Department of Neurology, University of Miami Miller School of Medicine, Miami, FL, USA.
Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL, USA.
Neurol Res. 2024 Apr;46(4):326-329. doi: 10.1080/01616412.2024.2303879. Epub 2024 Mar 11.
Cell-based therapy has emerged as a promising avenue for post-stroke recovery. A significant challenge lies in tracking the distribution and engraftment of transplanted cells within the target cerebral tissue. To address this, we turn to the potential of Brain MRI detection of mesenchymal stem cells (MSCs), achieved by labeling these cells with superparamagnetic iron oxide (SPIO). This is the first report of a technique to label canine MSCs using a commercially available SPIO, Molday ION Rhodamine B (MIRB), to optimize both viability and labeling efficacy for transplantation purposes."
Canine MSCs were incubated with addition of different MIRB concentration from 0, 10, 20, 30 μg Fe/ml. The cellular uptake of MIRB was confirmed through the analysis of fluorescent images and flow cytometry. The morphological characteristics of MSCs were assessed via microscopic visualization. Cellular viability was evaluated using both a cellometer and flow cytometry.
Fluorescent microscopic images of all MIRB incubated MSCs groups show >70% labeled cells with homogenous signal intensity. Notably, the morphology of MSCs remained unaltered in the 10 μg Fe/ml group compared to the control group. Furthermore, among the labeled groups, the 10 μg Fe/ml concentration exhibited the highest viability when assessed using two different flow cytometry methods (95.3%, < 0.05).
This study successfully labels canine MSCs with MIRB. The optimal concentration of 10 μg Fe/ml demonstrates optimal viability, labeling efficacy, and preserved cellular morphology.
细胞疗法已成为中风后恢复的一种有前途的方法。一个重大的挑战在于追踪移植细胞在目标脑组织内的分布和植入。为了解决这个问题,我们转向了通过超顺磁性氧化铁 (SPIO) 标记间充质干细胞 (MSCs) 来实现大脑 MRI 检测的潜力。这是第一个使用市售 SPIO,即 Molday ION Rhodamine B (MIRB) 标记犬 MSCs 的技术报告,旨在优化细胞活力和标记效率,以满足移植目的。
将犬 MSCs 与不同浓度的 MIRB(0、10、20、30μg Fe/ml)孵育。通过荧光图像和流式细胞术分析确认 MIRB 的细胞摄取。通过显微镜可视化评估 MSCs 的形态特征。使用细胞计数器和流式细胞术评估细胞活力。
所有 MIRB 孵育的 MSCs 组的荧光显微镜图像均显示>70%的标记细胞具有均匀的信号强度。值得注意的是,与对照组相比,10μg Fe/ml 组的 MSCs 形态保持不变。此外,在标记组中,当使用两种不同的流式细胞术方法评估时,10μg Fe/ml 浓度表现出最高的活力(95.3%,<0.05)。
本研究成功地用 MIRB 标记了犬 MSCs。最佳浓度为 10μg Fe/ml 时,具有最佳的活力、标记效率和保留的细胞形态。