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Proteomic analysis reveals rotator cuff injury caused by oxidative stress

BACKGROUND AND AIMS: Rotator cuff tendinopathy is common and is related to pain and dysfunction. However, the pathological mechanism of rotator cuff injury and shoulder pain is unclear. Objective: to investigate the pathological mechanism of rotator cuff injury and shoulder pain, and screen out the...

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Autores principales: Yuan, Tao, Qian, Hong, Yu, Xin, Meng, Jia, Lai, Cheng-Teng, Jiang, Hui, Zhao, Jian-Ning, Bao, Ni-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7975570/
https://www.ncbi.nlm.nih.gov/pubmed/33796243
http://dx.doi.org/10.1177/2040622320987057
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author Yuan, Tao
Qian, Hong
Yu, Xin
Meng, Jia
Lai, Cheng-Teng
Jiang, Hui
Zhao, Jian-Ning
Bao, Ni-Rong
author_facet Yuan, Tao
Qian, Hong
Yu, Xin
Meng, Jia
Lai, Cheng-Teng
Jiang, Hui
Zhao, Jian-Ning
Bao, Ni-Rong
author_sort Yuan, Tao
collection PubMed
description BACKGROUND AND AIMS: Rotator cuff tendinopathy is common and is related to pain and dysfunction. However, the pathological mechanism of rotator cuff injury and shoulder pain is unclear. Objective: to investigate the pathological mechanism of rotator cuff injury and shoulder pain, and screen out the marker proteins related to rotator cuff injury by proteomics. METHODS: Subacromial synovium specimens were collected from patients undergoing shoulder arthroscopic surgery. The experimental group were patients with rotator cuff repair surgery, and the control group were patients with habitual dislocation of the shoulder joint. Pathological examination was performed, and then followed by non-labeled quantitative proteomic detection. Finally, from analysis of the biological information of the samples, specific proteins related to rotator cuff injury and shoulder pain were deduced by functional analysis of differential proteins. RESULTS: All the patients in experimental groups were representative. A large number of adipocytes and inflammatory cells were found in the pathological sections of the experimental group; the proteomics analysis screen identified 80 proteins with significant differences, and the analysis of protein function revealed that S100A11 (p = 0.011), PLIN4 (p = 0.017), HYOU1 (p = 0.002) and CLIC1 (p = 0.007) were closely related to oxidative stress and chronic inflammation. CONCLUSION: Rotator cuff injury is closely related to oxidative stress and chronic inflammatory response, and the results suggest that the expression of S100A11, PLIN4, HYOU1 and CLIC1 in the synovium of rotator cuff injury provides a new marker for the study of its pathological mechanism.
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spelling pubmed-79755702021-03-31 Proteomic analysis reveals rotator cuff injury caused by oxidative stress Yuan, Tao Qian, Hong Yu, Xin Meng, Jia Lai, Cheng-Teng Jiang, Hui Zhao, Jian-Ning Bao, Ni-Rong Ther Adv Chronic Dis Tendinopathy: from pathophysiology to treatment BACKGROUND AND AIMS: Rotator cuff tendinopathy is common and is related to pain and dysfunction. However, the pathological mechanism of rotator cuff injury and shoulder pain is unclear. Objective: to investigate the pathological mechanism of rotator cuff injury and shoulder pain, and screen out the marker proteins related to rotator cuff injury by proteomics. METHODS: Subacromial synovium specimens were collected from patients undergoing shoulder arthroscopic surgery. The experimental group were patients with rotator cuff repair surgery, and the control group were patients with habitual dislocation of the shoulder joint. Pathological examination was performed, and then followed by non-labeled quantitative proteomic detection. Finally, from analysis of the biological information of the samples, specific proteins related to rotator cuff injury and shoulder pain were deduced by functional analysis of differential proteins. RESULTS: All the patients in experimental groups were representative. A large number of adipocytes and inflammatory cells were found in the pathological sections of the experimental group; the proteomics analysis screen identified 80 proteins with significant differences, and the analysis of protein function revealed that S100A11 (p = 0.011), PLIN4 (p = 0.017), HYOU1 (p = 0.002) and CLIC1 (p = 0.007) were closely related to oxidative stress and chronic inflammation. CONCLUSION: Rotator cuff injury is closely related to oxidative stress and chronic inflammatory response, and the results suggest that the expression of S100A11, PLIN4, HYOU1 and CLIC1 in the synovium of rotator cuff injury provides a new marker for the study of its pathological mechanism. SAGE Publications 2021-03-17 /pmc/articles/PMC7975570/ /pubmed/33796243 http://dx.doi.org/10.1177/2040622320987057 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Tendinopathy: from pathophysiology to treatment
Yuan, Tao
Qian, Hong
Yu, Xin
Meng, Jia
Lai, Cheng-Teng
Jiang, Hui
Zhao, Jian-Ning
Bao, Ni-Rong
Proteomic analysis reveals rotator cuff injury caused by oxidative stress
title Proteomic analysis reveals rotator cuff injury caused by oxidative stress
title_full Proteomic analysis reveals rotator cuff injury caused by oxidative stress
title_fullStr Proteomic analysis reveals rotator cuff injury caused by oxidative stress
title_full_unstemmed Proteomic analysis reveals rotator cuff injury caused by oxidative stress
title_short Proteomic analysis reveals rotator cuff injury caused by oxidative stress
title_sort proteomic analysis reveals rotator cuff injury caused by oxidative stress
topic Tendinopathy: from pathophysiology to treatment
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7975570/
https://www.ncbi.nlm.nih.gov/pubmed/33796243
http://dx.doi.org/10.1177/2040622320987057
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