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胆固醇调节人类肠道钠依赖性胆汁酸转运蛋白。

Cholesterol modulates human intestinal sodium-dependent bile acid transporter.

作者信息

Alrefai Waddah A, Sarwar Zaheer, Tyagi Sangeeta, Saksena Seema, Dudeja Pradeep K, Gill Ravinder K

机构信息

Section of Digestive Diseases and Nutrition, Department of Medicine, University of Illinois at Chicago and Jesse Brown Veteran Affairs Medical Center, Medical Research Service (600/151 820 South Damen Ave., Chicago, Illinois 60612, USA.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2005 May;288(5):G978-85. doi: 10.1152/ajpgi.00379.2004. Epub 2004 Dec 16.

Abstract

Bile acids are efficiently absorbed from the intestinal lumen via the ileal apical sodium-dependent bile acid transporter (ASBT). ASBT function is essential for maintenance of cholesterol homeostasis in the body. The molecular mechanisms of the direct effect of cholesterol on human ASBT function and expression are not entirely understood. The present studies were undertaken to establish a suitable in vitro experimental model to study human ASBT function and its regulation by cholesterol. Luminal membrane bile acid transport was evaluated by the measurement of sodium-dependent 3H-labeled taurocholic acid (3H-TC) uptake in human intestinal Caco-2 cell monolayers. The relative abundance of human ASBT (hASBT) mRNA was determined by real-time PCR. Transient transfection and luciferase assay techniques were employed to assess hASBT promoter activity. Caco-2 cell line was found to represent a suitable model to study hASBT function and regulation. 25-Hydroxycholesterol (25-HCH; 2.5 microg/ml for 24 h) significantly inhibited Na(+)-dependent 3H-TC uptake in Caco-2 cells. This inhibition was associated with a 50% decrease in the V(max) of the transporter with no significant changes in the apparent K(m). The inhibition in hASBT activity was associated with reduction in both the level of hASBT mRNA and its promoter activity. Our data show the inhibition of hASBT function and expression by 25-HCH in Caco-2 cells. These data provide novel evidence for the direct regulation of human ASBT function by cholesterol and suggest that this phenomenon may play a central role in cholesterol homeostasis.

摘要

胆汁酸通过回肠顶端钠依赖性胆汁酸转运体(ASBT)从肠腔中被高效吸收。ASBT的功能对于维持体内胆固醇稳态至关重要。胆固醇对人类ASBT功能和表达的直接作用的分子机制尚未完全明确。本研究旨在建立一个合适的体外实验模型,以研究人类ASBT的功能及其受胆固醇的调节。通过测量人肠道Caco-2细胞单层中钠依赖性3H标记牛磺胆酸(3H-TC)的摄取来评估肠腔膜胆汁酸转运。通过实时PCR测定人类ASBT(hASBT)mRNA的相对丰度。采用瞬时转染和荧光素酶测定技术评估hASBT启动子活性。发现Caco-2细胞系是研究hASBT功能和调节的合适模型。25-羟基胆固醇(25-HCH;2.5μg/ml,作用24小时)显著抑制Caco-2细胞中Na(+)-依赖性3H-TC摄取。这种抑制与转运体的V(max)降低50%相关,而表观K(m)无显著变化。hASBT活性的抑制与hASBT mRNA水平及其启动子活性的降低相关。我们的数据显示25-HCH在Caco-2细胞中抑制hASBT功能和表达。这些数据为胆固醇对人类ASBT功能的直接调节提供了新证据,并表明这种现象可能在胆固醇稳态中起核心作用。

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