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血管生成的功能与分子磁共振成像:观察靶点,见证其作用过程。

Functional and molecular MR imaging of angiogenesis: seeing the target, seeing it work.

作者信息

Neeman Michal

机构信息

Department of Biological Regulation, The Weizmann Institute of Science, Rehovot 76100, Israel.

出版信息

J Cell Biochem Suppl. 2002;39:11-7. doi: 10.1002/jcb.10399.

Abstract

Intensive research over the last years led to the discovery of multiple molecular pathways and intricate regulatory network controlling the growth and regression of blood vessels in general and angiogenesis in particular. The difficulties in elucidation of the regulation of angiogenesis, stems from the inherent complexity due to participation of many cell types, under a dominant impact of physiological and environmental effects of flow, perfusion, and oxygenation. Major advances were achieved with the use of sophisticated transgenic mice models engineered so as to provide spatially and temporally controlled expression of specific factors alone or in combination. In vivo analysis of these models frequently requires the use of non-invasive imaging modalities for measurement of functional parameters of the vasculature along with dynamic molecular information. Optical methods are extensively applied for the study of angiogenesis [Brown et al., 2001] but provide very limited tissue penetration. MRI offers the advantage of being non-invasive with uniform and relatively high spatial resolution for deep tissues. Multiple MRI approaches for monitoring angiogenesis were developed over the last years, each looking at a particular step in the process. The aim of this paper is to analyze the clinical, pharmaceutical, and biological needs for imaging of angiogenesis, and to critically evaluate the strengths and weaknesses of functional and molecular imaging for monitoring angiogenesis. The inherent problem of validation of different measures of angiogenesis, and the advantages and limitations associated with application of MRI based methods, as surrogates for other measurements of angiogenesis will be discussed. The terms molecular imaging and functional imaging are frequently loosely defined with a significant overlap between the two. For the sake of this paper we will apply a narrower definition of both terms, where molecular imaging will apply to methods directed towards detection of specific biological molecules that participate directly in (regulation of) a physiological process; while functional imaging will be used to describe those methods that aim to detect the physiological response to a defined (molecular) stimulus.

摘要

过去几年的深入研究发现了多个分子途径以及复杂的调控网络,这些调控着一般血管的生长和消退,尤其是血管生成。阐明血管生成调控的困难源于其内在复杂性,这是由于多种细胞类型的参与,以及血流、灌注和氧合等生理和环境效应的主导影响。利用经过基因工程改造的复杂转基因小鼠模型取得了重大进展,这些模型能够单独或联合提供特定因子在空间和时间上的可控表达。对这些模型的体内分析通常需要使用非侵入性成像方式来测量脉管系统的功能参数以及动态分子信息。光学方法被广泛应用于血管生成的研究[Brown等人,2001年],但组织穿透深度非常有限。MRI具有非侵入性的优势,对深部组织具有均匀且相对较高的空间分辨率。在过去几年中开发了多种用于监测血管生成的MRI方法,每种方法都着眼于该过程中的特定步骤。本文的目的是分析血管生成成像的临床、药学和生物学需求,并批判性地评估用于监测血管生成的功能成像和分子成像的优缺点。将讨论血管生成不同测量方法验证的固有问题,以及基于MRI的方法作为血管生成其他测量替代方法的优缺点。分子成像和功能成像这两个术语的定义常常比较宽松,两者之间有很大重叠。在本文中,我们将对这两个术语采用更狭义的定义,其中分子成像将适用于旨在检测直接参与(调节)生理过程的特定生物分子的方法;而功能成像将用于描述那些旨在检测对特定(分子)刺激的生理反应的方法。

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