Lee Bonggi, Zhu Jiabin, Wolins Nathan E, Cheng Ji-Xin, Buhman Kimberly K
Department of Foods and Nutrition, Purdue University, 700 W. State Street, West Lafayette, IN 47907-2059, USA.
Biochim Biophys Acta. 2009 Dec;1791(12):1173-80. doi: 10.1016/j.bbalip.2009.08.002. Epub 2009 Aug 20.
Recently, we found that enterocytes dynamically store triglycerides (TGs) in cytoplasmic lipid droplets (CLDs) during dietary fat absorption. A dynamic pool of TG in the form of CLDs which expands and depletes relative to time post dietary fat challenge is present in the absorptive cells of the small intestine, enterocytes. To identify cellular factors which may play a role in the regulation of this dynamic process we investigated the expression and localization of a lipid droplet associated protein family, PAT proteins, in enterocytes of mice chronically and acutely challenged by dietary fat. We found that adipophilin and Tip47 are the only PAT genes present in mouse intestinal mucosa and both genes are present at higher levels after high-fat challenges. We found TIP47 protein present in the intestine from chow and high-fat challenged mice; however, adipophilin protein was only present after high-fat challenges. In addition, TIP47 protein level was higher after an acute than a chronic high-fat challenge whereas adipophilin protein level was higher after a chronic than an acute high-fat challenge. We co-imaged TG in CLDs using CARS microscopy and TIP47 or adipophilin using immunocytochemistry in isolated enterocytes from mice challenged chronically and acutely by high levels of dietary fat. TIP47, but not adipophilin, coats CLDs in enterocytes after an acute high-fat challenge suggesting that TIP47 plays a role in the synthesis of CLDs from newly synthesized TG at the beginning of the process of dietary fat absorption in enterocytes. Adipophilin, on the other hand, coats CLDs only in enterocytes of chronic high-fat fed mice suggesting that adipophilin may play a role in the stabilization of TG stored in CLDs in longer term. These results suggest distinct roles for TIP47 and adipophilin in dietary fat absorption.
最近,我们发现肠上皮细胞在膳食脂肪吸收过程中会在细胞质脂滴(CLD)中动态储存甘油三酯(TG)。在小肠的吸收细胞即肠上皮细胞中,存在一个以CLD形式存在的TG动态库,其会随着膳食脂肪刺激后的时间而扩张和消耗。为了确定可能在这一动态过程调节中发挥作用的细胞因子,我们研究了脂滴相关蛋白家族PAT蛋白在长期和急性受到膳食脂肪刺激的小鼠肠上皮细胞中的表达和定位。我们发现,脂肪亲和素和Tip47是小鼠肠黏膜中仅有的PAT基因,在高脂刺激后这两个基因的表达水平均升高。我们发现,正常饮食和高脂刺激的小鼠肠道中均存在TIP47蛋白;然而,脂肪亲和素蛋白仅在高脂刺激后出现。此外,急性高脂刺激后TIP47蛋白水平高于慢性高脂刺激,而慢性高脂刺激后脂肪亲和素蛋白水平高于急性高脂刺激。我们使用相干反斯托克斯拉曼散射(CARS)显微镜对CLD中的TG进行共成像,并使用免疫细胞化学方法对长期和急性受到高水平膳食脂肪刺激的小鼠分离出的肠上皮细胞中的TIP47或脂肪亲和素进行共成像。急性高脂刺激后,TIP47而非脂肪亲和素会覆盖肠上皮细胞中的CLD,这表明TIP47在肠上皮细胞膳食脂肪吸收过程开始时,由新合成的TG合成CLD的过程中发挥作用。另一方面,脂肪亲和素仅在慢性高脂喂养小鼠的肠上皮细胞中覆盖CLD,这表明脂肪亲和素可能在长期稳定CLD中储存的TG方面发挥作用。这些结果表明TIP47和脂肪亲和素在膳食脂肪吸收中具有不同的作用。