Cargando…
Comparable response of ccn1 with ccn2 genes upon arthritis: An in vitro evaluation with a human chondrocytic cell line stimulated by a set of cytokines
BACKGROUND: The chondrosarcoma-derived HCS-2/8 has been known to be an excellent model of human articular chondrocytes. By mimicking the arthritic conditions through the treatment of HCS-2/8 cells with cytokines, we estimated the gene expression response of ccn1 and ccn2 during the course of joint i...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1112607/ https://www.ncbi.nlm.nih.gov/pubmed/15833111 http://dx.doi.org/10.1186/1478-811X-3-6 |
_version_ | 1782123941693751296 |
---|---|
author | Moritani, Norifumi H Kubota, Satoshi Sugahara, Toshio Takigawa, Masaharu |
author_facet | Moritani, Norifumi H Kubota, Satoshi Sugahara, Toshio Takigawa, Masaharu |
author_sort | Moritani, Norifumi H |
collection | PubMed |
description | BACKGROUND: The chondrosarcoma-derived HCS-2/8 has been known to be an excellent model of human articular chondrocytes. By mimicking the arthritic conditions through the treatment of HCS-2/8 cells with cytokines, we estimated the gene expression response of ccn1 and ccn2 during the course of joint inflammation in vitro. RESULTS: In order to mimic the initiation of inflammation, HCS-2/8 cells were treated with tumor necrosis factor (TNF)-α. To induce pro-inflammatory or reparative responses, TGF-β was employed. Effects of an anti-inflammatory glucocorticoid were also evaluated. After stimulation, expression levels of ccn1 and ccn2 were quantitatively analyzed. Surprisingly, not only ccn2, but also ccn1 expression was repressed upon TNF-α stimulation, whereas both mRNAs were uniformly induced by transforming growth factor (TGF)-β and a glucocorticoid. CONCLUSION: These results describing the same response during the course of inflammation suggest similar and co-operative roles of these 2 ccn family members in the course of arthritis. |
format | Text |
id | pubmed-1112607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-11126072005-05-14 Comparable response of ccn1 with ccn2 genes upon arthritis: An in vitro evaluation with a human chondrocytic cell line stimulated by a set of cytokines Moritani, Norifumi H Kubota, Satoshi Sugahara, Toshio Takigawa, Masaharu Cell Commun Signal Research BACKGROUND: The chondrosarcoma-derived HCS-2/8 has been known to be an excellent model of human articular chondrocytes. By mimicking the arthritic conditions through the treatment of HCS-2/8 cells with cytokines, we estimated the gene expression response of ccn1 and ccn2 during the course of joint inflammation in vitro. RESULTS: In order to mimic the initiation of inflammation, HCS-2/8 cells were treated with tumor necrosis factor (TNF)-α. To induce pro-inflammatory or reparative responses, TGF-β was employed. Effects of an anti-inflammatory glucocorticoid were also evaluated. After stimulation, expression levels of ccn1 and ccn2 were quantitatively analyzed. Surprisingly, not only ccn2, but also ccn1 expression was repressed upon TNF-α stimulation, whereas both mRNAs were uniformly induced by transforming growth factor (TGF)-β and a glucocorticoid. CONCLUSION: These results describing the same response during the course of inflammation suggest similar and co-operative roles of these 2 ccn family members in the course of arthritis. BioMed Central 2005-04-15 /pmc/articles/PMC1112607/ /pubmed/15833111 http://dx.doi.org/10.1186/1478-811X-3-6 Text en Copyright © 2005 Moritani et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Moritani, Norifumi H Kubota, Satoshi Sugahara, Toshio Takigawa, Masaharu Comparable response of ccn1 with ccn2 genes upon arthritis: An in vitro evaluation with a human chondrocytic cell line stimulated by a set of cytokines |
title | Comparable response of ccn1 with ccn2 genes upon arthritis: An in vitro evaluation with a human chondrocytic cell line stimulated by a set of cytokines |
title_full | Comparable response of ccn1 with ccn2 genes upon arthritis: An in vitro evaluation with a human chondrocytic cell line stimulated by a set of cytokines |
title_fullStr | Comparable response of ccn1 with ccn2 genes upon arthritis: An in vitro evaluation with a human chondrocytic cell line stimulated by a set of cytokines |
title_full_unstemmed | Comparable response of ccn1 with ccn2 genes upon arthritis: An in vitro evaluation with a human chondrocytic cell line stimulated by a set of cytokines |
title_short | Comparable response of ccn1 with ccn2 genes upon arthritis: An in vitro evaluation with a human chondrocytic cell line stimulated by a set of cytokines |
title_sort | comparable response of ccn1 with ccn2 genes upon arthritis: an in vitro evaluation with a human chondrocytic cell line stimulated by a set of cytokines |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1112607/ https://www.ncbi.nlm.nih.gov/pubmed/15833111 http://dx.doi.org/10.1186/1478-811X-3-6 |
work_keys_str_mv | AT moritaninorifumih comparableresponseofccn1withccn2genesuponarthritisaninvitroevaluationwithahumanchondrocyticcelllinestimulatedbyasetofcytokines AT kubotasatoshi comparableresponseofccn1withccn2genesuponarthritisaninvitroevaluationwithahumanchondrocyticcelllinestimulatedbyasetofcytokines AT sugaharatoshio comparableresponseofccn1withccn2genesuponarthritisaninvitroevaluationwithahumanchondrocyticcelllinestimulatedbyasetofcytokines AT takigawamasaharu comparableresponseofccn1withccn2genesuponarthritisaninvitroevaluationwithahumanchondrocyticcelllinestimulatedbyasetofcytokines |