Tabuchi Yoshiaki, Takasaki Ichiro, Doi Takeshi, Ishii Yoshiyuki, Sakai Hideki, Kondo Takashi
Division of Molecular Genetics Research, Life Science Research Center, University of Toyama, Toyama 930-0194, Japan.
FEBS Lett. 2006 May 29;580(13):3035-41. doi: 10.1016/j.febslet.2006.04.048. Epub 2006 Apr 27.
We performed microarray and computational gene network analyses to identify the detailed mechanisms by which sodium butyrate (SB) induces cell growth arrest and the differentiation of mouse colonic epithelial MCE301 cells. Two thousand six hundred four differentially expressed probe sets were identified in the cells treated with 2mM SB and were classified into four groups. Of these, the gradually increased group and the gradually and remarkably decreased group contained the genetic networks for cellular development and cell cycles or canonical pathways for fatty acid biosynthesis and pyrimidine metabolism, respectively. The present results provide a basis for understanding the detailed molecular mechanisms of action of SB in colonic epithelial cells.
我们进行了微阵列和计算基因网络分析,以确定丁酸钠(SB)诱导小鼠结肠上皮MCE301细胞生长停滞和分化的详细机制。在用2mM SB处理的细胞中鉴定出2604个差异表达的探针集,并将其分为四组。其中,逐渐增加组和逐渐显著减少组分别包含细胞发育和细胞周期的遗传网络或脂肪酸生物合成和嘧啶代谢的经典途径。本研究结果为理解SB在结肠上皮细胞中的详细分子作用机制提供了依据。