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Assessing bladder hyper-permeability biomarkers in vivo using molecularly-targeted MRI

机译:使用分子靶向MRI评估体内膀胱高通透性生物标志物

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摘要

The objective was to investigate if some of the key molecular players associated with bladder hyper-permeability in interstitial cystitis/bladder pain syndrome (IC/BPS) could be visualized with molecularly-targeted magnetic resonance imaging (mt-MRI) . IC/BPS is a chronic, painful condition of the bladder that affects primarily women. It has been demonstrated over the past several decades that permeability plays a substantial role in IC/BPS. There are several key molecular markers that have been associated with permeability, including glycolsaminoglycan (GAG), biglycan, chondroitin sulfate, decorin, E-cadherin, keratin 20, uroplakin, vascular endothelial growth factor receptor 1 (VEGF-R1), claudin-2 and zonula occludens-1 (ZO-1). We used molecularly-targeted MRI (mt-MRI) to assess specific urothelial biomarkers (decorin, VEGF-R1, and claudin-2) associated with bladder hyper-permeability in a protamine sulfate (PS)-induced rat model. The mt-MRI probes consisted of an antibody against either VEGF-R1, decorin or claudin-2 conjugated to albumin that had also Gd-DTPA (gadolinium diethylene triamine penta acetic acid) and biotin attached. mt-MRI- and histologically-detectable levels of decorin and VEGF-R1 were both found to decrease following PS-induced bladder urothelial hyper-permeability, whereas claudin-2, was found to increase in the rat PS model. Verification of the presence of the mt-MRI probes were done by targeting the biotin moiety for each respective probe with streptavidin-hose radish peroxidase (HRP). Levels of protein expression for VEGF-R1, decorin and claudin-2 were confirmed with immunohistochemistry. molecularly-targeted MRI (mt-MRI) was found to successfully detect alterations in the expression of decorin, VEGFR1 and claudin-2 in a PS-induced rat bladder permeability model. This molecularly-targeted imaging approach has the potential to provide invaluable information to enhance our understanding of bladder urothelium hyper-permeability in IC/BPS patients, and perhaps be used to assist in developing novel therapeutic strategies.
机译:目的是研究是否可以通过分子靶向磁共振成像(mt-MRI)观察与间质性膀胱炎/膀胱疼痛综合征(IC / BPS)相关的膀胱高通透性的一些关键分子因素。 IC / BPS是一种慢性疼痛性膀胱疾病,主要影响女性。在过去的几十年中,已经证明导磁率在IC / BPS中起着重要作用。有几个与渗透性相关的关键分子标记,包括乙二醇氨基聚糖(GAG),双糖链蛋白,硫酸软骨素,核心蛋白,E-钙粘着蛋白,角蛋白20,尿激酶,血管内皮生长因子受体1(VEGF-R1),claudin-2和小带遮挡物1(ZO-1)。我们使用分子靶向MRI(mt-MRI)评估了硫酸鱼精蛋白(PS)诱导的大鼠模型中与膀胱高通透性相关的特定尿路上皮生物标志物(decorin,VEGF-R1和claudin-2)。 mt-MRI探针由针对与白蛋白偶联的VEGF-R1,decorin或claudin-2的抗体组成,该抗体还具有Gd-DTPA(ga二亚乙基三胺五乙酸)和生物素。 mt-MRI和组织学检测到的decorin和VEGF-R1水平在PS诱导的膀胱尿路上皮过度通透性均降低,而claudin-2在大鼠PS模型中升高。通过使用链霉亲和素-软管萝卜过氧化物酶(HRP)靶向每个探针的生物素部分,来验证mt-MRI探针的存在。免疫组织化学证实了VEGF-R1,decorin和claudin-2的蛋白表达水平。发现分子靶向MRI(mt-MRI)可成功检测PS诱导的大鼠膀胱通透性模型中decorin,VEGFR1和claudin-2表达的变化。这种以分子为靶标的成像方法有可能提供宝贵的信息,以增强我们对IC / BPS患者对膀胱尿路上皮过度通透性的了解,并可能有助于开发新的治疗策略。

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