Regulation and Metabolic Significance of De Novo Lipogenesis in Adipose Tissues

被引:405
作者
Song, Ziyi
Xiaoli, Alus M.
Yang, Fajun [1 ]
机构
[1] Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
基金
美国国家卫生研究院;
关键词
adipocyte; de novo lipogenesis; transcription; post-translation; central regulation; ChREBP; SREBP; LXR; FASN; obesity; insulin resistance; thermogenesis; ELEMENT-BINDING PROTEIN; FATTY-ACID SYNTHASE; DIET-INDUCED OBESITY; LIVER-X-RECEPTOR; COLD-INDUCED THERMOGENESIS; INSULIN-RESISTANCE; LXR-ALPHA; BROWN FAT; GLUCOSE-HOMEOSTASIS; HEPATIC STEATOSIS;
D O I
10.3390/nu10101383
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
De novo lipogenesis (DNL) is a complex and highly regulated process in which carbohydrates from circulation are converted into fatty acids that are then used for synthesizing either triglycerides or other lipid molecules. Dysregulation of DNL contributes to human diseases such as obesity, type 2 diabetes, and cardiovascular diseases. Thus, the lipogenic pathway may provide a new therapeutic opportunity for combating various pathological conditions that are associated with dysregulated lipid metabolism. Hepatic DNL has been well documented, but lipogenesis in adipocytes and its contribution to energy homeostasis and insulin sensitivity are less studied. Recent reports have gained significant insights into the signaling pathways that regulate lipogenic transcription factors and the role of DNL in adipose tissues. In this review, we will update the current knowledge of DNL in white and brown adipose tissues with the focus on transcriptional, post-translational, and central regulation of DNL. We will also summarize the recent findings of adipocyte DNL as a source of some signaling molecules that critically regulate energy metabolism.
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页数:22
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