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Oxygen and pH-sensitivity of human osteoarthritic chondrocytes in 3-D alginate bead culture system
OBJECTIVE: To identify the effect of alterations in physical parameters such as oxygen and pH on processes associated with cellular redox balance in osteoarthritic chondrocytes. METHOD: Human osteoarthritic chondrocytes (HOAC) were isolated from total knee arthroplasty samples and cultured in 3-D al...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
W.B. Saunders For The Osteoarthritis Research Society
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807787/ https://www.ncbi.nlm.nih.gov/pubmed/23850530 http://dx.doi.org/10.1016/j.joca.2013.06.028 |
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author | Collins, J.A. Moots, R.J. Winstanley, R. Clegg, P.D. Milner, P.I. |
author_facet | Collins, J.A. Moots, R.J. Winstanley, R. Clegg, P.D. Milner, P.I. |
author_sort | Collins, J.A. |
collection | PubMed |
description | OBJECTIVE: To identify the effect of alterations in physical parameters such as oxygen and pH on processes associated with cellular redox balance in osteoarthritic chondrocytes. METHOD: Human osteoarthritic chondrocytes (HOAC) were isolated from total knee arthroplasty samples and cultured in 3-D alginate beads in four different oxygen tensions (<1%, 2%, 5% and 21% O(2)), at pH 7.2 and 6.2 and in the presence or absence of 10 ng/ml, interleukin-1β (IL-1β). Cell viability, media glycosaminoglycan (GAG) levels, media nitrate/nitrate levels, active matrix metalloproteinase (MMP)-13 and intracellular adenosine triphosphate (ATP(i)) were measured over a 96-h time course. Intracellular reactive oxygen species (ROS), mitochondrial membrane potential, intracellular pH and reduced/oxidised glutathione (GSH/GSSG) were additionally measured after 48-h incubation under these experimental conditions. RESULTS: Hypoxia (2% O(2)) and anoxia (<1% O(2)), acidosis (pH 6.2) and 10 ng/ml IL-1β reduced HOAC cell viability and increased GAG media levels. Acidosis and IL-1β increased nitrite/nitrate release, but increases were moderate at 2% O(2) and significantly reduced at <1% O(2). ATP(i) was significantly reduced following hypoxia and anoxia and acidosis. At 48 h cellular ROS levels were increased by acidosis and IL-1β but reduced in hypoxia and anoxia. Mitochondrial membrane potential was reduced in low oxygen, acidosis and IL-1β. Anoxia also resulted in intracellular acidosis. GSH/GSSG ratio was reduced in low oxygen conditions, acidosis and IL-1β. CONCLUSIONS: This study shows that oxygen and pH affect elements of the redox system in HOAC including cellular anti-oxidants, mitochondrial membrane potential and ROS levels. |
format | Online Article Text |
id | pubmed-3807787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | W.B. Saunders For The Osteoarthritis Research Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-38077872013-11-01 Oxygen and pH-sensitivity of human osteoarthritic chondrocytes in 3-D alginate bead culture system Collins, J.A. Moots, R.J. Winstanley, R. Clegg, P.D. Milner, P.I. Osteoarthritis Cartilage Article OBJECTIVE: To identify the effect of alterations in physical parameters such as oxygen and pH on processes associated with cellular redox balance in osteoarthritic chondrocytes. METHOD: Human osteoarthritic chondrocytes (HOAC) were isolated from total knee arthroplasty samples and cultured in 3-D alginate beads in four different oxygen tensions (<1%, 2%, 5% and 21% O(2)), at pH 7.2 and 6.2 and in the presence or absence of 10 ng/ml, interleukin-1β (IL-1β). Cell viability, media glycosaminoglycan (GAG) levels, media nitrate/nitrate levels, active matrix metalloproteinase (MMP)-13 and intracellular adenosine triphosphate (ATP(i)) were measured over a 96-h time course. Intracellular reactive oxygen species (ROS), mitochondrial membrane potential, intracellular pH and reduced/oxidised glutathione (GSH/GSSG) were additionally measured after 48-h incubation under these experimental conditions. RESULTS: Hypoxia (2% O(2)) and anoxia (<1% O(2)), acidosis (pH 6.2) and 10 ng/ml IL-1β reduced HOAC cell viability and increased GAG media levels. Acidosis and IL-1β increased nitrite/nitrate release, but increases were moderate at 2% O(2) and significantly reduced at <1% O(2). ATP(i) was significantly reduced following hypoxia and anoxia and acidosis. At 48 h cellular ROS levels were increased by acidosis and IL-1β but reduced in hypoxia and anoxia. Mitochondrial membrane potential was reduced in low oxygen, acidosis and IL-1β. Anoxia also resulted in intracellular acidosis. GSH/GSSG ratio was reduced in low oxygen conditions, acidosis and IL-1β. CONCLUSIONS: This study shows that oxygen and pH affect elements of the redox system in HOAC including cellular anti-oxidants, mitochondrial membrane potential and ROS levels. W.B. Saunders For The Osteoarthritis Research Society 2013-11 /pmc/articles/PMC3807787/ /pubmed/23850530 http://dx.doi.org/10.1016/j.joca.2013.06.028 Text en © 2013 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Collins, J.A. Moots, R.J. Winstanley, R. Clegg, P.D. Milner, P.I. Oxygen and pH-sensitivity of human osteoarthritic chondrocytes in 3-D alginate bead culture system |
title | Oxygen and pH-sensitivity of human osteoarthritic chondrocytes in 3-D alginate bead culture system |
title_full | Oxygen and pH-sensitivity of human osteoarthritic chondrocytes in 3-D alginate bead culture system |
title_fullStr | Oxygen and pH-sensitivity of human osteoarthritic chondrocytes in 3-D alginate bead culture system |
title_full_unstemmed | Oxygen and pH-sensitivity of human osteoarthritic chondrocytes in 3-D alginate bead culture system |
title_short | Oxygen and pH-sensitivity of human osteoarthritic chondrocytes in 3-D alginate bead culture system |
title_sort | oxygen and ph-sensitivity of human osteoarthritic chondrocytes in 3-d alginate bead culture system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3807787/ https://www.ncbi.nlm.nih.gov/pubmed/23850530 http://dx.doi.org/10.1016/j.joca.2013.06.028 |
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