tendon extracellular matrix formation. Adipocytes and lipids accumulation is a landmark event in pathological process of tendon injury, and this may induce tendon rupture in clinical practice. Based on this, it is important to inhibit TSCs adipogenesis and lipids infiltration to restore structure and function of injury tendon. Aspirin, as the representative of non‐steroidal anti‐inflammatory drugs (NSAIDs), has been widely used in tendon injury for its anti‐inflammatory and analgesic actions, but effect of aspirin on TSCs adipogenesis and fatty infiltration is still unclear. Under adipogenesis conditions, TSCs were treated with concentration gradient of aspirin. Oil red O staining was performed to observe changes of lipids accumulation. Next, we used RNA sequencing to compare profile changes of gene expression between induction group and aspirin‐treated group. Then, we verified the effect of filtrated signalling on TSCs adipogenesis. At last, we established rat tendon injury model and compared changes of biomechanical properties after aspirin treatment. The results showed that aspirin decreased lipids accumulation in injury tendon and inhibited TSCs adipogenesis. RNA sequencing filtrated PTEN/PI3K/AKT signalling as our target. After adding the signalling activators of VO‐Ohpic and IGF‐1, inhibited adipogenesis of TSCs was reversed. Still, aspirin promoted maximum loading, ultimate stress and breaking elongation of injury tendon. In conclusion, by down‐regulating PTEN/PI3K/AKT signalling, aspirin inhibited adipogenesis of TSCs and fatty infiltration in injury tendon, promoted biomechanical properties and decreased rupture risk of injury tendon. All these provided new therapeutic potential and medicine evidence of aspirin in treating tendon injury and tendinopathy. John Wiley and Sons Inc. 2019-09-26 2019-11 /pmc/articles/PMC6815914/ /pubmed/31557405 http://dx.doi.org/10.1111/jcmm.14622 Text en © 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Wang, Yunjiao
He, Gang
Wang, Feng
Zhang, Chenke
Ge, Zilu
Zheng, Xiaolong
Deng, Honghao
Yuan, Chengsong
Zhou, Binghua
Tao, Xu
Zhang, Jiqiang
Tang, Kanglai
Aspirin inhibits adipogenesis of tendon stem cells and lipids accumulation in rat injury tendon through regulating PTEN/PI3K/AKT signalling
title Aspirin inhibits adipogenesis of tendon stem cells and lipids accumulation in rat injury tendon through regulating PTEN/PI3K/AKT signalling
title_full Aspirin inhibits adipogenesis of tendon stem cells and lipids accumulation in rat injury tendon through regulating PTEN/PI3K/AKT signalling
title_fullStr Aspirin inhibits adipogenesis of tendon stem cells and lipids accumulation in rat injury tendon through regulating PTEN/PI3K/AKT signalling
title_full_unstemmed Aspirin inhibits adipogenesis of tendon stem cells and lipids accumulation in rat injury tendon through regulating PTEN/PI3K/AKT signalling
title_short Aspirin inhibits adipogenesis of tendon stem cells and lipids accumulation in rat injury tendon through regulating PTEN/PI3K/AKT signalling
title_sort aspirin inhibits adipogenesis of tendon stem cells and lipids accumulation in rat injury tendon through regulating pten/pi3k/akt signalling
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815914/
https://www.ncbi.nlm.nih.gov/pubmed/31557405
http://dx.doi.org/10.1111/jcmm.14622
work_keys_str_mv AT wangyunjiao aspirininhibitsadipogenesisoftendonstemcellsandlipidsaccumulationinratinjurytendonthroughregulatingptenpi3kaktsignalling
AT hegang aspirininhibitsadipogenesisoftendonstemcellsandlipidsaccumulationinratinjurytendonthroughregulatingptenpi3kaktsignalling
AT wangfeng aspirininhibitsadipogenesisoftendonstemcellsandlipidsaccumulationinratinjurytendonthroughregulatingptenpi3kaktsignalling
AT zhangchenke aspirininhibitsadipogenesisoftendonstemcellsandlipidsaccumulationinratinjurytendonthroughregulatingptenpi3kaktsignalling
AT gezilu aspirininhibitsadipogenesisoftendonstemcellsandlipidsaccumulationinratinjurytendonthroughregulatingptenpi3kaktsignalling
AT zhengxiaolong aspirininhibitsadipogenesisoftendonstemcellsandlipidsaccumulationinratinjurytendonthroughregulatingptenpi3kaktsignalling
AT denghonghao aspirininhibitsadipogenesisoftendonstemcellsandlipidsaccumulationinratinjurytendonthroughregulatingptenpi3kaktsignalling
AT yuanchengsong aspirininhibitsadipogenesisoftendonstemcellsandlipidsaccumulationinratinjurytendonthroughregulatingptenpi3kaktsignalling
AT zhoubinghua aspirininhibitsadipogenesisoftendonstemcellsandlipidsaccumulationinratinjurytendonthroughregulatingptenpi3kaktsignalling
AT taoxu aspirininhibitsadipogenesisoftendonstemcellsandlipidsaccumulationinratinjurytendonthroughregulatingptenpi3kaktsignalling
AT zhangjiqiang aspirininhibitsadipogenesisoftendonstemcellsandlipidsaccumulationinratinjurytendonthroughregulatingptenpi3kaktsignalling
AT tangkanglai aspirininhibitsadipogenesisoftendonstemcellsandlipidsaccumulationinratinjurytendonthroughregulatingptenpi3kaktsignalling