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本文引用的文献

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High levels of structural diversity observed in microcystins from Microcystis CAWBG11 and characterization of six new microcystin congeners.微囊藻CAWBG11中微囊藻毒素的高水平结构多样性及六种新微囊藻毒素同系物的表征
Mar Drugs. 2014 Nov 13;12(11):5372-95. doi: 10.3390/md12115372.
2
Molecular cloning and functional characterization of a rainbow trout liver Oatp.虹鳟鱼肝有机阴离子转运多肽的分子克隆与功能特性分析
Toxicol Appl Pharmacol. 2014 Nov 1;280(3):534-42. doi: 10.1016/j.taap.2014.08.031. Epub 2014 Sep 12.
3
Molecular characterization of zebrafish Oatp1d1 (Slco1d1), a novel organic anion-transporting polypeptide.斑马鱼 Oatp1d1(Slco1d1)的分子特征,一种新型的有机阴离子转运多肽。
J Biol Chem. 2013 Nov 22;288(47):33894-33911. doi: 10.1074/jbc.M113.518506. Epub 2013 Oct 14.
4
The SLCO (former SLC21) superfamily of transporters.SLCO(原 SLC21)家族转运蛋白。
Mol Aspects Med. 2013 Apr-Jun;34(2-3):396-412. doi: 10.1016/j.mam.2012.10.009.
5
Genetics is a major determinant of expression of the human hepatic uptake transporter OATP1B1, but not of OATP1B3 and OATP2B1.遗传学是人类肝摄取转运体 OATP1B1 表达的主要决定因素,但不是 OATP1B3 和 OATP2B1 的表达的主要决定因素。
Genome Med. 2013 Jan 11;5(1):1. doi: 10.1186/gm405. eCollection 2013.
6
Investigation of microcystin congener-dependent uptake into primary murine neurons.调查微囊藻毒素同系物对原代鼠神经元的摄取。
Environ Health Perspect. 2010 Oct;118(10):1370-5. doi: 10.1289/ehp.0901289. Epub 2010 May 15.
7
The role of organic anion transporting polypeptides (OATPs/SLCOs) in the toxicity of different microcystin congeners in vitro: a comparison of primary human hepatocytes and OATP-transfected HEK293 cells.有机阴离子转运多肽(OATPs/SLCOs)在不同微囊藻毒素同系物体外毒性中的作用:原代人肝细胞和 OATP 转染的 HEK293 细胞的比较。
Toxicol Appl Pharmacol. 2010 May 15;245(1):9-20. doi: 10.1016/j.taap.2010.02.006. Epub 2010 Feb 17.
8
Molecular mechanisms of microcystin toxicity in animal cells.微囊藻毒素在动物细胞中的毒性的分子机制。
Int J Mol Sci. 2010 Jan 21;11(1):268-287. doi: 10.3390/ijms11010268.
9
Organic anion transporting polypeptides (OATP) in zebrafish (Danio rerio): Phylogenetic analysis and tissue distribution.斑马鱼(Danio rerio)中的有机阴离子转运多肽(OATP):系统发生分析和组织分布。
Comp Biochem Physiol A Mol Integr Physiol. 2010 Mar;155(3):327-35. doi: 10.1016/j.cbpa.2009.11.011. Epub 2009 Nov 25.
10
Impact of OATP transporters on pharmacokinetics.有机阴离子转运多肽(OATP)转运体对药代动力学的影响。
Br J Pharmacol. 2009 Oct;158(3):693-705. doi: 10.1111/j.1476-5381.2009.00430.x. Epub 2009 Sep 25.

斑马鱼有机阴离子转运多肽介导的微囊藻毒素同系物转运。

Zebrafish Oatp-mediated transport of microcystin congeners.

作者信息

Steiner Konstanze, Zimmermann Lisa, Hagenbuch Bruno, Dietrich Daniel

机构信息

Human and Environmental Toxicology, Department of Biology, University of Konstanz, PO BOX 662, 78457, Constance, Germany.

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

出版信息

Arch Toxicol. 2016 May;90(5):1129-39. doi: 10.1007/s00204-015-1544-3. Epub 2015 Jun 9.

DOI:10.1007/s00204-015-1544-3
PMID:26055554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4674391/
Abstract

Microcystins (MC), representing >100 congeners being produced by cyanobacteria, are a hazard for aquatic species. As MC congeners vary in their toxicity, the congener composition of a bloom primarily dictates the severity of adverse effects and appears primarily to be governed by toxicokinetics, i.e., whether transport of MCs occurs via organic anion-transporting polypeptides (Oatps). Differences in observed MC toxicity in various fish species suggest differential expression of Oatp subtypes leading to varying tissue distribution of the very same MC congener within different species. The objectives of this study were the functional characterization and analysis of the tissue distribution of Oatp subtypes in zebrafish (Danio rerio) as a surrogate model for cyprinid fish. Zebrafish Oatps (zfOatps) were cloned, and the organ distribution was determined at the mRNA level. zfOatps were transiently expressed in HEK293 cells for functional characterization using the Oatp substrates estrone-3-sulfate, taurocholate and methotrexate and specific MC congeners (MC-LR, MC-RR, MC-LF and MC-LW). Novel zfOatp isoforms were isolated. Among these isoforms, the organ-specific expression of zfOatp1d1 and of members of the zfOatp1f subfamily was identified. At the functional level, zfOatp1d1, zfOatp1f2, zfOatp1f3 and zfOatp1f4 transported at least one of the Oatp substrates, and zfOatp1d1, zfOatp1f2 and zfOatp1f4 were shown to transport MC congeners. MC-LF and MC-LW were generally transported faster than MC-LR and MC-RR. The subtype-specific expression of zfOatp1d1 and of members of the zfOatp1f subfamily as well as differences in the transport of MC congeners could explain the MC congener-dependent differences in toxicity in cyprinids.

摘要

微囊藻毒素(MC)由蓝藻产生,有100多种同系物,对水生物种构成危害。由于MC同系物的毒性各不相同,水华中同系物的组成主要决定了不良反应的严重程度,而且似乎主要受毒物动力学的控制,即MC是否通过有机阴离子转运多肽(Oatps)进行转运。在各种鱼类中观察到的MC毒性差异表明,Oatp亚型的表达存在差异,导致同一MC同系物在不同物种中的组织分布各不相同。本研究的目的是对斑马鱼(Danio rerio)中的Oatp亚型进行功能表征和组织分布分析,斑马鱼作为鲤科鱼类的替代模型。克隆了斑马鱼Oatps(zfOatps),并在mRNA水平上确定了器官分布。zfOatps在HEK293细胞中瞬时表达,使用Oatp底物硫酸雌酮、牛磺胆酸盐和甲氨蝶呤以及特定的MC同系物(MC-LR、MC-RR、MC-LF和MC-LW)进行功能表征。分离出了新的zfOatp亚型。在这些亚型中,鉴定出了zfOatp1d1和zfOatp1f亚家族成员的器官特异性表达。在功能水平上,zfOatp1d1、zfOatp1f2、zfOatp1f3和zfOatp1f4转运至少一种Oatp底物,并且zfOatp1d1、zfOatp1f2和zfOatp1f4被证明可以转运MC同系物。MC-LF和MC-LW的转运速度通常比MC-LR和MC-RR快。zfOatp1d1和zfOatp1f亚家族成员的亚型特异性表达以及MC同系物转运的差异可以解释鲤科鱼类中MC同系物依赖性的毒性差异。