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Expression analysis on 14-3-3 proteins in regenerative liver following partial hepatectomy
Xue, Deming; Xue, Yang; Niu, Zhipeng; Guo, Xueqiang; Xu, Cunshuan.
Affiliation
  • Xue, Deming; Henan Normal University. College of Life Science. Xinxiang. CN
  • Xue, Yang; Henan Normal University. College of Life Science. Xinxiang. CN
  • Niu, Zhipeng; Henan Normal University. College of Life Science. Xinxiang. CN
  • Guo, Xueqiang; Henan Normal University. College of Life Science. Xinxiang. CN
  • Xu, Cunshuan; Henan Normal University. College of Life Science. Xinxiang. CN
Genet. mol. biol ; 40(4): 855-859, Oct.-Dec. 2017. graf
Article in English | LILACS | ID: biblio-892442
Responsible library: BR26.1
ABSTRACT
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.


Full text: Available Collection: International databases Database: LILACS Language: English Journal: Genet. mol. biol Journal subject: Genetics Year: 2017 Document type: Article / Project document Affiliation country: China Institution/Affiliation country: Henan Normal University/CN

Full text: Available Collection: International databases Database: LILACS Language: English Journal: Genet. mol. biol Journal subject: Genetics Year: 2017 Document type: Article / Project document Affiliation country: China Institution/Affiliation country: Henan Normal University/CN
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