E4BP4 inhibits AngII-induced apoptosis in H9c2 cardiomyoblasts by activating the PI3K-Akt pathway and promoting calcium uptake

被引:13
|
作者
Chen, Bih-Cheng [1 ]
Shibu, Marthandam Asokan [2 ]
Kuo, Chia-Hua [3 ]
Shen, Chia-Yao [4 ]
Chang-Lee, Shu Nu [5 ]
Lai, Chao-Hung [6 ]
Chen, Ray-Jade [7 ]
Yao, Chun-Hsu [8 ]
Viswanadha, Vijaya Padma [9 ]
Liu, Jian-Shen [10 ,11 ]
Chen, Wei-Kung [1 ]
Huang, Chih-Yang [2 ,12 ,13 ]
机构
[1] China Med Univ, Sch Postbaccalaureate Chinese Med, Taichung, Taiwan
[2] China Med Univ, Grad Inst Basic Med Sci, Taichung, Taiwan
[3] Univ Taipei, Lab Exercise Biochem, Taipei, Taiwan
[4] Meiho Univ, Dept Nursing, Pingtung, Taiwan
[5] Asia Univ, Dept Healthcare Adm, Taichung, Taiwan
[6] Gen Hosp, Armed Force Taiclumg, Dept Internal Med, Div Cardiol, Taichung 41152, Taiwan
[7] Taipei Med Univ, Sch Med, Dept Surg, Coll Med, Taipei, Taiwan
[8] China Med Univ, Dept Biomed Imaging & Radiol Sci, Taichung, Taiwan
[9] Bharathiar Univ, Dept Biotechnol, Coimbatore 641046, Tamil Nadu, India
[10] China Med Univ, Beigang Hosp, Dept Internal Med, Div Pulm & Crit Care Med, Beigang Township, Yunlin, Taiwan
[11] China Med Univ Hosp, Dept Emergency Med, Taichung, Taiwan
[12] Asia Univ, Dept Hlth & Nutr Biotechnol, Taichung, Taiwan
[13] China Med Univ, Grad Inst Chinese Med Sci, Taichung, Taiwan
关键词
E4 promoter-binding protein 4; Hypertrophy; Angiotensin II; Calcium channels; INDUCED CARDIAC-HYPERTROPHY; LEFT-VENTRICULAR DYSFUNCTION; HYPERTENSIVE-RAT HEART; GROWTH-FACTOR-II; G-ALPHA-Q; ANGIOTENSIN-II; MYOCARDIAL-INFARCTION; GENE-EXPRESSION; TRANSCRIPTIONAL REPRESSION; BZIP FAMILY;
D O I
10.1016/j.yexcr.2018.01.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The bZIP transcription factor E4BP4 is a survival factor that is known to be elevated in diseased heart and promote cell survival. In this study the role of E4BP4 on angiotensin-II (AngII)-induced apoptosis has been examined in in vitro cell model. H9c2 cardiomyoblast cells that overexpressed E4BP4 were exposed to AngIl to observe the cardio-protective effects of E4BP4 on hypertension related apoptosis. The results from TUNEL assays revealed that E4BP4 significantly attenuated AngII-induced apoptosis. Further analysis by Western blot and RTPCR showed that E4BP4 inhibited Angll-induced IGF-II mRNA expression and cleavage of caspase-3 through the PI3K-Akt pathway. In addition, E4BP4 enhanced calcium reuptake into the sacroplasmic reticulum by down regulating PP2A and by up-regulating the phosphorylation of PKA and PLB proteins. Our findings indicate that E4BP4 functions as a survival factor in cardiomyoblasts by inhibiting IGF-II transcription and by regulating calcium cycling.
引用
收藏
页码:227 / 234
页数:8
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