Department of Cell Biology, SUNY Downstate Medical Center, Brooklyn, New York 11203, USA.
J Biol Chem. 2013 Jul 12;288(28):20464-76. doi: 10.1074/jbc.M113.473454. Epub 2013 May 31.
We have shown previously that Clock, microsomal triglyceride transfer protein (MTP), and nocturnin are involved in the circadian regulation of intestinal lipid absorption. Here, we clarified the role of apolipoprotein AIV (apoAIV) in the diurnal regulation of plasma lipids and intestinal lipid absorption in mice. Plasma triglyceride in apoAIV(-/-) mice showed diurnal variations similar to apoAIV(+/+) mice; however, the increases in plasma triglyceride at night were significantly lower in these mice. ApoAIV(-/-) mice absorbed fewer lipids at night and showed blunted response to daytime feeding. To explain reasons for these lower responses, we measured MTP expression; intestinal MTP was low at night, and its induction after food entrainment was less in apoAIV(-/-) mice. Conversely, apoAIV overexpression increased MTP mRNA in hepatoma cells, indicating transcriptional regulation. Mechanistic studies revealed that sequences between -204/-775 bp in the MTP promoter respond to apoAIV and that apoAIV enhances expression of FoxA2 and FoxO1 transcription factors and their binding to the identified cis elements in the MTP promoter at night. Knockdown of FoxA2 and FoxO1 abolished apoAIV-mediated MTP induction. Similarly, knockdown of apoAIV in differentiated Caco-2 cells reduced MTP, FoxA2, and FoxO1 mRNA levels, cellular MTP activity, and media apoB. Moreover, FoxA2 and FoxO1 expression showed diurnal variations, and their expression was significantly lower in apoAIV(-/-) mice. These data indicate that apoAIV modulates diurnal changes in lipid absorption by regulating forkhead transcription factors and MTP and that inhibition of apoAIV expression might reduce plasma lipids.
我们之前已经表明,Clock、微粒体甘油三酯转移蛋白(MTP)和夜蛋白参与了肠道脂质吸收的昼夜节律调节。在这里,我们阐明了载脂蛋白 AIV(apoAIV)在小鼠血浆脂质和肠道脂质吸收的昼夜调节中的作用。apoAIV(-/-) 小鼠的血浆甘油三酯呈现出与 apoAIV(+/+) 小鼠相似的昼夜变化;然而,这些小鼠夜间血浆甘油三酯的增加明显较低。apoAIV(-/-) 小鼠夜间吸收的脂质较少,对白天进食的反应也减弱。为了解释这些较低反应的原因,我们测量了 MTP 的表达;肠道 MTP 在夜间较低,其在食物诱导后的诱导作用在 apoAIV(-/-) 小鼠中较弱。相反,apoAIV 的过表达增加了肝癌细胞中的 MTP mRNA,表明转录调节。机制研究表明,MTP 启动子中的-204/-775 bp 序列对 apoAIV 有反应,apoAIV 增强了 FoxA2 和 FoxO1 转录因子的表达,并在夜间与鉴定的 MTP 启动子顺式元件结合。FoxA2 和 FoxO1 的敲低消除了 apoAIV 介导的 MTP 诱导。同样,分化的 Caco-2 细胞中 apoAIV 的敲低降低了 MTP、FoxA2 和 FoxO1 mRNA 水平、细胞 MTP 活性和介质 apoB。此外,FoxA2 和 FoxO1 的表达呈现昼夜变化,在 apoAIV(-/-) 小鼠中表达明显较低。这些数据表明,apoAIV 通过调节叉头转录因子和 MTP 来调节脂质吸收的昼夜变化,并且抑制 apoAIV 的表达可能会降低血浆脂质。