利用内源性细胞蛋白进行分子成像。

Pub Date : 2013-01-01
Zhou Jinyuan, Hong Xiaohua
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引用次数: 0

摘要

酰胺质子转移(APT)成像是一种基于组织内源性细胞蛋白产生图像对比度的新型分子MRI技术。理论上,APT-MRI信号主要取决于可移动的酰胺质子浓度和酰胺质子交换率(与组织pH值有关)。APT技术已被用于脑卒中(pH值下降)的无创pH成像和肿瘤(许多蛋白质过表达)的蛋白质含量成像。值得注意的是,最近在动物模型中已经证明,APT-MRI信号是区分放射性坏死和活动性肿瘤的独特成像生物标志物。本文将简要介绍APT成像的基本原理,并综述其在脑卒中和脑肿瘤动物模型及患者成像中的成功应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Imaging Using Endogenous Cellular Proteins.

Amide proton transfer (APT) imaging is a novel molecular MRI technique that generates image contrast based on endogenous cellular proteins in tissue. Theoretically, the APT-MRI signal depends primarily on the mobile amide proton concentration and amide proton exchange rates (which are related to tissue pH). The APT technique has been used for non-invasive pH imaging in stroke (where pH drops) and protein content imaging in tumor (where many proteins are overexpressed). Notably, it has been recently demonstrated in animal models that the APT-MRI signal is a unique imaging biomarker to distinguish between radiation necrosis and active tumor. In this paper, we will briefly introduce the basic principle of APT imaging and review its current successful applications for the imaging of stroke and the imaging of brain tumors in animal models and in patients.

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