Cargando…

Effects of chondrocyte-derived extracellular matrix in a dry eye mouse model

PURPOSE: The occurrence of repetitive dry eye is accompanied by inflammation. This study investigated the anti-inflammatory effects of chondrocyte-derived extracellular matrix (CDECM) on the cornea and conjunctiva in a dry eye mouse model. METHODS: Dry eyes were experimentally induced in 12- to 16-w...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Chae Eun, Oh, Ha Na, Lee, Ji Hyun, Yang, Jae Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626784/
https://www.ncbi.nlm.nih.gov/pubmed/26604661
_version_ 1782398162629033984
author Kim, Chae Eun
Oh, Ha Na
Lee, Ji Hyun
Yang, Jae Wook
author_facet Kim, Chae Eun
Oh, Ha Na
Lee, Ji Hyun
Yang, Jae Wook
author_sort Kim, Chae Eun
collection PubMed
description PURPOSE: The occurrence of repetitive dry eye is accompanied by inflammation. This study investigated the anti-inflammatory effects of chondrocyte-derived extracellular matrix (CDECM) on the cornea and conjunctiva in a dry eye mouse model. METHODS: Dry eyes were experimentally induced in 12- to 16-week-old NOD.B10.H2(b) mice (Control) via subcutaneous injections of scopolamine (muscarinic receptor blocker) and exposure to an air draft for 10 days (desiccation stress [DS] 10D group). Tear volume and corneal smoothness were measured at 3, 5, 7, and 10 days after the instillation of PBS (PBS group) or CDECM (CDECM group). The corneas and conjunctivas were sectioned and stained with hematoxylin and eosin (H&E) and periodic acid Schiff (PAS). The expression of inflammatory markers (i.e., tumor necrosis factor-α [TNF-α], matrix metalloproteinase-2 [MMP-2], MMP-9, intercellular adhesion molecule-1 [ICAM-1], and vascular cell adhesion molecule-1 [VCAM-1]) was detected by quantitative real-time (qRT)-PCR and western blotting. All data were statistically processed using SPSS version 18.0. RESULTS: The instillation of CDECM after the removal of the DS increased tear production by up to 3.0-fold, and corneal smoothness improved to 80% compared to the PBS group (p<0.05). In the CDECM group, the detachment of the corneal epithelial cells was reduced by 73.3% compared to the PBS group, and the conjunctival goblet cell density was significantly recovered to the control levels (p<0.05). The expression of inflammatory factors was decreased in the cornea and conjunctiva of the CDECM group compared to the PBS group. CONCLUSIONS: These observations suggest that CDECM induced effective anti-inflammatory improvements in the cornea and conjunctiva in this experimental model of dry eye.
format Online
Article
Text
id pubmed-4626784
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Molecular Vision
record_format MEDLINE/PubMed
spelling pubmed-46267842015-11-24 Effects of chondrocyte-derived extracellular matrix in a dry eye mouse model Kim, Chae Eun Oh, Ha Na Lee, Ji Hyun Yang, Jae Wook Mol Vis Research Article PURPOSE: The occurrence of repetitive dry eye is accompanied by inflammation. This study investigated the anti-inflammatory effects of chondrocyte-derived extracellular matrix (CDECM) on the cornea and conjunctiva in a dry eye mouse model. METHODS: Dry eyes were experimentally induced in 12- to 16-week-old NOD.B10.H2(b) mice (Control) via subcutaneous injections of scopolamine (muscarinic receptor blocker) and exposure to an air draft for 10 days (desiccation stress [DS] 10D group). Tear volume and corneal smoothness were measured at 3, 5, 7, and 10 days after the instillation of PBS (PBS group) or CDECM (CDECM group). The corneas and conjunctivas were sectioned and stained with hematoxylin and eosin (H&E) and periodic acid Schiff (PAS). The expression of inflammatory markers (i.e., tumor necrosis factor-α [TNF-α], matrix metalloproteinase-2 [MMP-2], MMP-9, intercellular adhesion molecule-1 [ICAM-1], and vascular cell adhesion molecule-1 [VCAM-1]) was detected by quantitative real-time (qRT)-PCR and western blotting. All data were statistically processed using SPSS version 18.0. RESULTS: The instillation of CDECM after the removal of the DS increased tear production by up to 3.0-fold, and corneal smoothness improved to 80% compared to the PBS group (p<0.05). In the CDECM group, the detachment of the corneal epithelial cells was reduced by 73.3% compared to the PBS group, and the conjunctival goblet cell density was significantly recovered to the control levels (p<0.05). The expression of inflammatory factors was decreased in the cornea and conjunctiva of the CDECM group compared to the PBS group. CONCLUSIONS: These observations suggest that CDECM induced effective anti-inflammatory improvements in the cornea and conjunctiva in this experimental model of dry eye. Molecular Vision 2015-10-26 /pmc/articles/PMC4626784/ /pubmed/26604661 Text en Copyright © 2015 Molecular Vision. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited, used for non-commercial purposes, and is not altered or transformed.
spellingShingle Research Article
Kim, Chae Eun
Oh, Ha Na
Lee, Ji Hyun
Yang, Jae Wook
Effects of chondrocyte-derived extracellular matrix in a dry eye mouse model
title Effects of chondrocyte-derived extracellular matrix in a dry eye mouse model
title_full Effects of chondrocyte-derived extracellular matrix in a dry eye mouse model
title_fullStr Effects of chondrocyte-derived extracellular matrix in a dry eye mouse model
title_full_unstemmed Effects of chondrocyte-derived extracellular matrix in a dry eye mouse model
title_short Effects of chondrocyte-derived extracellular matrix in a dry eye mouse model
title_sort effects of chondrocyte-derived extracellular matrix in a dry eye mouse model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4626784/
https://www.ncbi.nlm.nih.gov/pubmed/26604661
work_keys_str_mv AT kimchaeeun effectsofchondrocytederivedextracellularmatrixinadryeyemousemodel
AT ohhana effectsofchondrocytederivedextracellularmatrixinadryeyemousemodel
AT leejihyun effectsofchondrocytederivedextracellularmatrixinadryeyemousemodel
AT yangjaewook effectsofchondrocytederivedextracellularmatrixinadryeyemousemodel