Liu Zhaoqian, Dong Zizheng, Yang Zuocheng, Chen Qun, Pan Yi, Yang Youyun, Cui Ping, Zhang Xin, Zhang Jian-Ting
Department of Pharmacology and Toxicology, Walther Oncology Center, Walther Cancer Institute, Indiana University School of Medicine, 1044 W. Walnut Street, Indianapolis, IN 46202, USA.
Differentiation. 2007 Sep;75(7):652-61. doi: 10.1111/j.1432-0436.2007.00165.x. Epub 2007 Mar 23.
Eukaryotic initiation factor 3a (eIF3a) has been suggested to play a regulatory role in mRNA translation. Decreased eIF3a expression has been observed in differentiated cells while higher levels have been observed in cancer cells. However, whether eIF3a plays any role in differentiation and development is currently unknown. Here, we investigated eIF3a expression during mouse development and its role in differentiation of colon epithelial cells. We found that eIF3a expression was higher in fetal tissues compared with postnatal ones. Its expression in intestine, stomach, and lung abruptly stopped on the 18th day in gestation but persisted in liver, kidney, and heart throughout the postnatal stage at decreased levels. Similarly, eIF3a expression in colon cancer cell lines, HT-29 and Caco-2, drastically decreased prior to differentiation. Enforced eIF3a expression inhibited while knocking it down using small interference RNA promoted Caco-2 differentiation. Thus, eIF3a may play some roles in development and differentiation and that the decreased eIF3a expression may be a pre-requisite of intestinal epithelial cell differentiation.
真核生物起始因子3a(eIF3a)被认为在mRNA翻译中起调节作用。在分化细胞中观察到eIF3a表达降低,而在癌细胞中观察到较高水平的表达。然而,目前尚不清楚eIF3a在分化和发育中是否发挥任何作用。在这里,我们研究了小鼠发育过程中eIF3a的表达及其在结肠上皮细胞分化中的作用。我们发现,与出生后组织相比,胎儿组织中eIF3a的表达更高。其在肠、胃和肺中的表达在妊娠第18天突然停止,但在出生后阶段在肝脏、肾脏和心脏中持续存在,且水平降低。同样,结肠癌细胞系HT-29和Caco-2中的eIF3a表达在分化前急剧下降。强制表达eIF3a会抑制Caco-2分化,而使用小干扰RNA敲低它则会促进Caco-2分化。因此,eIF3a可能在发育和分化中发挥一些作用,并且eIF3a表达降低可能是肠上皮细胞分化的一个先决条件。