eIF3 P170对发育心肌细胞周期的调控及其机制  

Regulation mechanism of eIF3 P170 on developing myocardial cell cycle

作　　者：康婷[1,2] 杨作成[1] 黄利华[1] 向红[1] 

机构地区：[1]中南大学湘雅三医院儿科,长沙410013 [2]南华大学附属第一医院儿科,湖南衡阳421000

出　　处：《中南大学学报（医学版）》2013年第11期1146-1151,共6页Journal of Central South University ：Medical Science

基　　金：中南大学研究生创新课题(2010xxts)~~

摘　　要：目的:探讨eIF3 P170,cdc2,cyclinD1,cyclinB1在小鼠发育心肌细胞细胞周期中的表达及eIF3P170与cdc2,cyclinD1,cyclinB1之间的相关关系。方法:取不同时间点小鼠心肌细胞,RT-PCR检测eIF3 P170,cdc2,cyclinD1和cyclinB1 mRNA的表达。结果:eIF3 P170,cdc2,cyclinD1和cyclinB1 mRNA的表达在胚胎第13,15,18天(G13,G15,G18)及小鼠出生后第1,2,3,5天(P1,P2,P3,P5)的表达均较强,在小鼠出生后第5天表达达到最强(P5与其他各时间点比较,P<0.05),而后表达逐渐减弱,在出生后第30天(P30)的表达降至最弱(P30与其他各时间点比较,P<0.05)。eIF3 P170与cdc2,cyclinD1和cyclinB1 mRNA表达之间具有正相关关系。结论:eIF3 P170,cdc2,cyclinD1和cyclinB1 mRNA的表达在胚胎期及出生早期均较强,在小鼠出生后第5天达到最强,之后逐渐下降。Objective：To investigate the expression of eIF3P170, cdc2, cyclinB1 and cyclinD1 in developing cardiac myocytes, and the correlation between eIF3P170 with cdc2, cyclin D1, and cyclin B1 in mice.Methods：Mouse cardiac myocytes were obtained at different time points. RT-PCR was employed to detect the expression of eIF3P170, cdc2, cyclin D1 and cyclin B1 mRNA. Results：Expressions of eIF3P170, cdc2, cyclinD1 and cyclinB1 mRNA were higher in the embryonic Day 13, 15, 18 and postnatal Day 1, 2, 3, 5. Expressions at postnatal Day 5 reached the highest （all P values Conclusion：hTe mRNA expressions of eIF3 P170, cdc2, cyclin D1 and cyclin B1 in the embryo and the early life atfer birth are high. hTey reach the maximum at postnatal Day 5, then gradually decreased.

关 键 词：eIF3P170 CDC2 CYCLIND1 CYCLINB1 细胞周期 心脏 发育 

分 类 号：R363[医药卫生—病理学]