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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...

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Autores principales: Zhu, Dandan, Song, Ke, Chen, Jinling, Wang, Jianxin, Sun, Xiaolei, Qian, Hongyan, Gu, Xijuan, Zhang, Lingbo, Qin, Yongwei, Duan, Yinong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
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.
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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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