Expression analysis on 14-3-3 proteins in regenerative liver following partial hepatectomy

Detalhes bibliográficos
Autor(a) principal: Xue,Deming
Data de Publicação: 2017
Outros Autores: Xue,Yang, Niu,Zhipeng, Guo,Xueqiang, Xu,Cunshuan
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Genetics and Molecular Biology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572017000500855
Resumo: Abstract 14-3-3 proteins play a vital part in the regulation of cell cycle and apoptosis as signaling integration points. During liver regeneration, the quiescent hepatocytes go through hypertrophy and proliferation to restore liver weight. Therefore, we speculated that 14-3-3 proteins regulate the progression of liver regeneration. In this study, we analyzed the expression patterns of 14-3-3 proteins during liver regeneration of rat to provide an insight into the regenerative mechanism using western blotting. Only four isoforms (γ, ε, σ and τ/θ) of the 14-3-3 proteins were expressed in regenerative liver after partial hepatectomy (PH). The dual effects, the significant down-regulation of 14-3-3ε and the significant up-regulation of 14-3-3τ/θ at 2 h after PH, might play particularly important roles in S-phase entry. The significant peaks of 14-3-3σ at 30 h and of ε and τ/θ at 24 h might be closely related not only to the G2/M transition but also to the size of hepatocytes. Possibly, the peak of 14-3-3ε expression seen at 168 h plays critical roles in the termination of liver regeneration by inhibiting cellular proliferation.
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spelling Expression analysis on 14-3-3 proteins in regenerative liver following partial hepatectomyliver regeneration14-3-3 proteinswestern blottingAbstract 14-3-3 proteins play a vital part in the regulation of cell cycle and apoptosis as signaling integration points. During liver regeneration, the quiescent hepatocytes go through hypertrophy and proliferation to restore liver weight. Therefore, we speculated that 14-3-3 proteins regulate the progression of liver regeneration. In this study, we analyzed the expression patterns of 14-3-3 proteins during liver regeneration of rat to provide an insight into the regenerative mechanism using western blotting. Only four isoforms (γ, ε, σ and τ/θ) of the 14-3-3 proteins were expressed in regenerative liver after partial hepatectomy (PH). The dual effects, the significant down-regulation of 14-3-3ε and the significant up-regulation of 14-3-3τ/θ at 2 h after PH, might play particularly important roles in S-phase entry. The significant peaks of 14-3-3σ at 30 h and of ε and τ/θ at 24 h might be closely related not only to the G2/M transition but also to the size of hepatocytes. Possibly, the peak of 14-3-3ε expression seen at 168 h plays critical roles in the termination of liver regeneration by inhibiting cellular proliferation.Sociedade Brasileira de Genética2017-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572017000500855Genetics and Molecular Biology v.40 n.4 2017reponame:Genetics and Molecular Biologyinstname:Sociedade Brasileira de Genética (SBG)instacron:SBG10.1590/1678-4685-gmb-2017-0029info:eu-repo/semantics/openAccessXue,DemingXue,YangNiu,ZhipengGuo,XueqiangXu,Cunshuaneng2017-11-21T00:00:00Zoai:scielo:S1415-47572017000500855Revistahttp://www.gmb.org.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||editor@gmb.org.br1678-46851415-4757opendoar:2017-11-21T00:00Genetics and Molecular Biology - Sociedade Brasileira de Genética (SBG)false
dc.title.none.fl_str_mv Expression analysis on 14-3-3 proteins in regenerative liver following partial hepatectomy
title Expression analysis on 14-3-3 proteins in regenerative liver following partial hepatectomy
spellingShingle Expression analysis on 14-3-3 proteins in regenerative liver following partial hepatectomy
Xue,Deming
liver regeneration
14-3-3 proteins
western blotting
title_short Expression analysis on 14-3-3 proteins in regenerative liver following partial hepatectomy
title_full Expression analysis on 14-3-3 proteins in regenerative liver following partial hepatectomy
title_fullStr Expression analysis on 14-3-3 proteins in regenerative liver following partial hepatectomy
title_full_unstemmed Expression analysis on 14-3-3 proteins in regenerative liver following partial hepatectomy
title_sort Expression analysis on 14-3-3 proteins in regenerative liver following partial hepatectomy
author Xue,Deming
author_facet Xue,Deming
Xue,Yang
Niu,Zhipeng
Guo,Xueqiang
Xu,Cunshuan
author_role author
author2 Xue,Yang
Niu,Zhipeng
Guo,Xueqiang
Xu,Cunshuan
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Xue,Deming
Xue,Yang
Niu,Zhipeng
Guo,Xueqiang
Xu,Cunshuan
dc.subject.por.fl_str_mv liver regeneration
14-3-3 proteins
western blotting
topic liver regeneration
14-3-3 proteins
western blotting
description Abstract 14-3-3 proteins play a vital part in the regulation of cell cycle and apoptosis as signaling integration points. During liver regeneration, the quiescent hepatocytes go through hypertrophy and proliferation to restore liver weight. Therefore, we speculated that 14-3-3 proteins regulate the progression of liver regeneration. In this study, we analyzed the expression patterns of 14-3-3 proteins during liver regeneration of rat to provide an insight into the regenerative mechanism using western blotting. Only four isoforms (γ, ε, σ and τ/θ) of the 14-3-3 proteins were expressed in regenerative liver after partial hepatectomy (PH). The dual effects, the significant down-regulation of 14-3-3ε and the significant up-regulation of 14-3-3τ/θ at 2 h after PH, might play particularly important roles in S-phase entry. The significant peaks of 14-3-3σ at 30 h and of ε and τ/θ at 24 h might be closely related not only to the G2/M transition but also to the size of hepatocytes. Possibly, the peak of 14-3-3ε expression seen at 168 h plays critical roles in the termination of liver regeneration by inhibiting cellular proliferation.
publishDate 2017
dc.date.none.fl_str_mv 2017-12-01
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dc.relation.none.fl_str_mv 10.1590/1678-4685-gmb-2017-0029
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Genética
publisher.none.fl_str_mv Sociedade Brasileira de Genética
dc.source.none.fl_str_mv Genetics and Molecular Biology v.40 n.4 2017
reponame:Genetics and Molecular Biology
instname:Sociedade Brasileira de Genética (SBG)
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