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A versatile imaging platform with fluorescence and CT imaging capabilities that detects myeloperoxidase activity and inflammation at different scales

机译:具有荧光和CT成像能力的多功能成像平台,可检测不同尺度的肌释放酶活性和炎症

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Aberrant innate immune response drives the pathophysiology of many diseases. Myeloperoxidase (MPO) is a highly oxidative enzyme secreted by activated myeloid pro-inflammatory immune cells such as neutrophils and macrophages, and is a key mediator of the damaging innate immune response. Current technologies for detecting MPO activity in living organisms are sparse and suffer from any combination of low specificity, low tissue penetration, or low spatial resolution. We describe a versatile imaging platform to detect MPO activity using an activatable construct conjugated to a biotin moiety (MPO-activatable biotinylated sensor, MABS) that allows monitoring the innate immune response and its modulation at different scales and settings. Methods: We designed and synthesized MABS that contains MPO-specific and biotin moieties, and validated its specificity and sensitivity combining with streptavidin-labeled fluorescent agent and gold nanoparticles imaging in vitro and in vivo in multiple mouse models of inflammation and infection, including Matrigel implant, dermatitis, cellulitis, cerebritis and complete Fraud's adjuvant (CFA)-induced inflammation. Results: MABS MPO imaging non-invasively detected varying MPO concentrations, MPO inhibition, and MPO deficiency in vivo with high sensitivity and specificity. MABS can be used to obtain not only a fluorescence imaging agent, but also a CT imaging agent, conferring molecular activity information to a structural imaging modality. Importantly, using this method on tissue-sections, we found that MPO enzymatic activity does not always co-localize with MPO protein detected with conventional techniques (e.g., immunohistochemistry), underscoring the importance of monitoring enzymatic activity. Conclusion: By choosing from different available secondary probes, MABS can be used to create systems suitable to investigate and image MPO activity at different scales and settings.
机译:异常先天免疫应答驱动了许多疾病的病理生理学。 MyeloceRoxiDase(MPO)是通过活化的髓样促炎免疫细胞如中性粒细胞和巨噬细胞分泌的高氧化酶,并且是损伤天生的免疫反应的关键介体。用于检测生物体中MPO活性的目前的技术稀疏,患有低特异性,低组织渗透或低空间分辨率的任何组合。我们描述了一种多功能成像平台,用于使用与生物素部分(MPO-活化的生物素化的传感器,MAb)缀合的可活化构建体来检测MPO活性,其允许在不同的尺度和设置下监测先天免疫应答及其调制。方法:我们设计和合成含有MPO特异性和生物素部分的MAB,并验证了其特异性和敏感性与三霉菌蛋白标记的荧光剂和金纳米颗粒在多种小鼠炎症和感染的体内成像,包括Matrigel植入物,皮炎,蜂窝织炎,脑炎和完全欺诈的佐剂(CFA)诱导的炎症。结果:MABS MPO成像非侵入性地检测不同的MPO浓度,MPO抑制和体内的MPO缺乏,具有高灵敏度和特异性。 MAB可用于不仅获得荧光成像剂,还可以获得CT成像剂,将分子活性信息赋予结构成像模态。重要的是,在组织部分上使用该方法,我们发现MPO酶活性并不总是与用常规技术(例如,免疫组织化学)检测的MPO蛋白共定位,强调监测酶活性的重要性。结论:通过从不同可用的二次探测中选择,MAB可用于创建适合于在不同尺度和设置下进行调查和图像MPO活动的系统。

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