Overexpression of 14-3-3ζ Increases Brain Levels of C/EBP Homologous Protein CHOP

被引:4
作者
Brennan, Gary P. [1 ,2 ]
Jimenez-Mateos, Eva M. [1 ]
Sanz-Rodriguez, Amaya [1 ]
Mooney, Claire M. [1 ]
Tzivion, Guri [3 ]
Henshall, David C. [1 ]
Engel, Tobias [1 ]
机构
[1] Royal Coll Surgeons Ireland, Dept Physiol & Med Phys, Dublin 2, Ireland
[2] Univ Calif Irvine, Dept Pediat, Irvine, CA 92717 USA
[3] Univ Mississippi, Med Ctr, Dept Biochem, Jackson, MS 39216 USA
基金
爱尔兰科学基金会;
关键词
Tyrosine 3-Monooxygenase/Tryptophan 5-Monooxygenase Activation Protein; Zeta (14-3-3 Zeta protein); Endoplasmatic reticulumstress; Chop; microRNA-185; Cell death; ENDOPLASMIC-RETICULUM STRESS; CELL-DEATH; LOCALIZATION; BINDING;
D O I
10.1007/s12031-015-0510-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent studies demonstrated that overexpression of the molecular chaperone 14-3-3 zeta protects the brain against endoplasmic reticulum (ER) stress and prolonged seizures. The 14-3-3 targets responsible for improved neuronal survival after seizures remain unknown. Here we explored the mechanism, finding that protein levels of the ER-stress-associated transcription factor C/EBP homologous protein (CHOP) were significantly higher in 14-3-3 zeta-overexpressing mice. Since previous studies by us demonstrated that loss of CHOP increased vulnerability to seizure damage, we explored whether elevated CHOP levels result from 14-3-3 zeta overexpression and contribute to the protection. Pull-down experiments suggested that 14-3-3 zeta could bind CHOP as well as sequester a CHOP-targeting microRNA. However, 14-3-3 zeta overexpression remained protective against seizure-induced hippocampal injury in mice lacking CHOP. These studies reveal a novel function for 14-3-3 zeta in regulating CHOP levels but show that this is not required for protection against seizure-induced neuronal death.
引用
收藏
页码:255 / 262
页数:8
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