Torres Ana Luiza Machado, Jelicks Linda, de Carvalho Antonio Carlos Campos, Spray David C, Mendez-Otero Rosalia
Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Methods Mol Biol. 2012;906:239-52. doi: 10.1007/978-1-61779-953-2_18.
Stem cell therapy has emerged as a potential therapeutic option for cell death-related heart diseases. Application of non-invasive cell tracking approaches is necessary to determine tissue distribution and lifetime of stem cells following their injection and will likely provide knowledge about poorly understood stem cells mechanisms of tissue repair. Magnetic resonance imaging (MRI) is a potentially excellent tool for high-resolution visualization of the fate of cells after transplantation and for evaluation of therapeutic strategies. The application of MRI for in vivo cell tracking requires contrast agents to achieve efficient cell labeling without causing any toxic cellular effects or eliciting any other side effects. For these reasons clinically approved contrast agents (e.g., ferumoxides) and incorporation facilitators (e.g., protamine) are currently the preferred materials for cell labeling and tracking. Here we describe how to use superparamagnetic iron oxide nanoparticles to label cells and to monitor cell fate in several disease models.
干细胞疗法已成为治疗与细胞死亡相关的心脏病的一种潜在治疗选择。应用非侵入性细胞追踪方法对于确定干细胞注射后的组织分布和存活时间是必要的,并且可能会提供有关目前了解甚少的干细胞组织修复机制的知识。磁共振成像(MRI)是用于高分辨率可视化移植后细胞命运和评估治疗策略的潜在优秀工具。将MRI应用于体内细胞追踪需要造影剂以实现有效的细胞标记,而不会引起任何细胞毒性作用或引发任何其他副作用。由于这些原因,目前临床批准的造影剂(例如,超顺磁性氧化铁)和掺入促进剂(例如,鱼精蛋白)是细胞标记和追踪的首选材料。在此,我们描述了如何使用超顺磁性氧化铁纳米颗粒标记细胞并在几种疾病模型中监测细胞命运。