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Expression of Septin4 in Schistosoma japonicum-infected mouse livers after praziquantel treatment
BACKGROUND: Septin4 (SEPT4) exists widely in human tissues and is related to mechanical stability, actin dynamics, membrane trafficking, viral replication and apoptosis. Data from many studies have suggested that SEPT4 plays a significant role in liver fibrosis. SEPT4 is down-regulated in the model...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298944/ https://www.ncbi.nlm.nih.gov/pubmed/25582427 http://dx.doi.org/10.1186/s13071-015-0640-9 |
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author | Zhu, Dandan Song, Ke Chen, Jinling Wang, Jianxin Sun, Xiaolei Qian, Hongyan Gu, Xijuan Zhang, Lingbo Qin, Yongwei Duan, Yinong |
author_facet | Zhu, Dandan Song, Ke Chen, Jinling Wang, Jianxin Sun, Xiaolei Qian, Hongyan Gu, Xijuan Zhang, Lingbo Qin, Yongwei Duan, Yinong |
author_sort | Zhu, Dandan |
collection | PubMed |
description | BACKGROUND: Septin4 (SEPT4) exists widely in human tissues and is related to mechanical stability, actin dynamics, membrane trafficking, viral replication and apoptosis. Data from many studies have suggested that SEPT4 plays a significant role in liver fibrosis. SEPT4 is down-regulated in the model of CCl(4) and BDL treated liver fibrosis. However, it is up-regulated and peaked at 12 weeks post-infection (p.i.), and then decreased subsequently in Schistosoma japonicum (S. japonicum) egg-induced liver fibrosis. The aim of this study was to observe the dynamic alteration of SEPT4 after the treatment of praziquantel (PZQ) in ICR mice infected with S. japonicum. METHODS: Expression of SEPT4 was determined by western blot, immunofluorescence and qRT-PCR. And pro-inflammatory cytokines IL-6 and TNF-α were detected by qRT-PCR. The number of eggs, the diameter of egg granulomas and fibrosis-associated genes were also measured. RESULTS: Our results showed that the granulomatous inflammation was reduced, whereafter the expression of SEPT4 on hepatic stellate cells (HSCs) was decreased after PZQ anti-schistosome therapy. And the variation tendency of SEPT4 had positive correlation with the inflammatory response in the area of S. japonicum egg granulomas. CONCLUSIONS: Based on these findings, the inhibition of the expression of the SEPT4 by PZQ might be due to alleviation of the inflammatory response at the chronic and advanced stage of S. japonicum infection. |
format | Online Article Text |
id | pubmed-4298944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42989442015-01-21 Expression of Septin4 in Schistosoma japonicum-infected mouse livers after praziquantel treatment Zhu, Dandan Song, Ke Chen, Jinling Wang, Jianxin Sun, Xiaolei Qian, Hongyan Gu, Xijuan Zhang, Lingbo Qin, Yongwei Duan, Yinong Parasit Vectors Research BACKGROUND: Septin4 (SEPT4) exists widely in human tissues and is related to mechanical stability, actin dynamics, membrane trafficking, viral replication and apoptosis. Data from many studies have suggested that SEPT4 plays a significant role in liver fibrosis. SEPT4 is down-regulated in the model of CCl(4) and BDL treated liver fibrosis. However, it is up-regulated and peaked at 12 weeks post-infection (p.i.), and then decreased subsequently in Schistosoma japonicum (S. japonicum) egg-induced liver fibrosis. The aim of this study was to observe the dynamic alteration of SEPT4 after the treatment of praziquantel (PZQ) in ICR mice infected with S. japonicum. METHODS: Expression of SEPT4 was determined by western blot, immunofluorescence and qRT-PCR. And pro-inflammatory cytokines IL-6 and TNF-α were detected by qRT-PCR. The number of eggs, the diameter of egg granulomas and fibrosis-associated genes were also measured. RESULTS: Our results showed that the granulomatous inflammation was reduced, whereafter the expression of SEPT4 on hepatic stellate cells (HSCs) was decreased after PZQ anti-schistosome therapy. And the variation tendency of SEPT4 had positive correlation with the inflammatory response in the area of S. japonicum egg granulomas. CONCLUSIONS: Based on these findings, the inhibition of the expression of the SEPT4 by PZQ might be due to alleviation of the inflammatory response at the chronic and advanced stage of S. japonicum infection. BioMed Central 2015-01-13 /pmc/articles/PMC4298944/ /pubmed/25582427 http://dx.doi.org/10.1186/s13071-015-0640-9 Text en © Zhu 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 Zhu, Dandan Song, Ke Chen, Jinling Wang, Jianxin Sun, Xiaolei Qian, Hongyan Gu, Xijuan Zhang, Lingbo Qin, Yongwei Duan, Yinong Expression of Septin4 in Schistosoma japonicum-infected mouse livers after praziquantel treatment |
title | Expression of Septin4 in Schistosoma japonicum-infected mouse livers after praziquantel treatment |
title_full | Expression of Septin4 in Schistosoma japonicum-infected mouse livers after praziquantel treatment |
title_fullStr | Expression of Septin4 in Schistosoma japonicum-infected mouse livers after praziquantel treatment |
title_full_unstemmed | Expression of Septin4 in Schistosoma japonicum-infected mouse livers after praziquantel treatment |
title_short | Expression of Septin4 in Schistosoma japonicum-infected mouse livers after praziquantel treatment |
title_sort | expression of septin4 in schistosoma japonicum-infected mouse livers after praziquantel treatment |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298944/ https://www.ncbi.nlm.nih.gov/pubmed/25582427 http://dx.doi.org/10.1186/s13071-015-0640-9 |
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