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白细胞介素-6在急性期反应期间调节肝脏转运蛋白。

Interleukin-6 regulates hepatic transporters during acute-phase response.

作者信息

Siewert Elmar, Dietrich Christoph G, Lammert Frank, Heinrich Peter C, Matern Siegfried, Gartung Carsten, Geier Andreas

机构信息

Department of Internal Medicine III, Aachen University (RWTH), Aachen, Germany.

出版信息

Biochem Biophys Res Commun. 2004 Sep 10;322(1):232-8. doi: 10.1016/j.bbrc.2004.07.102.

Abstract

Cholestasis develops during inflammatory conditions characterized by the release of cytokines like interleukin-6 (IL-6), which is the major player in the hepatic acute-phase response. However, the exact contribution of IL-6 to transporter down-regulation is unclear. Therefore, we compared wild-type and IL-6-deficient mice after IL-6-injection and induction of an aseptic (turpentine-injection) or septic (LPS-injection) acute-phase response. Down-regulation of basolateral (Ntcp, Oatp1, and Mrp3) and canalicular (Mrp2, Bsep) transporter mRNA occurred after treatment with IL-6, turpentine, and LPS. In IL-6-deficient mice, turpentine failed to decrease mRNA-levels of basolateral and canalicular transporters, whereas LPS-mediated down-regulation of Ntcp, Mrp3, and Mrp2 was abolished at later time points (24 h). In conclusion, induction of an aseptic and septic acute-phase response leads to the down-regulation of basolateral and canalicular organic anion transporters. IL-6 is required for transporter down-regulation during aseptic inflammation. Furthermore, IL-6 also contributes to transporter regulation during LPS-induced cholestasis at more delayed time points.

摘要

胆汁淤积在以白细胞介素-6(IL-6)等细胞因子释放为特征的炎症状态下发生,IL-6是肝脏急性期反应的主要参与者。然而,IL-6对转运体下调的确切作用尚不清楚。因此,我们比较了注射IL-6并诱导无菌(松节油注射)或脓毒症(脂多糖注射)急性期反应后的野生型和IL-6缺陷型小鼠。用IL-6、松节油和脂多糖处理后,基底外侧(Ntcp、Oatp1和Mrp3)和胆小管(Mrp2、Bsep)转运体mRNA发生下调。在IL-6缺陷型小鼠中,松节油未能降低基底外侧和胆小管转运体的mRNA水平,而脂多糖介导的Ntcp、Mrp3和Mrp2下调在后期时间点(24小时)被消除。总之,无菌和脓毒症急性期反应的诱导导致基底外侧和胆小管有机阴离子转运体的下调。在无菌性炎症期间,IL-6是转运体下调所必需的。此外,在脂多糖诱导的胆汁淤积后期,IL-6也参与转运体的调节。

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