期刊文献+

转录因子EB在调控脂质代谢中的研究进展

The research advances of transcription factor EB in the regulation of lipid metabolism
在线阅读 下载PDF
导出
摘要 转录因子EB(TFEB)属于小眼畸形相关转录因子(MiTF/TFE)家族,是溶酶体功能和自噬的主要调节因子,其通过调节溶酶体内脂质降解、脂肪酸β氧化以及胞内胆固醇流出等途径在调节脂质代谢过程中发挥重要作用。TFEB主要通过介导自噬以及脂质代谢相关因子的表达抑制非酒精性脂肪性肝病和肥胖症的发生,另外通过抑制巨噬细胞和血管平滑肌细胞内脂质蓄积而抑制泡沫细胞的形成延缓动脉粥样硬化的进展,还可通过促进脂噬降低脂质积累及其诱导的胰岛素抵抗与β细胞衰竭进而缓解糖尿病脂质代谢紊乱。总之,TFEB在脂质代谢过程及脂质代谢紊乱相关疾病中发挥关键作用,并可在临床上作为潜在的干预靶点以纠正体内脂质代谢紊乱。 Transcription factor EB(TFEB),which belongs to the microphthalmia/transcription factor E(MiTF/TFE)family,is mainly functioned as regulator involved in regulating lysosomal function and autophagy.It plays an important role in lipid metabolism via modulating lysosomal lipid degradation,mitochondrial β-oxidation of fatty acid,and intracellular cholesterol efflux.TFEB inhibits the development of metabolic associated fatty liver disease(MAFLD)and obesity by regulating the autophagy and the expression of lipid metabolism-related genes.Additionally,it prevents the formation of foam cell from macrophages and vascular smooth muscle cells by restraining lipid accumulation,thereby attenuating the progression of atherosclerosis.TFEB promotes lipophagy to relieve lipid accumulation and lipid accumulation-induced insulin resistance,and β-cell failure,deferring diabetes-related lipid metabolic disorders.In summary,TFEB plays a key role in lipid metabolism and associated lipid disorder diseases,and serves as a potential clinical target to correct lipid dysmetabolism in vivo.
作者 李慧娟 王云 邝彤东 吕运成 LI Huijuan;WANG Yun;KUANG Tongdong;LYU Yuncheng(Guangxi Key Laboratory of Diabetic System Medicine,Guilin Medical University,Guilin,Guangxi 541199,China)
出处 《中国动脉硬化杂志》 2025年第5期378-384,394,共8页 Chinese Journal of Arteriosclerosis
基金 国家自然科学基金项目(82160098) 广西壮族自治区自然科学基金项目(2019JJA140728)。
关键词 转录因子EB 脂质代谢 代谢相关脂肪性肝病 动脉粥样硬化 肥胖症 transcription factor EB lipid metabolism metabolic associated fatty liver disease atherosclerosis obesity
  • 相关文献

参考文献5

二级参考文献27

  • 1Russell DW. The enzymes, regulation, and genetics of bile acid syn- thesis[ J]. Annu Rev. Biochem,2003,72 : 137 - 174.
  • 2Payne AH, Hales DB. Overview of steroidogenie enzymes in the path- way from cholesterol to active steroid hormones[ J]. Endocr Rev ,200g, 25:947 - 970.
  • 3Grundy SM. Absorption and metabolism of dietary cholesterol[J]. Ann Rev Nutr, 1983,3:71 -96.
  • 4Maxfield FR,Tabas I. Role of cholesterol and lipid organization in dis- ease[ J]. Nature,2005,438:612 -621.
  • 5Bosner MS, Lange LG, Stenson WF, et al. Percent cholesterol absorp- tion in normal women and men quantified with dual stable isotopic trac- ers and negative ion mass spectrometry [ J ]. J Lipid Res, 1999,40: 302 - 308.
  • 6Altmann SW, Davis HR Jr, Zhu Ll,et al. Niemann-Piek C1 Like I pro- tein is critical for intestinal cholesterol absorption [ J ]. Science, 2004, 303 : 1201 - 1204.
  • 7Davis HR Jr, Zhu LJ, Hoos LM, et al. Niemann-Pick C1 Like 1 (NPCILI) is the intestinal phytosterol and cholesterol transporter and a key modulator of whole-body cholesterol homeostasis[ J]. J Biol Chem, 2004, 279:33586 - 33592.
  • 8Yu L, Bharadwaj S, Brown JM, et al. Cholesterol-regulated transloca- tion of NPCILI to the cell surface facilitates free cholesterol uptake[ J ]. J Biol Chem ,2006,281:6616 - 6624.
  • 9Ge L, Wang J, Qi W, et al. The cholesterol absorption inhibitor ezetimibe acts by blocking the sterol-indueed internalization of NPCIL1 [J~. Cell Metab,2008, 7:508 -519.
  • 10Ge L, Qi W, Wang LJ,et al. Flotillins play an essential role in Nie- mann-Pick Cl-like l-mediated cholesterol uptake[ J]. Proc Natl Acad Sci USA ,2011,108:551 - 556.

共引文献52

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部