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Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging

Knee cartilage is in an aqueous environment filled with synovial fluid consisting of water, various nutrients, and ions to maintain chondrocyte homeostasis. Aquaporins (AQPs) are water channel proteins that play an important role in water exchange in cells, and AQP1, -3, and -4 are known to be expre...

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Autores principales: Kyung, Bong Soo, Jung, Koo Whang, Yeo, Woo Jin, Seo, Hye Kyung, Lee, Yong-Soo, Suh, Dong Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516946/
https://www.ncbi.nlm.nih.gov/pubmed/34650163
http://dx.doi.org/10.1038/s41598-021-99885-7
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author Kyung, Bong Soo
Jung, Koo Whang
Yeo, Woo Jin
Seo, Hye Kyung
Lee, Yong-Soo
Suh, Dong Won
author_facet Kyung, Bong Soo
Jung, Koo Whang
Yeo, Woo Jin
Seo, Hye Kyung
Lee, Yong-Soo
Suh, Dong Won
author_sort Kyung, Bong Soo
collection PubMed
description Knee cartilage is in an aqueous environment filled with synovial fluid consisting of water, various nutrients, and ions to maintain chondrocyte homeostasis. Aquaporins (AQPs) are water channel proteins that play an important role in water exchange in cells, and AQP1, -3, and -4 are known to be expressed predominantly in cartilage. We evaluated the changes in AQP expression in chondrocytes from human knee articular cartilage in patients of different ages and identified the key factor(s) that mediate age-induced alteration in AQP expression. The mRNA and protein expression of AQP1, -3 and -4 were significantly decreased in fibrocartilage compared to hyaline cartilage and in articular cartilage from older osteoarthritis patients compared to that from young patients. Gene and protein expression of AQP1, -3 and -4 were altered during the chondrogenic differentiation of C3H10T1/2 cells. The causative factors for age-associated decrease in AQP included H(2)O(2), TNFα, and HMGB1 for AQP1, -3, and -4, respectively. In particular, the protective effect of AQP4 reduction following HMGB1 neutralization was noteworthy. The identification of other potent molecules that regulate AQP expression represents a promising therapeutic approach to suppress cartilage degeneration during aging.
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spelling pubmed-85169462021-10-15 Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging Kyung, Bong Soo Jung, Koo Whang Yeo, Woo Jin Seo, Hye Kyung Lee, Yong-Soo Suh, Dong Won Sci Rep Article Knee cartilage is in an aqueous environment filled with synovial fluid consisting of water, various nutrients, and ions to maintain chondrocyte homeostasis. Aquaporins (AQPs) are water channel proteins that play an important role in water exchange in cells, and AQP1, -3, and -4 are known to be expressed predominantly in cartilage. We evaluated the changes in AQP expression in chondrocytes from human knee articular cartilage in patients of different ages and identified the key factor(s) that mediate age-induced alteration in AQP expression. The mRNA and protein expression of AQP1, -3 and -4 were significantly decreased in fibrocartilage compared to hyaline cartilage and in articular cartilage from older osteoarthritis patients compared to that from young patients. Gene and protein expression of AQP1, -3 and -4 were altered during the chondrogenic differentiation of C3H10T1/2 cells. The causative factors for age-associated decrease in AQP included H(2)O(2), TNFα, and HMGB1 for AQP1, -3, and -4, respectively. In particular, the protective effect of AQP4 reduction following HMGB1 neutralization was noteworthy. The identification of other potent molecules that regulate AQP expression represents a promising therapeutic approach to suppress cartilage degeneration during aging. Nature Publishing Group UK 2021-10-14 /pmc/articles/PMC8516946/ /pubmed/34650163 http://dx.doi.org/10.1038/s41598-021-99885-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kyung, Bong Soo
Jung, Koo Whang
Yeo, Woo Jin
Seo, Hye Kyung
Lee, Yong-Soo
Suh, Dong Won
Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
title Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
title_full Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
title_fullStr Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
title_full_unstemmed Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
title_short Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
title_sort differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516946/
https://www.ncbi.nlm.nih.gov/pubmed/34650163
http://dx.doi.org/10.1038/s41598-021-99885-7
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