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磁共振成像追踪用葡聚糖颗粒标记的巨噬细胞,这些颗粒内包裹着一种不溶于水的顺磁性镧系元素基造影剂。

MRI tracking of macrophages labeled with glucan particles entrapping a water insoluble paramagnetic Gd-based agent.

机构信息

Department of Molecular Biotechnology and Health Sciences and Molecular and Preclinical Imaging Centers, University of Turin, Turin, Italy.

出版信息

Mol Imaging Biol. 2013 Jun;15(3):307-15. doi: 10.1007/s11307-012-0603-x.

Abstract

PURPOSE

This study is aimed at demonstrating the in vivo potential of Gd(III)-loaded glucan particles (Gd-GPs) as magnetic resonance imaging (MRI)-positive agents for labeling and tracking phagocytic cells.

PROCEDURE

GPs were obtained from Saccharomyces cerevisae and loaded with the water-insoluble complex Gd-DOTAMA(C18)2. The uptake kinetics of Gd-GPs by murine macrophages was studied in vitro and the internalization mechanism was assessed by competition assays. The in vivo performance of Gd-GPs was tested at 7.05 T on a mouse model of acute liver inflammation.

RESULTS

The minimum number of Gd-GPs-labeled J774.A1 macrophages detected in vitro by MRI was ca. 300 cells/μl of agar, which is the lowest number ever reported for cells labeled with a positive T1 agent. Intravenous injection of macrophages labeled with Gd-GPs in a mouse model of liver inflammation enabled the MRI visualization of the cellular infiltration in the diseased area.

CONCLUSIONS

Gd-GPs represent a promising platform for tracking macrophages by MRI as a T1 alternative to the golden standard T2-based iron oxide particles.

摘要

目的

本研究旨在证明负载钆(III)的葡聚糖颗粒(Gd-GPs)作为磁共振成像(MRI)阳性造影剂用于标记和跟踪吞噬细胞的体内潜力。

过程

GPs 从酿酒酵母中获得,并负载水不溶性配合物 Gd-DOTAMA(C18)2。研究了 Gd-GPs 被小鼠巨噬细胞体外摄取的动力学,并通过竞争实验评估了内化机制。在 7.05T 下,在急性肝炎症的小鼠模型上测试了 Gd-GPs 的体内性能。

结果

通过 MRI 体外检测到的最低数量的 Gd-GPs 标记的 J774.A1 巨噬细胞约为 300 个细胞/μl 琼脂,这是迄今为止用阳性 T1 造影剂标记的细胞报道的最低数量。在肝炎症的小鼠模型中静脉注射 Gd-GPs 标记的巨噬细胞,使病变区域的细胞浸润能够通过 MRI 可视化。

结论

Gd-GPs 代表了一种通过 MRI 跟踪巨噬细胞的有前途的平台,可作为替代金标准基于 T2 的氧化铁颗粒的 T1 造影剂。

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