首页> 外文期刊>Biochemical and Biophysical Research Communications >Organic anion transporter 1 (OAT1/SLC22A6) enhances bioluminescence based on d -luciferin–luciferase reaction in living cells by facilitating the intracellular accumulation of d -luciferin
【24h】

Organic anion transporter 1 (OAT1/SLC22A6) enhances bioluminescence based on d -luciferin–luciferase reaction in living cells by facilitating the intracellular accumulation of d -luciferin

机译:通过促进D -Luciferin的细胞内积聚,基于活细胞的D -Luciferin-Luciferase反应增强生物发光,通过促进D -Lucififerin的细胞内积聚来增强生物发光

获取原文
获取原文并翻译 | 示例
       

摘要

Abstract Bioluminescence (BL) imaging based on d -luciferin ( d -luc)–luciferase reaction allows noninvasive and real-time monitoring of luciferase-expressing cells. Because BL intensity depends on photons generated through the d -luc–luciferase reaction, an approach to increase intracellular levels of d -luc could improve the detection sensitivity. In the present study, we showed that organic anion transporter 1 (OAT1) is useful, as a d -luc transporter, in boosting the BL intensity in luciferase-expressing cells. Functional screening of several transporters showed that the expression of OAT1 in HEK293?cells stably expressing Pyrearinus termitilluminans luciferase (HEK293/eLuc) markedly enhanced BL intensity in the presence of d -luc. When OAT1 was transiently expressed in HEK293?cells, intracellular accumulation of d -luc was higher than that in control cells, and the specific d -luc uptake mediated by OAT1 was saturable with a Michaelis constant (K m ) of 0.23?μM. The interaction between OAT1 and d -luc was verified using 6-carboxyfluorescein, a typical substrate of OAT1, which showed that d -luc inhibited the uptake of 6-carboxyfluorescein mediated by OAT1. BL intensity was concentration-dependent at steady states in HEK293/eLuc cells stably expressing OAT1, and followed Michaelis–Menten kinetics with an apparent K m of 0.36?μM. In addition, the enhanced BL was significantly inhibited by OAT1-specific inhibitors. Thus, OAT1-mediated transport of d -luc could be a rate-limiting step in the d -luc–luciferase reaction. Furthermore, we found that expressing OAT1 in HEK293/eLuc cells implanted subcutaneously in mice also significantly increased the BL after intraperitoneal injection of d -luc. Our findings suggest that because OAT1 is capable of transporting d -luc, it can also be used to improve visualization and monitoring of luciferase-expressing cells. Highlights ? OAT1 expression in luciferase-expressing cells enhanced bioluminescence via the d -luciferin–luciferase reaction. ? OAT1 mediated the intracellular accumulation of d -luciferin. ? OAT1 increased visualization sensitivity of the bioluminescence emitted by the luciferase-expressing cells.
机译:摘要基于D -Luciferin(D -LUC)(D-LUC)的成像(B BL)成像 - 升性酶反应允许对荧光素酶的细胞进行非侵入性和实时监测。因为BL强度取决于通过D -LUC-荧光素酶反应产生的光子,所以提高D -LUC的细胞内水平的方法可以改善检测灵敏度。在本研究中,我们表明有机阴离子转运蛋白1(OAT1)作为D -LUC转运蛋白是有用的,以促进表达荧光素酶的细胞中的BL强度。几种转运蛋白的功能筛选表明,HEK293中的OAT1的表达稳定表达Pyrearinus inciruminis含有荧光素酶(HEK293 / eluc)的细胞在D -Luc存在下显着提高了Bl强度。当在HEK293中瞬时表达OAT1时,D -LUC的细胞内积累高于对照细胞中的,并且由OAT1介导的特异性D -LUC摄取与0.23Ω·μm的Michaelis常数(K m)均可饱和。使用6 - CarboxyFluoresce鉴定OAT1和D -LUC之间的相互作用,oat1的典型底物验证,其显示D -luc抑制由OAT1介导的6-羧基荧光素的摄取。 BL强度浓度依赖于HEK293 / ELUC细胞中的稳定状态,稳定地表达OAT1,并遵循MICHAELIS-MENTEN动力学,表观km为0.36Ωμm。此外,通过OAT1特异性抑制剂显着抑制增强的BL。因此,DAT1介导的D -LUC的迁移可能是D -LUC-荧光素酶反应中的速率限制步骤。此外,我们发现在小鼠中皮下植入小鼠的HEK293 /烯烃细胞中的表达OAT1也显着增加了D -LUC腹膜内注射后的BL。我们的研究结果表明,因为OAT1能够运输D -LUC,它也可用于改善表达荧光素酶的细胞的可视化和监测。强调 ? oat1在荧光素酶的表达细胞中的表达通过D -luciferin-luciferase反应增强生物发光。还OAT1介导D -Luciferin的细胞内积累。还OAT1增加了荧光素酶表达细胞发出的生物发光的可视化敏感性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号