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影像学神经炎症——从实验台到临床应用

Imaging Neuroinflammation - from Bench to Bedside.

作者信息

Pulli Benjamin, Chen John W

机构信息

Center for Systems Biology and Department of Radiology, Massachusetts General Hospital and Harvard Medical School, 185 Cambridge Street, Boston, MA 02114, USA.

出版信息

J Clin Cell Immunol. 2014;5. doi: 10.4172/2155-9899.1000226.

Abstract

Neuroinflammation plays a central role in a variety of neurological diseases, including stroke, multiple sclerosis, Alzheimer's disease, and malignant CNS neoplasms, among many other. Different cell types and molecular mediators participate in a cascade of events in the brain that is ultimately aimed at control, regeneration and repair, but leads to damage of brain tissue under pathological conditions. Non-invasive molecular imaging of key players in the inflammation cascade holds promise for identification and quantification of the disease process before it is too late for effective therapeutic intervention. In this review, we focus on molecular imaging techniques that target inflammatory cells and molecules that are of interest in neuroinflammation, especially those with high translational potential. Over the past decade, a plethora of molecular imaging agents have been developed and tested in animal models of (neuro)inflammation, and a few have been translated from bench to bedside. The most promising imaging techniques to visualize neuroinflammation include MRI, positron emission tomography (PET), single photon emission computed tomography (SPECT), and optical imaging methods. These techniques enable us to image adhesion molecules to visualize endothelial cell activation, assess leukocyte functions such as oxidative stress, granule release, and phagocytosis, and label a variety of inflammatory cells for cell tracking experiments. In addition, several cell types and their activation can be specifically targeted , and consequences of neuroinflammation such as neuronal death and demyelination can be quantified. As we continue to make progress in utilizing molecular imaging technology to study and understand neuroinflammation, increasing efforts and investment should be made to bring more of these novel imaging agents from the "bench to bedside."

摘要

神经炎症在多种神经疾病中起着核心作用,包括中风、多发性硬化症、阿尔茨海默病以及恶性中枢神经系统肿瘤等众多疾病。不同的细胞类型和分子介质参与大脑中的一系列事件,这些事件最终旨在控制、再生和修复,但在病理条件下会导致脑组织损伤。对炎症级联反应中的关键参与者进行非侵入性分子成像,有望在有效治疗干预为时已晚之前识别和量化疾病进程。在本综述中,我们重点关注针对神经炎症中感兴趣的炎症细胞和分子的分子成像技术,尤其是那些具有高转化潜力的技术。在过去十年中,大量分子成像剂已在(神经)炎症动物模型中得到开发和测试,其中一些已从实验室转化到临床应用。用于可视化神经炎症的最有前景的成像技术包括磁共振成像(MRI)、正电子发射断层扫描(PET)、单光子发射计算机断层扫描(SPECT)和光学成像方法。这些技术使我们能够对黏附分子进行成像以可视化内皮细胞活化,评估白细胞功能如氧化应激、颗粒释放和吞噬作用,并标记各种炎症细胞用于细胞追踪实验。此外,几种细胞类型及其活化可以被特异性靶向,并且神经炎症的后果如神经元死亡和脱髓鞘可以被量化。随着我们在利用分子成像技术研究和理解神经炎症方面不断取得进展,应该加大努力和投入,将更多这些新型成像剂从“实验室带到临床”。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5cf/4266918/322b1ce132f2/nihms620465f2.jpg

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