BioImaging Laboratory, University of Antwerp, Antwerp, Belgium.
Mol Imaging Biol. 2011 Dec;13(6):1133-45. doi: 10.1007/s11307-011-0469-3.
Development of multimodal imaging strategies is currently of utmost importance for the validation of preclinical stem cell therapy studies.
We performed a combined labeling strategy for bone marrow-derived stromal cells (BMSC) based on genetic modification with the reporter genes Luciferase and eGFP (BMSC-Luc/eGFP) and physical labeling with blue fluorescent micron-sized iron oxide particles (MPIO) in order to unambiguously identify BMSC localization, survival, and differentiation following engraftment in the central nervous system of mice by in vivo bioluminescence (BLI) and magnetic resonance imaging and postmortem histological analysis.
Using this combination, a significant increase of in vivo BLI signal was observed for MPIO-labeled BMSC-Luc/eGFP. Moreover, MPIO labeling of BMSC-Luc/eGFP allows for the improved identification of implanted cells within host tissue during histological observation.
This study describes an optimized labeling strategy for multimodal stem cell imaging resulting in improved quantitative and qualitative detection of cellular grafts.
开发多模态成像策略对于验证临床前干细胞治疗研究至关重要。
我们采用联合标记策略对骨髓基质细胞(BMSC)进行标记,该策略基于报告基因荧光素酶和增强型绿色荧光蛋白(BMSC-Luc/eGFP)的遗传修饰,以及蓝色荧光微米级氧化铁颗粒(MPIO)的物理标记,以便通过活体生物发光(BLI)和磁共振成像以及死后组织学分析,在小鼠中枢神经系统中明确识别植入后的 BMSC 定位、存活和分化。
使用这种组合,MPIO 标记的 BMSC-Luc/eGFP 的体内 BLI 信号显著增加。此外,MPIO 标记的 BMSC-Luc/eGFP 允许在组织学观察期间改善对宿主组织内植入细胞的识别。
本研究描述了一种优化的多模态干细胞成像标记策略,可提高细胞移植物的定量和定性检测。