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使用多价锌(II)-双(二吡啶甲胺)荧光探针增强细胞死亡成像。

Enhanced cell death imaging using multivalent zinc(II)-bis(dipicolylamine) fluorescent probes.

作者信息

Smith Bryan A, Harmatys Kara M, Xiao Shuzhang, Cole Erin L, Plaunt Adam J, Wolter William, Suckow Mark A, Smith Bradley D

机构信息

Department of Chemistry and Biochemistry, 236 Nieuwland Science Hall, University of Notre Dame , Notre Dame, Indiana 46556, United States.

出版信息

Mol Pharm. 2013 Sep 3;10(9):3296-303. doi: 10.1021/mp300720k. Epub 2013 Aug 5.

Abstract

There is a clinical need for imaging technologies that can accurately detect cell death in a multitude of pathological conditions. Zinc(II)-bis(dipicolylamine) (Zn2BDPA) coordination complexes are known to associate with the anionic phosphatidylserine that is exposed on the surface of dead and dying cells, and fluorescent monovalent Zn2BDPA probes are successful cell death imaging agents. This present study compared the membrane targeting ability of two structurally related deep-red fluorescent probes, bis-Zn2BDPA-SR and tetra-Zn2BDPA-SR, with two and four appended Zn2BDPA units, respectively. Vesicle and cell microscopy studies indicated that a higher number of Zn2BDPA targeting units improved probe selectivity for phosphatidylserine-rich vesicles, and increased probe localization at the plasma membrane of dead and dying cells. The fluorescent probes were also tested in three separate animal models, (1) necrotic prostate tumor rat model, (2) thymus atrophy mouse model, and (3) traumatic brain injury mouse model. In each case, there was more tetra-Zn2BDPA-SR accumulation at the site of cell death than bis-Zn2BDPA-SR. The results indicate that multivalent Zn2BDPA probes are promising molecules for effective imaging of cell death processes in cell culture and in living subjects.

摘要

临床上需要能够在多种病理状况下准确检测细胞死亡的成像技术。已知锌(II)-双(二吡啶甲胺)(Zn2BDPA)配位络合物会与死亡和濒死细胞表面暴露的阴离子磷脂酰丝氨酸结合,且荧光单价Zn2BDPA探针是成功的细胞死亡成像剂。本研究比较了两种结构相关的深红色荧光探针双-Zn2BDPA-SR和四-Zn2BDPA-SR的膜靶向能力,它们分别带有两个和四个附加的Zn2BDPA单元。囊泡和细胞显微镜研究表明,更多数量的Zn2BDPA靶向单元提高了探针对富含磷脂酰丝氨酸囊泡的选择性,并增加了探针在死亡和濒死细胞质膜上的定位。这些荧光探针还在三种不同的动物模型中进行了测试,(1)坏死性前列腺肿瘤大鼠模型,(2)胸腺萎缩小鼠模型,以及(3)创伤性脑损伤小鼠模型。在每种情况下,细胞死亡部位的四-Zn2BDPA-SR积累都比双-Zn2BDPA-SR多。结果表明,多价Zn2BDPA探针是用于在细胞培养和活体中有效成像细胞死亡过程的有前景的分子。

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