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Periostin in Mature Stage Localized Scleroderma

BACKGROUND: Periostin is a novel matricellular protein expressed in many tissues, including bone, periodontal ligament, and skin. Although its expression is prominent in various fibrotic conditions, studies of periostin in localized scleroderma are rare. OBJECTIVE: To investigate the expression of p...

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Autores principales: Kim, Min-Woo, Park, Jung Tae, Kim, Jung Ho, Koh, Seong-Joon, Yoon, Hyun-Sun, Cho, Soyun, Park, Hyun-sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438931/
https://www.ncbi.nlm.nih.gov/pubmed/28566901
http://dx.doi.org/10.5021/ad.2017.29.3.268
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author Kim, Min-Woo
Park, Jung Tae
Kim, Jung Ho
Koh, Seong-Joon
Yoon, Hyun-Sun
Cho, Soyun
Park, Hyun-sun
author_facet Kim, Min-Woo
Park, Jung Tae
Kim, Jung Ho
Koh, Seong-Joon
Yoon, Hyun-Sun
Cho, Soyun
Park, Hyun-sun
author_sort Kim, Min-Woo
collection PubMed
description BACKGROUND: Periostin is a novel matricellular protein expressed in many tissues, including bone, periodontal ligament, and skin. Although its expression is prominent in various fibrotic conditions, studies of periostin in localized scleroderma are rare. OBJECTIVE: To investigate the expression of periostin and other molecules in localized scleroderma. METHODS: A retrospective study of 14 patients with confirmed mature stage localized scleroderma was undertaken. Fourteen age-matched and biopsy site-matched subjects with normal skin were included as controls. Collagen fiber deposition, periostin, procollagen, transforming growth factor-β, and matrix metalloproteinase (MMP)-1 expression were assessed and compared between the two groups. Co-localization of α-smooth muscle actin and periostin was evaluated using confocal microscopy. RESULTS: Periostin was predominantly expressed along the dermo-epidermal junction in the controls. Conversely, patients with localized scleroderma demonstrated increased collagen fiber deposition and periostin expression that was more widely distributed along the entire dermis. MMP-1 staining showed increased expression in the epidermis and dermis of patients compared to scanty expression in the controls. A semi-quantitative evaluation showed a higher proportion of excessive collagen bundle deposition (57.1% vs. 7.1%, p=0.013), diffuse periostin positivity (42.9% vs. 0%, p=0.016), and moderate MMP-1 positivity (71.4% vs. 7.1%, p=0.001) in patients than in the controls. CONCLUSION: Compared to the controls, patients with localized scleroderma had enhanced periostin expression corresponding to increased collagen fiber deposition and unexpected overexpression of MMP-1. The results of this human in vivo study may implicate the pathogenesis of localized scleroderma.
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spelling pubmed-54389312017-06-01 Periostin in Mature Stage Localized Scleroderma Kim, Min-Woo Park, Jung Tae Kim, Jung Ho Koh, Seong-Joon Yoon, Hyun-Sun Cho, Soyun Park, Hyun-sun Ann Dermatol Original Article BACKGROUND: Periostin is a novel matricellular protein expressed in many tissues, including bone, periodontal ligament, and skin. Although its expression is prominent in various fibrotic conditions, studies of periostin in localized scleroderma are rare. OBJECTIVE: To investigate the expression of periostin and other molecules in localized scleroderma. METHODS: A retrospective study of 14 patients with confirmed mature stage localized scleroderma was undertaken. Fourteen age-matched and biopsy site-matched subjects with normal skin were included as controls. Collagen fiber deposition, periostin, procollagen, transforming growth factor-β, and matrix metalloproteinase (MMP)-1 expression were assessed and compared between the two groups. Co-localization of α-smooth muscle actin and periostin was evaluated using confocal microscopy. RESULTS: Periostin was predominantly expressed along the dermo-epidermal junction in the controls. Conversely, patients with localized scleroderma demonstrated increased collagen fiber deposition and periostin expression that was more widely distributed along the entire dermis. MMP-1 staining showed increased expression in the epidermis and dermis of patients compared to scanty expression in the controls. A semi-quantitative evaluation showed a higher proportion of excessive collagen bundle deposition (57.1% vs. 7.1%, p=0.013), diffuse periostin positivity (42.9% vs. 0%, p=0.016), and moderate MMP-1 positivity (71.4% vs. 7.1%, p=0.001) in patients than in the controls. CONCLUSION: Compared to the controls, patients with localized scleroderma had enhanced periostin expression corresponding to increased collagen fiber deposition and unexpected overexpression of MMP-1. The results of this human in vivo study may implicate the pathogenesis of localized scleroderma. The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2017-06 2017-05-11 /pmc/articles/PMC5438931/ /pubmed/28566901 http://dx.doi.org/10.5021/ad.2017.29.3.268 Text en Copyright © 2017 The Korean Dermatological Association and The Korean Society for Investigative Dermatology http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Min-Woo
Park, Jung Tae
Kim, Jung Ho
Koh, Seong-Joon
Yoon, Hyun-Sun
Cho, Soyun
Park, Hyun-sun
Periostin in Mature Stage Localized Scleroderma
title Periostin in Mature Stage Localized Scleroderma
title_full Periostin in Mature Stage Localized Scleroderma
title_fullStr Periostin in Mature Stage Localized Scleroderma
title_full_unstemmed Periostin in Mature Stage Localized Scleroderma
title_short Periostin in Mature Stage Localized Scleroderma
title_sort periostin in mature stage localized scleroderma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438931/
https://www.ncbi.nlm.nih.gov/pubmed/28566901
http://dx.doi.org/10.5021/ad.2017.29.3.268
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