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使用基于荧光肽的探针在小鼠后肢缺血模型中对血管生成进行体内监测。

In vivo monitoring of angiogenesis in a mouse hindlimb ischemia model using fluorescent peptide-based probes.

作者信息

Park Subin, Lee Jangwook, Jo Mi-Hee, Na Jin Hee, Park Sung-Gurl, Jang Hyeon-Ki, Kang Sun-Woong, Kim Jong-Ho, Kim Byung-Soo, Park Jae Hyung, Kwon Ick Chan, Ryu Ju Hee, Kim Kwangmeyung

机构信息

Center for Theragnosis, Biomedical Research Institute, Korea Institute of Science and Technology, 39-1 Hawolgok-dong, Seongbuk-gu, Seoul, 136-791, Republic of Korea.

Departments of Polymer Science and Chemical Engineering, Sungkyunkwan University, Suwon, 440-746, Republic of Korea.

出版信息

Amino Acids. 2016 Jul;48(7):1641-54. doi: 10.1007/s00726-016-2225-0. Epub 2016 Apr 20.

Abstract

Vascular endothelial growth factor receptor (VEGFR) and matrix metalloproteinase (MMP) are up-regulated in ischemic tissue and play pivotal roles in promoting angiogenesis. The purpose of the present study was to evaluate two fluorophore-conjugated peptide probes specific to VEGFR and MMP for dual-targeted in vivo monitoring of angiogenesis in a murine model of hindlimb ischemia. To this end, VEGFR-Probe and MMP-Probe were developed by conjugating distinct near-infrared fluorophores to VEGFR-binding and MMP substrate peptides, respectively. VEGFR-Probe exhibited specific binding to VEGFR on HUVECs, and self-quenched MMP-Probe produced strong fluorescence intensity in the presence of MMPs in vitro. Subsequently, VEGFR-Probe and MMP-Probe were successfully utilized for time course in vivo visualization of VEGFR or MMP, respectively. Simultaneous visualization provided information regarding the spatial distribution of these proteins, including areas of co-localization. This dual-targeted in vivo imaging approach will be useful for understanding the detailed mechanism of angiogenesis and for evaluating therapeutic angiogenesis.

摘要

血管内皮生长因子受体(VEGFR)和基质金属蛋白酶(MMP)在缺血组织中上调,并在促进血管生成中起关键作用。本研究的目的是评估两种分别针对VEGFR和MMP的荧光团偶联肽探针,用于在小鼠后肢缺血模型中对血管生成进行双靶点体内监测。为此,通过将不同的近红外荧光团分别偶联到VEGFR结合肽和MMP底物肽上,开发了VEGFR探针和MMP探针。VEGFR探针在人脐静脉内皮细胞(HUVECs)上表现出与VEGFR的特异性结合,并且自猝灭的MMP探针在体外存在MMP时产生强烈的荧光强度。随后,VEGFR探针和MMP探针分别成功用于体内VEGFR或MMP的时间进程可视化。同时可视化提供了关于这些蛋白质空间分布的信息,包括共定位区域。这种双靶点体内成像方法将有助于理解血管生成的详细机制并评估治疗性血管生成。

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