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Tissue chondrification and ossification in keloids with primary report of five cases

Keloid is commonly regarded as a benign skin tumour. Some keloids clinically exhibit hard tissue texture similar to that of cartilage or bone. We hypothesized that the keloid pathological niche environment is likely to induce keloid MSCs towards chondrogenic or osteogenic differentiation and leads t...

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Autores principales: Li, Qiannan, Tu, Tian, Wu, Xiaoli, Wang, Wenbo, Gao, Zhen, Liu, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9615288/
https://www.ncbi.nlm.nih.gov/pubmed/35315582
http://dx.doi.org/10.1111/iwj.13792
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author Li, Qiannan
Tu, Tian
Wu, Xiaoli
Wang, Wenbo
Gao, Zhen
Liu, Wei
author_facet Li, Qiannan
Tu, Tian
Wu, Xiaoli
Wang, Wenbo
Gao, Zhen
Liu, Wei
author_sort Li, Qiannan
collection PubMed
description Keloid is commonly regarded as a benign skin tumour. Some keloids clinically exhibit hard tissue texture similar to that of cartilage or bone. We hypothesized that the keloid pathological niche environment is likely to induce keloid MSCs towards chondrogenic or osteogenic differentiation and leads to cartilage or bone‐like tissue formation. The differences in tissue ossification, histology, mechanical properties, abnormal extracellular matrices and chondrogenic/osteogenic gene expression among sclerous keloids (SKs), regular keloids (RKs) and normal skins (NKs) were carefully examined. The sporadic ossified islets existed in SK group whereas no ossified/chondrified islet was found in other groups by micro‐CT reconstruction. H&E, Masson trichrome and safranin O staining revealed lacuna‐like structures in SKs, which were featured as bone/cartilage histology. Immunohistochemical staining showed overproduction of osteoprotegerin, type I and III collagen in SK group but similar production level of aggrecan among three groups. The biomechanical analysis demonstrated the weakest compliance of SK tissues. In addition, SK fibroblasts exhibited a relatively slower proliferation rate but higher expression levels of osteogenic and chondrogenic genes among all three groups. These cell populations also showed the strongest potential for lineage transformation. In conclusion, we first reported the presence of ossified and chondrified matrices in some extremely hard keloids in the present study.
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spelling pubmed-96152882022-10-31 Tissue chondrification and ossification in keloids with primary report of five cases Li, Qiannan Tu, Tian Wu, Xiaoli Wang, Wenbo Gao, Zhen Liu, Wei Int Wound J Original Articles Keloid is commonly regarded as a benign skin tumour. Some keloids clinically exhibit hard tissue texture similar to that of cartilage or bone. We hypothesized that the keloid pathological niche environment is likely to induce keloid MSCs towards chondrogenic or osteogenic differentiation and leads to cartilage or bone‐like tissue formation. The differences in tissue ossification, histology, mechanical properties, abnormal extracellular matrices and chondrogenic/osteogenic gene expression among sclerous keloids (SKs), regular keloids (RKs) and normal skins (NKs) were carefully examined. The sporadic ossified islets existed in SK group whereas no ossified/chondrified islet was found in other groups by micro‐CT reconstruction. H&E, Masson trichrome and safranin O staining revealed lacuna‐like structures in SKs, which were featured as bone/cartilage histology. Immunohistochemical staining showed overproduction of osteoprotegerin, type I and III collagen in SK group but similar production level of aggrecan among three groups. The biomechanical analysis demonstrated the weakest compliance of SK tissues. In addition, SK fibroblasts exhibited a relatively slower proliferation rate but higher expression levels of osteogenic and chondrogenic genes among all three groups. These cell populations also showed the strongest potential for lineage transformation. In conclusion, we first reported the presence of ossified and chondrified matrices in some extremely hard keloids in the present study. Blackwell Publishing Ltd 2022-03-21 /pmc/articles/PMC9615288/ /pubmed/35315582 http://dx.doi.org/10.1111/iwj.13792 Text en © 2022 Shanghai Tissue Engineering Key Laboratory. International Wound Journal published by Medicalhelplines.com Inc (3M) and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Li, Qiannan
Tu, Tian
Wu, Xiaoli
Wang, Wenbo
Gao, Zhen
Liu, Wei
Tissue chondrification and ossification in keloids with primary report of five cases
title Tissue chondrification and ossification in keloids with primary report of five cases
title_full Tissue chondrification and ossification in keloids with primary report of five cases
title_fullStr Tissue chondrification and ossification in keloids with primary report of five cases
title_full_unstemmed Tissue chondrification and ossification in keloids with primary report of five cases
title_short Tissue chondrification and ossification in keloids with primary report of five cases
title_sort tissue chondrification and ossification in keloids with primary report of five cases
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9615288/
https://www.ncbi.nlm.nih.gov/pubmed/35315582
http://dx.doi.org/10.1111/iwj.13792
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