Role of Phosphorylated HDAC4 in Stroke-Induced Angiogenesis.

Acetylation or deacetylation of chromatin proteins and transcription factors is part of a complex signaling system that is involved in the control of neurological disorders. Recent studies have demonstrated that histone deacetylases (HDACs) exert protective effects in attenuating neuronal injury aft...

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Publicado en:BioMed Research International Vol. 2017; pp. 1 - 12
Autores principales: Liu, Juan, Zhou, Xiang, Li, Qing, Zhou, Shu-Min, Hu, Bin, Hu, Guo-Wen, Niu, Xin, Guo, Shang-Chun, Wang, Yang, Deng, Zhi-Feng
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell 1/3/2017
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 1/3/2017
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2017/2957538
        120537012
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        atl: Role of Phosphorylated HDAC4 in Stroke-Induced Angiogenesis.
      aug:
        au:
          Liu, Juan
          Zhou, Xiang
          Li, Qing
          Zhou, Shu-Min
          Hu, Bin
          Hu, Guo-Wen
          Niu, Xin
          Guo, Shang-Chun
          Wang, Yang
          Deng, Zhi-Feng
        affil: Department of Neurosurgery, Shanghai Jiao Tong University Affiliated Sixth People’s Hospital, Shanghai, China
      sug:
        subj:
          Histones Physiology
          Stroke Physiopathology
          Animal Studies
          Phosphorylation
          Neovascularization, Pathologic
          Intracellular Signaling Peptides and Proteins
          Endothelium
          Anoxia
          Vascular Endothelial Growth Factors
          Rats
          Cell Culture Techniques
          Polymerase Chain Reaction
          Fluorescent Antibody Technique
          Antibodies
          Blotting, Western
          Wound Care
          Descriptive Statistics
          T-Tests
          Analysis of Variance
          Data Analysis Software
          Cerebral Ischemia Physiopathology
          Gene Expression
          Funding Source
      ab: Acetylation or deacetylation of chromatin proteins and transcription factors is part of a complex signaling system that is involved in the control of neurological disorders. Recent studies have demonstrated that histone deacetylases (HDACs) exert protective effects in attenuating neuronal injury after ischemic insults. Class IIa HDAC4 is highly expressed in the brain, and neuronal activity depends on the nucleocytoplasmic shuttling of HDAC4. However, little is known about HDAC4 and its roles in ischemic stroke. In this study, we report that phosphorylation of HDAC4 was remarkably upregulated after stroke and blockade of HDAC4 phosphorylation with GÖ6976 repressed stroke-induced angiogenesis. Phosphorylation of HDAC4 was also increased in endothelial cells hypoxia model and suppression of HDAC4 phosphorylation inhibited the tube formation and migration of endothelial cells in vitro. Furthermore, in addition to the inhibition of angiogenesis, blockade of HDAC4 phosphorylation suppressed the expression of genes downstream of HIF-VEGF signaling in vitro and in vivo. These data indicate that phosphorylated HDAC4 may serve as an important regulator in stroke-induced angiogenesis. The protective mechanism of phosphorylated HDAC4 is associated with HIF-VEGF signaling, implicating a novel therapeutic target in stroke.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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