Yan Jun-Kai, Zhu Jie, Gong Zi-Zhen, Wen Jie, Xiao Yong-Tao, Cai Wei, Zhang Tian
Cell Physiol Biochem. 2017;41(2):711-721. doi: 10.1159/000458430. Epub 2017 Feb 8.
Parenterally-administered lipid emulsion (LE) is a key cause of enterocyte apoptosis under total parenteral nutrition, yet the pathogenesis has not been fully understood. CUGBP, Elav-like family member 1 (CELF1) has been recently identified as a crucial modulator of apoptosis, and thus this study sought to investigate its role in the LE-induced apoptosis in vitro.
Caco-2 cells were used as an in vitro model. The cells were treated with varying LEs derived from soybean oil, olive oil or fish oil, and changes in the apoptosis and CELF1 expression were assessed. Rescue study was performed using transient knockdown of CELF1 with specific siRNA prior to LE treatment. Regulation of CELF1 by LE treatment was studied using quantitative real-time PCR and Western blotting.
All the LEs up-regulated CELF1expression and induced apoptosis, but only olive oil-supplemented lipid emulsion (OOLE)-induced apoptosis was attenuated by depletion of CELF1. Up-regulation of apoptosis-inducing factor (AIF) was involved in OOLE-induced CELF1 dependent apoptosis. The protein expression of CELF1 was up-regulated by OOLE in a dose- and time-dependent manner, but the mRNA expression of CELF1 was unchanged. Analysis by polysomal profiling and nascent protein synthesis revealed that the regulation of CELF1 by OOLE treatment was mediated by directly accelerating its protein translation.
OOLE-induces apoptosis in Caco-2 cells partially through up-regulation of CELF1.
胃肠外营养时胃肠外给予的脂质乳剂(LE)是肠细胞凋亡的关键原因,但其发病机制尚未完全明确。CUGBP、Elav样家族成员1(CELF1)最近被确定为凋亡的关键调节因子,因此本研究旨在探讨其在体外LE诱导的凋亡中的作用。
采用Caco-2细胞作为体外模型。用来源于大豆油、橄榄油或鱼油的不同LE处理细胞,评估凋亡和CELF1表达的变化。在LE处理前,使用特异性siRNA瞬时敲低CELF1进行挽救研究。采用定量实时PCR和蛋白质印迹法研究LE处理对CELF1的调节作用。
所有LE均上调CELF1表达并诱导凋亡,但只有补充橄榄油的脂质乳剂(OOLE)诱导的凋亡可因CELF1缺失而减弱。凋亡诱导因子(AIF)的上调参与了OOLE诱导的CELF1依赖性凋亡。OOLE以剂量和时间依赖性方式上调CELF1的蛋白质表达,但CELF1的mRNA表达未改变。通过多核糖体分析和新生蛋白质合成分析表明,OOLE处理对CELF1的调节是通过直接加速其蛋白质翻译介导的。
OOLE部分通过上调CELF1诱导Caco-2细胞凋亡。