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An overview of carbonic anhydrases and membrane channels of synoviocytes in inflamed joints

The highly aggressive fibroblast-like synoviocytes (FLSs) are inflammatory mediators involved in synovial joint destruction. Membrane channels and transporters are essential components of the cell migration apparatus and are involved in various cellular functions. Although evidence is emerging that...

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Autores principales: Ji, Min Jeong, Hong, Jeong Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6735303/
https://www.ncbi.nlm.nih.gov/pubmed/31480869
http://dx.doi.org/10.1080/14756366.2019.1659791
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author Ji, Min Jeong
Hong, Jeong Hee
author_facet Ji, Min Jeong
Hong, Jeong Hee
author_sort Ji, Min Jeong
collection PubMed
description The highly aggressive fibroblast-like synoviocytes (FLSs) are inflammatory mediators involved in synovial joint destruction. Membrane channels and transporters are essential components of the cell migration apparatus and are involved in various cellular functions. Although evidence is emerging that cell migration is a physiological/pathological process, the mechanism of highly dynamic synoviocytes linked to the membrane channels and carbonic anhydrases (CAs) in inflamed joints is only partially understood. In this review, topics covered will give a brief overview of CAs and the membrane channels of synoviocytes. We have also systematically focused on the role of FLS channels and transporters under various conditions, including rheumatoid arthritis (RA), to understand the pathophysiology of the migration of synoviocytes as inflammatory mediators in joints.
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spelling pubmed-67353032019-09-16 An overview of carbonic anhydrases and membrane channels of synoviocytes in inflamed joints Ji, Min Jeong Hong, Jeong Hee J Enzyme Inhib Med Chem Review Article The highly aggressive fibroblast-like synoviocytes (FLSs) are inflammatory mediators involved in synovial joint destruction. Membrane channels and transporters are essential components of the cell migration apparatus and are involved in various cellular functions. Although evidence is emerging that cell migration is a physiological/pathological process, the mechanism of highly dynamic synoviocytes linked to the membrane channels and carbonic anhydrases (CAs) in inflamed joints is only partially understood. In this review, topics covered will give a brief overview of CAs and the membrane channels of synoviocytes. We have also systematically focused on the role of FLS channels and transporters under various conditions, including rheumatoid arthritis (RA), to understand the pathophysiology of the migration of synoviocytes as inflammatory mediators in joints. Taylor & Francis 2019-09-03 /pmc/articles/PMC6735303/ /pubmed/31480869 http://dx.doi.org/10.1080/14756366.2019.1659791 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ji, Min Jeong
Hong, Jeong Hee
An overview of carbonic anhydrases and membrane channels of synoviocytes in inflamed joints
title An overview of carbonic anhydrases and membrane channels of synoviocytes in inflamed joints
title_full An overview of carbonic anhydrases and membrane channels of synoviocytes in inflamed joints
title_fullStr An overview of carbonic anhydrases and membrane channels of synoviocytes in inflamed joints
title_full_unstemmed An overview of carbonic anhydrases and membrane channels of synoviocytes in inflamed joints
title_short An overview of carbonic anhydrases and membrane channels of synoviocytes in inflamed joints
title_sort overview of carbonic anhydrases and membrane channels of synoviocytes in inflamed joints
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6735303/
https://www.ncbi.nlm.nih.gov/pubmed/31480869
http://dx.doi.org/10.1080/14756366.2019.1659791
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