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大鼠中固醇半转运体基因ABCG5和ABCG8的表达与调控

Expression and regulation of the sterol half-transporter genes ABCG5 and ABCG8 in rats.

作者信息

Dieter Matthew Z, Maher Jonathan M, Cheng Xingguo, Klaassen Curtis D

机构信息

Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, KS 66160, USA.

出版信息

Comp Biochem Physiol C Toxicol Pharmacol. 2004 Dec;139(4):209-18. doi: 10.1016/j.cca.2004.11.002.

Abstract

The ABCG5 and ABCG8 genes encode half-transporter proteins that heterodimerize to form a transporter of plant sterols and cholesterol. The purpose of this study was to examine the expression and regulation of ABCG5 and ABCG8 at the mRNA level in Sprague-Dawley rats. Both ABCG5 and ABCG8 mRNA were expressed primarily in rat small intestine and liver, and gender-specific differences in expression were observed. The effects of treatment with a battery of microsomal enzyme inducers on ABCG5 and ABCG8 mRNA were examined; most treatments had no effect, but of three PXR ligands, PCN was an effective inducer, spironolactone was repressive, and dexamethasone was ineffective. The effects of a 1% cholesterol diet on the regulation of rat ABCG5 and ABCG8 were also examined, and compared with those in C57BL/6 mice. Cholesterol caused a suppression of ABCG5 and ABCG8 mRNA in rat liver, but the same treatment increased the expression of these genes in mouse liver. ABCG5 and ABCG8 mRNA was also induced by cholesterol in rat ileum, but not mouse ileum. These results suggest variation between rats and mice in regulatory mechanisms controlling ABCG5 and ABCG8 expression, and may explain some differences in lipid metabolism observed between these two species.

摘要

ABCG5和ABCG8基因编码半转运蛋白,这些蛋白会异源二聚化形成植物甾醇和胆固醇的转运体。本研究的目的是检测Sprague-Dawley大鼠中ABCG5和ABCG8在mRNA水平的表达及调控情况。ABCG5和ABCG8 mRNA主要在大鼠小肠和肝脏中表达,且观察到了表达上的性别差异。研究了一系列微粒体酶诱导剂处理对ABCG5和ABCG8 mRNA的影响;大多数处理无作用,但在三种孕烷X受体(PXR)配体中,苯巴比妥钠是一种有效的诱导剂,螺内酯具有抑制作用,地塞米松则无效。还研究了1%胆固醇饮食对大鼠ABCG5和ABCG8调控的影响,并与C57BL/6小鼠进行了比较。胆固醇导致大鼠肝脏中ABCG5和ABCG8 mRNA受到抑制,但相同处理会增加小鼠肝脏中这些基因的表达。胆固醇也会诱导大鼠回肠中ABCG5和ABCG8 mRNA的表达,但不会诱导小鼠回肠中的表达。这些结果表明大鼠和小鼠在控制ABCG5和ABCG8表达的调控机制上存在差异,这可能解释了在这两个物种之间观察到的脂质代谢的一些差异。

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