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A激酶锚定蛋白12A的过表达激活固醇调节元件结合蛋白-2并增强肝细胞中的胆固醇流出。

Overexpression of A-kinase anchoring protein 12A activates sterol regulatory element binding protein-2 and enhances cholesterol efflux in hepatic cells.

作者信息

Choi Moon-Chang, Lee Yang-Ui, Kim Sung-Hak, Lee Ju-Hee, Park Jung-Hyun, Streb Jeffrey W, Oh Do-Youn, Im Seock-Ah, Kim Tae-You, Jong Hyun-Soon, Bang Yung-Jue

机构信息

Laboratory for Cancer Epigenetics and Experimental Therapeutics, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.

出版信息

Int J Biochem Cell Biol. 2008;40(11):2534-43. doi: 10.1016/j.biocel.2008.04.020. Epub 2008 May 20.

Abstract

A-kinase anchoring protein 12 (AKAP12) is known to function as a scaffold protein and as a putative tumor suppressor. However, little is known about the biological role of AKAP12 in hepatic cells. In this study, we performed micro-array analysis to identify the downstream pathway of AKAP12A, and found that AKAP12A overexpression up-regulates the expressions of several cholesterol-associated genes including HMG-CoA reductase and LDL receptor, which have been reported to be controlled by sterol regulatory element binding protein-2 (SREBP-2). It was found that AKAP12A activates SREBP-2 in hepatic cells, as demonstrated by the presence of its cleavage product, whereas the activation of sterol regulatory element binding protein-1 was not remarkably changed. Moreover, AKAP12A-induced SREBP-2 activation was found to depend on SREBP cleavage-activating protein (SCAP), as inhibition of SCAP by RNAi or sterols blocked SREBP-2 activation in response to AKAP12A overexpression. Interestingly, the hydrophobic amine U18666A caused dramatic movement of AKAP12A from the plasma membrane to cytosol and lysosomal membranes. Moreover, cholesterol depletion from the plasma membrane (using methyl-beta-cyclodextrin) caused a shift of AKAP12A from the plasma membrane to the cytoplasm. Cholesterol binding assay revealed that the N-terminal region of AKAP12A binds directly to cholesterol in vitro. Furthermore, AKAP12A overexpression enhanced [3H]-cholesterol efflux to extracellular acceptors, suggesting that AKAP12A may activate SREBP-2 by increasing cholesterol efflux. In conclusion, the present study suggests that AKAP12A is a novel regulator of cellular cholesterol metabolism.

摘要

A激酶锚定蛋白12(AKAP12)已知作为一种支架蛋白和假定的肿瘤抑制因子发挥作用。然而,关于AKAP12在肝细胞中的生物学作用知之甚少。在本研究中,我们进行了微阵列分析以鉴定AKAP12A的下游途径,发现AKAP12A的过表达上调了几个与胆固醇相关的基因的表达,包括HMG-CoA还原酶和低密度脂蛋白受体,据报道这些基因受固醇调节元件结合蛋白-2(SREBP-2)控制。结果发现,AKAP12A在肝细胞中激活SREBP-2,这可通过其裂解产物的存在得到证明,而固醇调节元件结合蛋白-1的激活没有明显变化。此外,发现AKAP12A诱导的SREBP-2激活依赖于SREBP裂解激活蛋白(SCAP),因为RNA干扰或固醇对SCAP的抑制阻断了响应AKAP12A过表达的SREBP-2激活。有趣的是,疏水胺U18666A导致AKAP12A从质膜剧烈移动到细胞质和溶酶体膜。此外,从质膜去除胆固醇(使用甲基-β-环糊精)导致AKAP12A从质膜转移到细胞质。胆固醇结合试验表明,AKAP12A的N末端区域在体外直接与胆固醇结合。此外,AKAP12A的过表达增强了[3H]-胆固醇向细胞外受体的流出,表明AKAP12A可能通过增加胆固醇流出而激活SREBP-2。总之,本研究表明AKAP12A是细胞胆固醇代谢的一种新型调节因子。

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