利用分子磁共振成像在小鼠烧伤模型中追踪标记干细胞作为再生医学的一种方法。

Zeba Qadri, Valeria Righi, Shasha Li, A Aria Tzika
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引用次数: 2

摘要

基于干细胞移植的治疗方法在再生医学领域提供了巨大的潜力。及时监测移植干细胞的命运被认为是干细胞移植长期成功的主要限制之一。实时可视化和无创跟踪体内干细胞的成像方法有助于成功的细胞移植技术的发展。新型的非侵入性分子成像方法,特别是MRI,近年来引起了人们的极大兴趣。因此,对具有临床意义的小鼠模型进行了研究,注射造影剂用于标记细胞,如用于细胞成像的超顺磁性氧化铁(SPIO)纳米颗粒。可用于生成正对比图像的MR技术最近与跟踪标记细胞有很大的相关性。特别是当标记细胞附近的非共振区域被选择性地激发,而非标记区域的信号被光谱去相法抑制时。因此,本研究的范围是在烧伤小鼠模型中采用无创方式的体内正对比磁共振成像方法跟踪磁标记细胞。这些结果对在伤口愈合的某个阶段监测标记干细胞具有直接意义。我们建议我们的方法可以用于分子医学和再生医学的临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tracking of Labelled Stem Cells Using Molecular MR Imaging in a Mouse Burn Model <i>in Vivo</i> as an Approach to Regenerative Medicine.

Tracking of Labelled Stem Cells Using Molecular MR Imaging in a Mouse Burn Model <i>in Vivo</i> as an Approach to Regenerative Medicine.

Tracking of Labelled Stem Cells Using Molecular MR Imaging in a Mouse Burn Model <i>in Vivo</i> as an Approach to Regenerative Medicine.

Tracking of Labelled Stem Cells Using Molecular MR Imaging in a Mouse Burn Model in Vivo as an Approach to Regenerative Medicine.

Therapies based on stem cell transplants offer significant potential in the field of regenerative medicine. Monitoring the fate of the transplanted stem cells in a timely manner is considered one of the main limitations for long-standing success of stem cell transplants. Imaging methods that visualize and track stem cells in vivo non-invasively in real time are helpful towards the development of successful cell transplantation techniques. Novel molecular imaging methods which are non-invasive particularly such as MRI have been of great recent interest. Hence, mouse models which are of clinical relevance have been studied by injecting contrast agents used for labelling cells such as super-paramagnetic iron-oxide (SPIO) nanoparticles for cellular imaging. The MR techniques which can be used to generate positive contrast images have been of much relevance recently for tracking of the labelled cells. Particularly when the off-resonance region in the vicinity of the labeled cells is selectively excited while suppressing the signals from the non-labeled regions by the method of spectral dephasing. Thus, tracking of magnetically labelled cells employing positive contrast in vivo MR imaging methods in a burn mouse model in a non-invasive way has been the scope of this study. The consequences have direct implications for monitoring labeled stem cells at some stage in wound healing. We suggest that our approach can be used in clinical trials in molecular and regenerative medicine.

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