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Temporal dynamic changes of connexin 43 expression in C6 cells following lipopolysaccharide stimulation☆

Connexin 43, a gap junction protein, is expressed mainly in glia in the central nervous system. Neuroinflammation plays an important role in central nervous system injury. Changes to glial connexin 43 levels and neuroinflammation may trigger brain injury and neurodegenerative diseases. To illustrate...

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Autores principales: Liu, Ling, Gao, Zhenping, Zhang, Linbo, Su, Lue, Dong, Guojun, Yu, Haiyang, Tian, Jiayi, Zhao, Hang, Xu, Yanyan, Liu, Haiyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298888/
https://www.ncbi.nlm.nih.gov/pubmed/25624823
http://dx.doi.org/10.3969/j.issn.1673-5374.2012.25.004
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author Liu, Ling
Gao, Zhenping
Zhang, Linbo
Su, Lue
Dong, Guojun
Yu, Haiyang
Tian, Jiayi
Zhao, Hang
Xu, Yanyan
Liu, Haiyan
author_facet Liu, Ling
Gao, Zhenping
Zhang, Linbo
Su, Lue
Dong, Guojun
Yu, Haiyang
Tian, Jiayi
Zhao, Hang
Xu, Yanyan
Liu, Haiyan
author_sort Liu, Ling
collection PubMed
description Connexin 43, a gap junction protein, is expressed mainly in glia in the central nervous system. Neuroinflammation plays an important role in central nervous system injury. Changes to glial connexin 43 levels and neuroinflammation may trigger brain injury and neurodegenerative diseases. To illustrate the relationship between connexin 43 and neuroinflammation, this study investigated how connexin 43 expression levels change in lipopolysaccharide-stimulated rat C6 glioma cells. C6 cells were treated with 0.05, 0.25, 0.5, 1, 2.5 and 5 μg/mL lipopolysaccharide for 24 hours. The nitrite estimation-detected nitric oxide release level was elevated substantially after lipopolysaccharide stimulation. To test the transcriptional level changes of inducible nitric oxide synthase, tumor necrosis factor-α and connexin 43 mRNA, C6 cells were treated with 5 μg/mL lipopolysaccharide for 3–48 hours. Reverse transcription-PCR showed that the expression of inducible nitric oxide synthase and tumor necrosis factor-α mRNA increased over time, but connexin 43 mRNA levels increased in lipopolysaccharide-stimulated C6 cells at 3 and 6 hours, and then decreased from 12 to 48 hours. Connexin 43 protein expression was detected by immunofluorescence staining, and the protein levels matched the mRNA expression levels. These results suggest that connexin 43 expression is biphasic in lipopolysaccharide-induced neuroinflammation in C6 cells, which may be correlated with the connexin 43 compensatory mechanism.
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spelling pubmed-42988882015-01-26 Temporal dynamic changes of connexin 43 expression in C6 cells following lipopolysaccharide stimulation☆ Liu, Ling Gao, Zhenping Zhang, Linbo Su, Lue Dong, Guojun Yu, Haiyang Tian, Jiayi Zhao, Hang Xu, Yanyan Liu, Haiyan Neural Regen Res Research and Report Article: Brain Injury and Neural Regeneration Connexin 43, a gap junction protein, is expressed mainly in glia in the central nervous system. Neuroinflammation plays an important role in central nervous system injury. Changes to glial connexin 43 levels and neuroinflammation may trigger brain injury and neurodegenerative diseases. To illustrate the relationship between connexin 43 and neuroinflammation, this study investigated how connexin 43 expression levels change in lipopolysaccharide-stimulated rat C6 glioma cells. C6 cells were treated with 0.05, 0.25, 0.5, 1, 2.5 and 5 μg/mL lipopolysaccharide for 24 hours. The nitrite estimation-detected nitric oxide release level was elevated substantially after lipopolysaccharide stimulation. To test the transcriptional level changes of inducible nitric oxide synthase, tumor necrosis factor-α and connexin 43 mRNA, C6 cells were treated with 5 μg/mL lipopolysaccharide for 3–48 hours. Reverse transcription-PCR showed that the expression of inducible nitric oxide synthase and tumor necrosis factor-α mRNA increased over time, but connexin 43 mRNA levels increased in lipopolysaccharide-stimulated C6 cells at 3 and 6 hours, and then decreased from 12 to 48 hours. Connexin 43 protein expression was detected by immunofluorescence staining, and the protein levels matched the mRNA expression levels. These results suggest that connexin 43 expression is biphasic in lipopolysaccharide-induced neuroinflammation in C6 cells, which may be correlated with the connexin 43 compensatory mechanism. Medknow Publications & Media Pvt Ltd 2012-09-05 /pmc/articles/PMC4298888/ /pubmed/25624823 http://dx.doi.org/10.3969/j.issn.1673-5374.2012.25.004 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research and Report Article: Brain Injury and Neural Regeneration
Liu, Ling
Gao, Zhenping
Zhang, Linbo
Su, Lue
Dong, Guojun
Yu, Haiyang
Tian, Jiayi
Zhao, Hang
Xu, Yanyan
Liu, Haiyan
Temporal dynamic changes of connexin 43 expression in C6 cells following lipopolysaccharide stimulation☆
title Temporal dynamic changes of connexin 43 expression in C6 cells following lipopolysaccharide stimulation☆
title_full Temporal dynamic changes of connexin 43 expression in C6 cells following lipopolysaccharide stimulation☆
title_fullStr Temporal dynamic changes of connexin 43 expression in C6 cells following lipopolysaccharide stimulation☆
title_full_unstemmed Temporal dynamic changes of connexin 43 expression in C6 cells following lipopolysaccharide stimulation☆
title_short Temporal dynamic changes of connexin 43 expression in C6 cells following lipopolysaccharide stimulation☆
title_sort temporal dynamic changes of connexin 43 expression in c6 cells following lipopolysaccharide stimulation☆
topic Research and Report Article: Brain Injury and Neural Regeneration
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298888/
https://www.ncbi.nlm.nih.gov/pubmed/25624823
http://dx.doi.org/10.3969/j.issn.1673-5374.2012.25.004
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