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A mitochondrial-targeting near-infrared fluorescent probe for bioimaging and evaluating endogenous superoxide anion changes during ischemia/reperfusion injury

机译:用于在缺血/再灌注损伤期间的用于生物分析和评估内源超氧化物阴离子的线粒体靶向近红外荧光探针

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Abstract The outburst of superoxide anion (O 2 ? ) in mitochondrial during ischemia/reperfusion (I/R) process will cause a series of oxidative damage including polarity loss of mitochondrial membrane potential, overload of secondary cellular calcium, and cascade apoptosis. To monitor the O 2 ? level fluctuations as well as to evaluate the relationship between O 2 ? concentration and the degree of cell apoptosis during I/R process, we propose a ratiometric near-infrared mitochondrial targeting fluorescent probe Mito-Cy-Tfs for the detection of level changes of O 2 ? in cells and in?vivo . The probe Mito-Cy-Tfs is composed of three moieties: near-infrared heptamethine cyanine as fluorescence signal transducer, trifluoromethanesulfonamide as fluorescence modulator, and lipophilic triphenylphosphonium cation as mitochondrial guider. The probe can well locate in mitochondria and respond the concentration changes of endogenous O 2 ? selectively and sensitively. The probe has been successfully utilized to image the endogenous O 2 ? fluctuations in four kinds of cell I/R models (glucose deprivation/reperfusion, serum deprivation/reperfusion, oxygen deprivation/reperfusion and glucose-serum-oxygen deprivation/reperfusion). The probe also exhibits deep tissue penetration for real-time imaging of O 2 ? concentration in liver of I/R mice model. We confirm that the adoption of ischemic preconditioning (IPC) and postconditioning (IPTC) can protect liver from I/R injury. The probe can be employed to accurately indicate and evaluate the mutual relationship between the levels of O 2 ? and the degrees of organ damage during I/R, IPC and IPTC processes. The above applications make our new probe a potential candidate for the clinical surgery assessment. Highlights ? A mitochondrial-targeting near-infrared ratiometric fluorescent probe for bioimaging during ischemia/reperfusion (I/R) injury. ? The probe can be used to evaluate the burst of endogenous superoxide anion (O 2 . ? ) in mitochondria during cell I/R process. ? Further, to explore the relationship between O 2 . ? concentration and I/R injury degree. ? Ischemic preconditioning and postconditioning can limit the degree of liver I/R injury through the decrease of O 2 . ? burst.
机译:摘要在缺血/再灌注(I / R)过程中线粒体中超氧化物阴离子(O 2?)的爆发将导致一系列氧化损伤,包括线粒体膜电位,二次细胞钙的过载和级联细胞凋亡的极性损失。监控O 2?水平波动以及评估O 2之间的关系?浓度和细胞凋亡程度在I / R过程中,我们提出了一个比例近红外线粒体靶向荧光探针MITO-CY-TFS,用于检测O 2的水平变化?在细胞和体内。探针MITO-CY-TFS由三个部分组成:近红外庚啶氰胺作为荧光信号传感器,三氟甲磺酰胺作为荧光调节剂,以及亲脂性三苯基鏻阳离子作为线粒体导向器。探针可以很好地定位在线粒体中,并响应内源O 2的浓度变化?选择性和敏感。探针已成功用于图像内源O 2?四种细胞I / R模型的波动(葡萄糖剥夺/再灌注,血清剥夺/再灌注,氧气剥夺/再灌注和葡萄糖 - 血清氧剥夺/再灌注)。探头还表现出深组织渗透以进行O 2的实时成像? I / R小鼠模型的肝脏浓度。我们确认采用缺血预处理(IPC)和后处理(IPTC)可以保护肝免受I / R损伤的影响。可以采用探针来准确地表明和评估o 2水平之间的相互关系?在I / R,IPC和IPTC进程期间的器官损坏程度。上述应用使我们的新探针成为临床外科评估的潜在候选者。强调 ?用于在缺血/再灌注(I / R)损伤期间的用于生物成像的线粒体靶向近红外测量荧光探针。还探针可用于在细胞I / R过程中评估线粒体中的内源超氧化物阴离子(O 2。Δ)的爆发。还此外,探索O 2之间的关系。还浓度和I / R损伤程度。还缺血预处理和后处理可以通过减少O 2来限制肝脏I / R损伤程度。还爆裂。

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