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用铁颗粒标记用于磁共振成像的胰岛的活力。

Vitality of pancreatic islets labeled for magnetic resonance imaging with iron particles.

作者信息

Berkova Z, Kriz J, Girman P, Zacharovova K, Koblas T, Dovolilova E, Saudek F

机构信息

Laboratory of Pancreatic Islets, Institute for Clinical and Experimental Medicine, Center for Cell Therapy and Tissue Repair, Videnska 1958/9, 140-21 Prague, Czech Republic.

出版信息

Transplant Proc. 2005 Oct;37(8):3496-8. doi: 10.1016/j.transproceed.2005.09.052.

Abstract

We previously described an in vivo method for pancreatic islet visualization using magnetic resonance imaging with the aid of superparamagnetic nanoparticles of iron oxide (Resovist) or by magnetic beads precoated with antibodies (Dynabeads). The aim of this study was to investigate the in vitro effect of islet labeling on their quality. Isolated rat islets were cultivated for 48 hours with a contrast agent or, in the case of magnetic antibody-coated beads, for only 2 hours. The ability to secrete insulin was tested by a static insulin release assay and the results were expressed as a stimulation index. Staining with propidium iodide and acridine orange was performed to determine the ratio of live to dead cells. Stimulation indices in the Resovist islets (n = 23) vs controls (n = 14) were 15.3 and 15.0, respectively, and in the Dynabeads islets (n = 15) vs controls (n = 12) 21.3 and 19.9, respectively. The vitality of the Resovist islets vs controls determined by live/dead cells ratio was 90.8% and 91.1%, respectively (n = 20), and in the Dynabeads islets vs controls was 89.4% and 91.8%, respectively (n = 11). Islet labeling with the contrast agent as well as with specific antibodies with iron beads did not change the vitality and insulin-secreting capacity assessed in vitro (P > .05). Magnetic resonance using iron nanoparticles represents the only method for in-vivo visualization of transplanted islets so far. Our data represent an important contribution for its clinical use.

摘要

我们之前描述了一种体内胰岛可视化方法,该方法借助超顺磁性氧化铁纳米颗粒(Resovist)或预涂有抗体的磁珠(Dynabeads)通过磁共振成像来实现。本研究的目的是探讨胰岛标记对其质量的体外影响。将分离的大鼠胰岛与造影剂培养48小时,对于磁抗体包被的磁珠,培养仅2小时。通过静态胰岛素释放试验测试胰岛素分泌能力,结果以刺激指数表示。用碘化丙啶和吖啶橙染色以确定活细胞与死细胞的比例。Resovist组胰岛(n = 23)与对照组(n = 14)的刺激指数分别为15.3和15.0,Dynabeads组胰岛(n = 15)与对照组(n = 12)的刺激指数分别为21.3和19.9。通过活/死细胞比例确定的Resovist组胰岛与对照组的活力分别为90.8%和91.1%(n = 20),Dynabeads组胰岛与对照组的活力分别为89.4%和91.8%(n = 11)。用造影剂以及用含铁珠的特异性抗体对胰岛进行标记,并未改变体外评估的活力和胰岛素分泌能力(P > .05)。使用铁纳米颗粒的磁共振成像代表了迄今为止体内可视化移植胰岛的唯一方法。我们的数据对其临床应用具有重要贡献。

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