首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >Non-invasive In Vivo Fluorescence Optical Imaging of Inflammatory MMP Activity Using an Activatable Fluorescent Imaging Agent
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Non-invasive In Vivo Fluorescence Optical Imaging of Inflammatory MMP Activity Using an Activatable Fluorescent Imaging Agent

机译:使用可激活的荧光成像剂对炎症性MMP活性进行非侵入性体内荧光光学成像。

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摘要

This paper describes a non-invasive method for imaging matrix metalloproteinases (MMP)-activity by an activatable fluorescent probe, via in vivo fluorescence optical imaging (OI), in two different mouse models of inflammation: a rheumatoid arthritis (RA) and a contact hypersensitivity reaction (CHR) model. Light with a wavelength in the near infrared (NIR) window (650 - 950 nm) allows a deeper tissue penetration and minimal signal absorption compared to wavelengths below 650 nm. The major advantages using fluorescence OI is that it is cheap, fast and easy to implement in different animal models.Activatable fluorescent probes are optically silent in their inactivated states, but become highly fluorescent when activated by a protease. Activated MMPs lead to tissue destruction and play an important role for disease progression in delayed-type hypersensitivity reactions (DTHRs) such as RA and CHR. Furthermore, MMPs are the key proteases for cartilage and bone degradation and are induced by macrophages, fibroblasts and chondrocytes in response to pro-inflammatory cytokines. Here we use a probe that is activated by the key MMPs like MMP-2, -3, -9 and -13 and describe an imaging protocol for near infrared fluorescence OI of MMP activity in RA and control mice 6 days after disease induction as well as in mice with acute (1x challenge) and chronic (5x challenge) CHR on the right ear compared to healthy ears.
机译:本文介绍了一种可激活的荧光探针通过体内荧光光学成像(OI)在两种不同的炎症小鼠模型中对基质金属蛋白酶(MMP)活性进行成像的非侵入性方法:类风湿关节炎(RA)和接触超敏反应(CHR)模型。与低于650 nm的波长相比,具有在近红外(NIR)窗口(650-950 nm)中的波长的光可以实现更深的组织穿透和最小的信号吸收。使用荧光OI的主要优势在于它便宜,快速且易于在不同动物模型中实施。可激活的荧光探针在其灭活状态下是光学沉默的,但在被蛋白酶激活后变成高荧光。活化的MMP导致组织破坏,并在RA和CHR等延迟型超敏反应(DTHR)中对疾病进展起重要作用。此外,MMPs是软骨和骨降解的关键蛋白酶,是由巨噬细胞,成纤维细胞和软骨细胞对促炎性细胞因子反应诱导的。在这里,我们使用由关键MMP(如MMP-2,-3,-9和-13)激活的探针,并描述了诱发疾病6天后RA和对照小鼠MMP活性的近红外荧光OI的成像方案与健康耳朵相比,右耳患有急性(1x挑战)和慢性(5x挑战)CHR的小鼠。

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