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Histology and molecular pathology of iliotibial tract contracture in patients with gluteal muscle contracture

The present study aimed to examine the pathologic changes of the iliotibial tract and discusses its relationship with gluteal muscle contracture. Samples of contractual iliotibial tracts were collected from six patients with contractures of the gluteal muscles and iliotibial tracts during their surg...

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Autores principales: Yuan, Bang-tuo, Qu, Feng, Wang, Shao-xia, Qi, Wei, Shen, Xue-zhen, Li, Chun-bao, Liu, Yu-jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753321/
https://www.ncbi.nlm.nih.gov/pubmed/31467177
http://dx.doi.org/10.1042/BSR20181351
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author Yuan, Bang-tuo
Qu, Feng
Wang, Shao-xia
Qi, Wei
Shen, Xue-zhen
Li, Chun-bao
Liu, Yu-jie
author_facet Yuan, Bang-tuo
Qu, Feng
Wang, Shao-xia
Qi, Wei
Shen, Xue-zhen
Li, Chun-bao
Liu, Yu-jie
author_sort Yuan, Bang-tuo
collection PubMed
description The present study aimed to examine the pathologic changes of the iliotibial tract and discusses its relationship with gluteal muscle contracture. Samples of contractual iliotibial tracts were collected from six patients with contractures of the gluteal muscles and iliotibial tracts during their surgical treatment. Samples of normal iliotibial tracts were collected from six patients receiving surgeries for avascular necrosis of the femoral head who had no contractures of the gluteal muscles and iliotibial tracts. The tissue samples were stained using Hematoxylin and Eosin (H&E), Masson’s trichrome, and Sirius Red. The mRNA and protein levels of various tissue repair genes were determined using quantitative real-time PCR and Western blotting. Both the normal and contractual iliotibial tracts consisted of type I and III collagens. The contractual iliotibial tracts had a significantly higher proportion of type III collagen in comparison with the normal iliotibial tracts. The mRNA expression levels and protein levels of tissue repair genes TGFβ 1, bFGF, and matrix metalloproteinase-1 (MMP-1) in the contractual iliotibial tracts were up-regulated in comparison with that in the normal iliotibial tracts. However, the mRNA expression levels and protein levels of tissue inhibitors of metalloproteinase-1 (TIMP) in the contractual iliotibial tracts were down-regulated in comparison with that in the normal iliotibial tracts. The contractures of both the gluteal muscles and the iliotibial tracts share similar histology and molecular pathology. Our results indicate that iliotibial tract contracture is secondary to the gluteal muscle contracture and is a constant tissue repair process.
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spelling pubmed-67533212019-09-25 Histology and molecular pathology of iliotibial tract contracture in patients with gluteal muscle contracture Yuan, Bang-tuo Qu, Feng Wang, Shao-xia Qi, Wei Shen, Xue-zhen Li, Chun-bao Liu, Yu-jie Biosci Rep Research Articles The present study aimed to examine the pathologic changes of the iliotibial tract and discusses its relationship with gluteal muscle contracture. Samples of contractual iliotibial tracts were collected from six patients with contractures of the gluteal muscles and iliotibial tracts during their surgical treatment. Samples of normal iliotibial tracts were collected from six patients receiving surgeries for avascular necrosis of the femoral head who had no contractures of the gluteal muscles and iliotibial tracts. The tissue samples were stained using Hematoxylin and Eosin (H&E), Masson’s trichrome, and Sirius Red. The mRNA and protein levels of various tissue repair genes were determined using quantitative real-time PCR and Western blotting. Both the normal and contractual iliotibial tracts consisted of type I and III collagens. The contractual iliotibial tracts had a significantly higher proportion of type III collagen in comparison with the normal iliotibial tracts. The mRNA expression levels and protein levels of tissue repair genes TGFβ 1, bFGF, and matrix metalloproteinase-1 (MMP-1) in the contractual iliotibial tracts were up-regulated in comparison with that in the normal iliotibial tracts. However, the mRNA expression levels and protein levels of tissue inhibitors of metalloproteinase-1 (TIMP) in the contractual iliotibial tracts were down-regulated in comparison with that in the normal iliotibial tracts. The contractures of both the gluteal muscles and the iliotibial tracts share similar histology and molecular pathology. Our results indicate that iliotibial tract contracture is secondary to the gluteal muscle contracture and is a constant tissue repair process. Portland Press Ltd. 2019-09-20 /pmc/articles/PMC6753321/ /pubmed/31467177 http://dx.doi.org/10.1042/BSR20181351 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Yuan, Bang-tuo
Qu, Feng
Wang, Shao-xia
Qi, Wei
Shen, Xue-zhen
Li, Chun-bao
Liu, Yu-jie
Histology and molecular pathology of iliotibial tract contracture in patients with gluteal muscle contracture
title Histology and molecular pathology of iliotibial tract contracture in patients with gluteal muscle contracture
title_full Histology and molecular pathology of iliotibial tract contracture in patients with gluteal muscle contracture
title_fullStr Histology and molecular pathology of iliotibial tract contracture in patients with gluteal muscle contracture
title_full_unstemmed Histology and molecular pathology of iliotibial tract contracture in patients with gluteal muscle contracture
title_short Histology and molecular pathology of iliotibial tract contracture in patients with gluteal muscle contracture
title_sort histology and molecular pathology of iliotibial tract contracture in patients with gluteal muscle contracture
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6753321/
https://www.ncbi.nlm.nih.gov/pubmed/31467177
http://dx.doi.org/10.1042/BSR20181351
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