Cargando…

Osmolarity influences chondrocyte repair after injury in human articular cartilage

BACKGROUND: The purpose was to determine the influence of irrigation solution osmolarity on articular chondrocytes survival and metabolic state following mechanical injury. METHODS: Osteochondral explants were harvested from patients undergoing total knee arthroplasty for osteoarthritis and then cut...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Yuelong, Zhang, Yujun, Ding, Xiaoquan, Liu, Songyang, Sun, Tiezheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326434/
https://www.ncbi.nlm.nih.gov/pubmed/25626354
http://dx.doi.org/10.1186/s13018-015-0158-z
_version_ 1782356927608520704
author Huang, Yuelong
Zhang, Yujun
Ding, Xiaoquan
Liu, Songyang
Sun, Tiezheng
author_facet Huang, Yuelong
Zhang, Yujun
Ding, Xiaoquan
Liu, Songyang
Sun, Tiezheng
author_sort Huang, Yuelong
collection PubMed
description BACKGROUND: The purpose was to determine the influence of irrigation solution osmolarity on articular chondrocytes survival and metabolic state following mechanical injury. METHODS: Osteochondral explants were harvested from patients undergoing total knee arthroplasty for osteoarthritis and then cut through their full thickness to establish mechanical injury models. Cartilage explants were incubated in irrigation solutions (saline and balanced salt) with different osmolarities (180, 280, 380, 580 mOsm/L) for 2 h. The percentage of cell death (100 × number of dead cells/number of dead and live cells) was quantified with the laser confocal microscopy. The terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) assay was performed to detect apoptosis index of injured cartilage. The contents of proteoglycan elution were determined by spectrophotometer at 530 nm, and HIF-1α and type II collagen mRNA yields were quantified with real-time PCR. RESULTS: In situ dead chondrocytes were mainly localized to the superficial tangential region of injured cartilage edge after mechanical injury. The percentage of cell death was decreased, and proteoglycan elution was gradually reduced with the increasing of osmolarity. The apoptosis indices of TUNEL assay in different osmolarities had no significant difference (P = 0.158). HIF-1α and type II collagen mRNA yields were the least for chondrocytes exposed to 180 mOsm/L medium and were the greatest for chondrocytes exposed to 380 mOsm/L medium. Compared with the saline group, the cell death of superficial zone was significantly decreased (P = 0.001) and contents of proteoglycan elution were also significantly decreased (P = 0.045) in the balanced salt. HIF-1α (P = 0.017) and type II collagen (P = 0.034) mRNA yields in the chondrocytes exposed to the balanced salt were significantly more than the saline group. CONCLUSION: The osmolarity of irrigation solutions plays an important role in the survival and metabolic state of chondrocytes following mechanical injury, and the chondrocyte death is not caused by apoptosis. Increasing osmolarity of irrigation solutions may be chondroprotective with decreasing the chondrocyte death, reducing inhibition of metabolism and proteoglycan elution, ultimately preventing cartilage degeneration and promoting integrative repair.
format Online
Article
Text
id pubmed-4326434
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-43264342015-02-14 Osmolarity influences chondrocyte repair after injury in human articular cartilage Huang, Yuelong Zhang, Yujun Ding, Xiaoquan Liu, Songyang Sun, Tiezheng J Orthop Surg Res Research Article BACKGROUND: The purpose was to determine the influence of irrigation solution osmolarity on articular chondrocytes survival and metabolic state following mechanical injury. METHODS: Osteochondral explants were harvested from patients undergoing total knee arthroplasty for osteoarthritis and then cut through their full thickness to establish mechanical injury models. Cartilage explants were incubated in irrigation solutions (saline and balanced salt) with different osmolarities (180, 280, 380, 580 mOsm/L) for 2 h. The percentage of cell death (100 × number of dead cells/number of dead and live cells) was quantified with the laser confocal microscopy. The terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling (TUNEL) assay was performed to detect apoptosis index of injured cartilage. The contents of proteoglycan elution were determined by spectrophotometer at 530 nm, and HIF-1α and type II collagen mRNA yields were quantified with real-time PCR. RESULTS: In situ dead chondrocytes were mainly localized to the superficial tangential region of injured cartilage edge after mechanical injury. The percentage of cell death was decreased, and proteoglycan elution was gradually reduced with the increasing of osmolarity. The apoptosis indices of TUNEL assay in different osmolarities had no significant difference (P = 0.158). HIF-1α and type II collagen mRNA yields were the least for chondrocytes exposed to 180 mOsm/L medium and were the greatest for chondrocytes exposed to 380 mOsm/L medium. Compared with the saline group, the cell death of superficial zone was significantly decreased (P = 0.001) and contents of proteoglycan elution were also significantly decreased (P = 0.045) in the balanced salt. HIF-1α (P = 0.017) and type II collagen (P = 0.034) mRNA yields in the chondrocytes exposed to the balanced salt were significantly more than the saline group. CONCLUSION: The osmolarity of irrigation solutions plays an important role in the survival and metabolic state of chondrocytes following mechanical injury, and the chondrocyte death is not caused by apoptosis. Increasing osmolarity of irrigation solutions may be chondroprotective with decreasing the chondrocyte death, reducing inhibition of metabolism and proteoglycan elution, ultimately preventing cartilage degeneration and promoting integrative repair. BioMed Central 2015-01-28 /pmc/articles/PMC4326434/ /pubmed/25626354 http://dx.doi.org/10.1186/s13018-015-0158-z Text en © Huang et al.; licensee BioMed Central. 2015 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Huang, Yuelong
Zhang, Yujun
Ding, Xiaoquan
Liu, Songyang
Sun, Tiezheng
Osmolarity influences chondrocyte repair after injury in human articular cartilage
title Osmolarity influences chondrocyte repair after injury in human articular cartilage
title_full Osmolarity influences chondrocyte repair after injury in human articular cartilage
title_fullStr Osmolarity influences chondrocyte repair after injury in human articular cartilage
title_full_unstemmed Osmolarity influences chondrocyte repair after injury in human articular cartilage
title_short Osmolarity influences chondrocyte repair after injury in human articular cartilage
title_sort osmolarity influences chondrocyte repair after injury in human articular cartilage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326434/
https://www.ncbi.nlm.nih.gov/pubmed/25626354
http://dx.doi.org/10.1186/s13018-015-0158-z
work_keys_str_mv AT huangyuelong osmolarityinfluenceschondrocyterepairafterinjuryinhumanarticularcartilage
AT zhangyujun osmolarityinfluenceschondrocyterepairafterinjuryinhumanarticularcartilage
AT dingxiaoquan osmolarityinfluenceschondrocyterepairafterinjuryinhumanarticularcartilage
AT liusongyang osmolarityinfluenceschondrocyterepairafterinjuryinhumanarticularcartilage
AT suntiezheng osmolarityinfluenceschondrocyterepairafterinjuryinhumanarticularcartilage