Lee Ann-Hwee, Scapa Erez F, Cohen David E, Glimcher Laurie H
Department of Immunology and Infectious Diseases, Harvard School of Public Health, Boston, MA 02115, USA.
Science. 2008 Jun 13;320(5882):1492-6. doi: 10.1126/science.1158042.
Dietary carbohydrates regulate hepatic lipogenesis by controlling the expression of critical enzymes in glycolytic and lipogenic pathways. We found that the transcription factor XBP1, a key regulator of the unfolded protein response, is required for the unrelated function of normal fatty acid synthesis in the liver. XBP1 protein expression in mice was elevated after feeding carbohydrates and corresponded with the induction of critical genes involved in fatty acid synthesis. Inducible, selective deletion of XBP1 in the liver resulted in marked hypocholesterolemia and hypotriglyceridemia, secondary to a decreased production of lipids from the liver. This phenotype was not accompanied by hepatic steatosis or compromise in protein secretory function. The identification of XBP1 as a regulator of lipogenesis has important implications for human dyslipidemias.
膳食碳水化合物通过控制糖酵解和脂肪生成途径中关键酶的表达来调节肝脏脂肪生成。我们发现,转录因子XBP1是未折叠蛋白反应的关键调节因子,它是肝脏中正常脂肪酸合成这一不相关功能所必需的。喂食碳水化合物后,小鼠体内XBP1蛋白表达升高,且与参与脂肪酸合成的关键基因的诱导相对应。肝脏中XBP1的可诱导性、选择性缺失导致显著的低胆固醇血症和低甘油三酯血症,这是由于肝脏脂质生成减少所致。该表型不伴有肝脂肪变性或蛋白质分泌功能受损。将XBP1鉴定为脂肪生成的调节因子对人类血脂异常具有重要意义。