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使用具有钆增强磁共振成像和近红外荧光的双成像探针在体内追踪吞噬性免疫细胞

In Vivo Tracking of Phagocytic Immune Cells Using a Dual Imaging Probe with Gadolinium-Enhanced MRI and Near-Infrared Fluorescence.

作者信息

Kim Eun-Joong, Bhuniya Sankarprasad, Lee Hyunseung, Kim Hyun Min, Shin Weon Sup, Kim Jong Seung, Hong Kwan Soo

机构信息

Bioimaging Research Team, Korea Basic Science Institute , Cheongju 28119, Korea.

Department of Chemistry, Korea University , Seoul 02841, Korea.

出版信息

ACS Appl Mater Interfaces. 2016 Apr 27;8(16):10266-73. doi: 10.1021/acsami.6b03344. Epub 2016 Apr 15.

Abstract

A novel dual imaging probe for in vivo magnetic resonance imaging (MRI) and optical imaging was developed by combining gadolinium (Gd)-chelating MR probe and a near-infrared (NIR) fluorophore, aza-BODIPY (AB; BODIPY = boron-dipyrromethene). This aza-BODIPY-based bimodal contrast agent (AB-BCA) showed a significant fluorescence emission around the NIR range and an enhanced longitudinal relaxivity in MR modality. The probe was easily delivered to phagocytic cells of the innate immune system, together with macrophages and dendritic cells (DCs), and presented high-performance fluorescence and MR imaging without obvious cytotoxicity. For in vivo visualization of AB-BCA using MRI and optical imaging, bone marrow-derived DCs were labeled and injected into the footpad of mice, and labeled DCs were tracked in vivo. We observed the migration of AB-BCA-labeled DCs into the lymph nodes via lymphatic vessels using NIR fluorescence and T1-weighted MR images. This dual-modality imaging probe was used for noninvasive monitoring of DC migration into lymph nodes and could be useful for investigating advanced cellular immunotherapy.

摘要

通过将钆(Gd)螯合磁共振探针与近红外(NIR)荧光团氮杂-BODIPY(AB;BODIPY = 硼二吡咯亚甲基)相结合,开发出了一种用于体内磁共振成像(MRI)和光学成像的新型双成像探针。这种基于氮杂-BODIPY的双模态造影剂(AB-BCA)在近红外范围内显示出显著的荧光发射,并且在磁共振模式下具有增强的纵向弛豫率。该探针能够轻松地递送至先天免疫系统的吞噬细胞,包括巨噬细胞和树突状细胞(DCs),并呈现出高性能的荧光和磁共振成像,且无明显细胞毒性。为了使用MRI和光学成像在体内可视化AB-BCA,对骨髓来源的DCs进行标记并注射到小鼠的足垫中,然后在体内追踪标记的DCs。我们利用近红外荧光和T1加权磁共振图像观察到AB-BCA标记的DCs通过淋巴管迁移至淋巴结。这种双模态成像探针用于对DCs迁移至淋巴结进行无创监测,可能有助于研究先进的细胞免疫疗法。

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