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用于转化医学研究的体内细胞成像

In Vivo Cellular Imaging for Translational Medical Research.

作者信息

Arbab Ali S, Janic Branislava, Haller Jodi, Pawelczyk Edyta, Liu Wei, Frank Joseph A

机构信息

Cellular and Molecular Imaging Laboratory, Department of Radiology, Henry Ford Hospital, Detroit, MI.

出版信息

Curr Med Imaging Rev. 2009 Feb 1;5(1):19-38. doi: 10.2174/157340509787354697.

Abstract

Personalized treatment using stem, modified or genetically engineered, cells is becoming a reality in the field of medicine, in which allogenic or autologous cells can be used for treatment and possibly for early diagnosis of diseases. Hematopoietic, stromal and organ specific stem cells are under evaluation for cell-based therapies for cardiac, neurological, autoimmune and other disorders. Cytotoxic or genetically altered T-cells are under clinical trial for the treatment of hematopoietic or other malignant diseases. Before using stem cells in clinical trials, translational research in experimental animal models are essential, with a critical emphasis on developing noninvasive methods for tracking the temporal and spatial homing of these cells to target tissues. Moreover, it is necessary to determine the transplanted cell's engraftment efficiency and functional capability. Various in vivo imaging modalities are in use to track the movement and incorporation of administered cells. Tagging cells with reporter genes, fluorescent dyes or different contrast agents transforms them into cellular probes or imaging agents. Recent reports have shown that magnetically labeled cells can be used as cellular magnetic resonance imaging (MRI) probes, demonstrating the cell trafficking to target tissues. In this review, we will discuss the methods to transform cells into probes for in vivo imaging, along with their advantages and disadvantages as well as the future clinical applicability of cellular imaging method and corresponding imaging modality.

摘要

使用干细胞、经过修饰的细胞或基因工程细胞进行个性化治疗在医学领域正成为现实,在该领域中,同种异体或自体细胞可用于治疗以及可能用于疾病的早期诊断。造血干细胞、基质干细胞和器官特异性干细胞正在接受评估,以用于心脏、神经、自身免疫和其他疾病的细胞疗法。细胞毒性或基因改造的T细胞正在进行治疗造血或其他恶性疾病的临床试验。在临床试验中使用干细胞之前,在实验动物模型中进行转化研究至关重要,重点是开发用于追踪这些细胞向靶组织的时空归巢的非侵入性方法。此外,有必要确定移植细胞的植入效率和功能能力。各种体内成像方式用于追踪给药细胞的运动和掺入。用报告基因、荧光染料或不同的造影剂标记细胞可将它们转化为细胞探针或成像剂。最近的报告表明,磁性标记的细胞可用作细胞磁共振成像(MRI)探针,证明细胞向靶组织的迁移。在这篇综述中,我们将讨论将细胞转化为体内成像探针的方法,以及它们的优缺点以及细胞成像方法和相应成像方式的未来临床适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0dc/2746660/ffbe3537834a/nihms96806f1.jpg

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