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Interfacial Adipose Tissue in Systemic Sclerosis

PURPOSE OF REVIEW: This review provides a summary of recent insights into the role of the local white adipose tissue (WAT) in systemic sclerosis. RECENT FINDINGS: Adipocytes located in an interfacial WAT area adjacent to fibrotic lesions have an intermediate phenotype and special properties implicat...

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Autor principal: Kruglikov, Ilja L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5283508/
https://www.ncbi.nlm.nih.gov/pubmed/28138823
http://dx.doi.org/10.1007/s11926-017-0627-y
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author Kruglikov, Ilja L.
author_facet Kruglikov, Ilja L.
author_sort Kruglikov, Ilja L.
collection PubMed
description PURPOSE OF REVIEW: This review provides a summary of recent insights into the role of the local white adipose tissue (WAT) in systemic sclerosis. RECENT FINDINGS: Adipocytes located in an interfacial WAT area adjacent to fibrotic lesions have an intermediate phenotype and special properties implicated in fibrotic pathology in systemic sclerosis (SSc). The important role of these cells is recognized in different pathologies, such as wound healing, psoriasis, breast cancer, and prostate cancer. Additionally, both immature and mature adipocytes are involved in the appearance of fibroblast-like cells but exhibit different phenotypes and synthetic properties. SUMMARY: Adipocytes from interfacial WAT adjacent to the fibrotic area in SSc are phenotypically different from bulk adipocytes and are involved in pathogenesis of SSc. Immature and mature adipocytes from this WAT layer differentiate into various types of fibroblast-like cells, making the local ratio of immature to mature adipocytes in interfacial WAT of particular importance in SSc pathogenesis.
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spelling pubmed-52835082017-02-13 Interfacial Adipose Tissue in Systemic Sclerosis Kruglikov, Ilja L. Curr Rheumatol Rep Scleroderma (J Varga, Section Editor) PURPOSE OF REVIEW: This review provides a summary of recent insights into the role of the local white adipose tissue (WAT) in systemic sclerosis. RECENT FINDINGS: Adipocytes located in an interfacial WAT area adjacent to fibrotic lesions have an intermediate phenotype and special properties implicated in fibrotic pathology in systemic sclerosis (SSc). The important role of these cells is recognized in different pathologies, such as wound healing, psoriasis, breast cancer, and prostate cancer. Additionally, both immature and mature adipocytes are involved in the appearance of fibroblast-like cells but exhibit different phenotypes and synthetic properties. SUMMARY: Adipocytes from interfacial WAT adjacent to the fibrotic area in SSc are phenotypically different from bulk adipocytes and are involved in pathogenesis of SSc. Immature and mature adipocytes from this WAT layer differentiate into various types of fibroblast-like cells, making the local ratio of immature to mature adipocytes in interfacial WAT of particular importance in SSc pathogenesis. Springer US 2017-01-30 2017 /pmc/articles/PMC5283508/ /pubmed/28138823 http://dx.doi.org/10.1007/s11926-017-0627-y Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Scleroderma (J Varga, Section Editor)
Kruglikov, Ilja L.
Interfacial Adipose Tissue in Systemic Sclerosis
title Interfacial Adipose Tissue in Systemic Sclerosis
title_full Interfacial Adipose Tissue in Systemic Sclerosis
title_fullStr Interfacial Adipose Tissue in Systemic Sclerosis
title_full_unstemmed Interfacial Adipose Tissue in Systemic Sclerosis
title_short Interfacial Adipose Tissue in Systemic Sclerosis
title_sort interfacial adipose tissue in systemic sclerosis
topic Scleroderma (J Varga, Section Editor)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5283508/
https://www.ncbi.nlm.nih.gov/pubmed/28138823
http://dx.doi.org/10.1007/s11926-017-0627-y
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