Luu Winnie, Sharpe Laura J, Stevenson Julian, Brown Andrew J
School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW, Australia.
Biochim Biophys Acta. 2012 Feb;1823(2):458-64. doi: 10.1016/j.bbamcr.2011.09.017. Epub 2011 Oct 8.
Akt is an essential protein kinase for cell growth, proliferation, and survival. Perturbed Akt regulation is associated with a number of human diseases, such as cancer and diabetes. Recently, evidence has emerged that Akt is involved in the regulation of the sterol-regulatory element binding proteins, which are master transcriptional regulators of lipid metabolism. This offers a means by which synthesis of new membrane can be coordinated with cell growth and proliferation. However, the link between Akt and sterol-regulatory element binding protein-2, the major isoform participating in cholesterol regulation, is relatively unexplored. In the present study, we employed insulin-like growth factor-1 as an inducer of Akt signalling, and showed that it increased sterol-regulatory element binding protein-2 activation acutely (within 1h). This insulin-like growth factor-1-induced sterol-regulatory element binding protein-2 activation was blunted when Akt was inhibited pharmacologically or molecularly with small interfering RNA. Furthermore, we employed a rapalog heterodimerisation system to specifically and rapidly activate Akt, and found that sterol-regulatory element binding protein-2 activation was increased in response to Akt activation. Together, this study provides compelling evidence that Akt contributes to the acute regulation of cholesterol metabolism through activating sterol-regulatory element binding protein-2.
Akt是细胞生长、增殖和存活所必需的蛋白激酶。Akt调节紊乱与多种人类疾病相关,如癌症和糖尿病。最近,有证据表明Akt参与了固醇调节元件结合蛋白的调节,而固醇调节元件结合蛋白是脂质代谢的主要转录调节因子。这提供了一种新膜合成与细胞生长和增殖相协调的方式。然而,Akt与参与胆固醇调节的主要亚型固醇调节元件结合蛋白-2之间的联系相对较少被探索。在本研究中,我们使用胰岛素样生长因子-1作为Akt信号的诱导剂,并表明它能迅速(在1小时内)增加固醇调节元件结合蛋白-2的激活。当用药物或小分子干扰RNA在分子水平上抑制Akt时,这种胰岛素样生长因子-1诱导的固醇调节元件结合蛋白-2激活会减弱。此外,我们使用雷帕霉素类似物异二聚化系统特异性地快速激活Akt,并发现固醇调节元件结合蛋白-2的激活会随着Akt的激活而增加。总之,本研究提供了令人信服的证据,表明Akt通过激活固醇调节元件结合蛋白-2对胆固醇代谢进行急性调节。