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mTOR 在脂质生物合成中的新作用。

An emerging role of mTOR in lipid biosynthesis.

机构信息

Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, MA 02142, USA.

出版信息

Curr Biol. 2009 Dec 1;19(22):R1046-52. doi: 10.1016/j.cub.2009.09.058.


DOI:10.1016/j.cub.2009.09.058
PMID:19948145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3390254/
Abstract

Lipid biosynthesis is essential for the maintenance of cellular homeostasis. The lipids produced by cells (glycerolipids, fatty acids, phospholipids, cholesterol, and sphingolipids) are used as an energy source/reserve, as building blocks for membrane biosynthesis, as precursor molecules for the synthesis of various cellular products, and as signaling molecules. Defects in lipid synthesis or processing contribute to the development of many diseases, including obesity, insulin resistance, type 2 diabetes, non-alcoholic fatty liver disease, and cancer. Studies published over the last few years have shown that the target of rapamycin (TOR), a conserved serine/threonine kinase with an important role in regulating cell growth, controls lipid biosynthesis through various mechanisms. Here, we review these findings and briefly discuss their potential relevance for human health and disease.

摘要

脂质生物合成对于维持细胞内环境稳定至关重要。细胞产生的脂质(甘油磷脂、脂肪酸、磷脂、胆固醇和鞘脂)可用作能量源/储备、膜生物合成的构建模块、各种细胞产物合成的前体分子以及信号分子。脂质合成或加工的缺陷会导致多种疾病的发生,包括肥胖症、胰岛素抵抗、2 型糖尿病、非酒精性脂肪肝和癌症。过去几年发表的研究表明,雷帕霉素靶蛋白(TOR)是一种保守的丝氨酸/苏氨酸激酶,在调节细胞生长方面具有重要作用,它通过多种机制控制脂质生物合成。在这里,我们回顾了这些发现,并简要讨论了它们对人类健康和疾病的潜在相关性。

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本文引用的文献

[1]
Insulin stimulates adipogenesis through the Akt-TSC2-mTORC1 pathway.

PLoS One. 2009-7-10

[2]
mTOR complex 2 in adipose tissue negatively controls whole-body growth.

Proc Natl Acad Sci U S A. 2009-6-16

[3]
Ku-0063794 is a specific inhibitor of the mammalian target of rapamycin (mTOR).

Biochem J. 2009-6-12

[4]
New insights into mTOR signaling: mTORC2 and beyond.

Sci Signal. 2009-4-21

[5]
Rictor/TORC2 regulates Caenorhabditis elegans fat storage, body size, and development through sgk-1.

PLoS Biol. 2009-3-3

[6]
Rictor/TORC2 regulates fat metabolism, feeding, growth, and life span in Caenorhabditis elegans.

Genes Dev. 2009-2-15

[7]
Active-site inhibitors of mTOR target rapamycin-resistant outputs of mTORC1 and mTORC2.

PLoS Biol. 2009-2-10

[8]
An ATP-competitive mammalian target of rapamycin inhibitor reveals rapamycin-resistant functions of mTORC1.

J Biol Chem. 2009-3-20

[9]
A new player in the orchestra of cell growth: SREBP activity is regulated by mTORC1 and contributes to the regulation of cell and organ size.

Biochem Soc Trans. 2009-2

[10]
Adipose-specific knockout of raptor results in lean mice with enhanced mitochondrial respiration.

Cell Metab. 2008-11

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