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99mTc-Based Imaging of Transplanted Neural Stem Cells and Progenitor Cells

机译:基于99mTc的神经干细胞和祖细胞移植成像

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Cell therapy for neurologic disorders will benefit significantly from progress in methods of noninvasively imaging cell transplants. The success of current cell therapy has varied, in part because of differences in cell sources, differences in transplantation procedures, and lack of understanding of cell fate after transplantation. Standardization of transplantation procedures will progress with noninvasive imaging. In turn, in vivo imaging will enhance our understanding of neural transplant biology and improve therapeutic outcomes. The goal of this study was to determine the effect of a 99mTc-based probe on neural stem and progenitor cell transplants and validate the SPECT images of the transplanted cells. >Methods: We previously developed a method to label neural stem and progenitor cells with 99mTc to visualize these cells in the brain with SPECT. The cells were initially labeled with a permeation peptide carrying a chelate for 99mTc. The proliferation and differentiation characteristics of the labeled cells were studied in tissue culture. In parallel experiments, the labeled cells were stereotactically injected into the rat brain, and the site of transplantation was verified with histochemistry and phosphorimaging. >Results: The accuracy of the transplant location obtained by SPECT was confirmed by comparison with phosphorimages and histologic sections of the brain. The labeling did, however, decrease the proliferative capacity of the neural stem and progenitor cells. >Conclusion: The labeling technique described here can be used to standardize the location of cell transplants in the brain and quantify the number of transplanted cells. However, a 99mTc-based probe can decrease the cellular proliferation of neural progenitor cells.
机译:神经系统疾病的细胞疗法将从无创成像细胞移植方法的进展中显着受益。当前细胞疗法的成功有所不同,部分原因是细胞来源不同,移植程序不同以及移植后对细胞命运的了解不足。无创成像技术将促进移植程序的标准化。反过来,体内成像将增强我们对神经移植生物学的了解并改善治疗效果。这项研究的目的是确定基于 99m Tc的探针对神经干细胞和祖细胞移植的影响,并验证移植细胞的SPECT图像。 >方法:我们以前开发了一种用 99m Tc标记神经干细胞和祖细胞的方法,以便通过SPECT可视化大脑中的这些细胞。最初用标记为 99m Tc的螯合物的渗透肽标记细胞。在组织培养中研究了标记细胞的增殖和分化特征。在平行实验中,将标记的细胞立体定向注入大鼠脑部,并通过组织化学和磷光成像验证了移植部位。 >结果:通过SPECT获得的移植位置的准确度通过与脑部的磷光图像和组织学切片进行比较得到了证实。但是,标记确实降低了神经干细胞和祖细胞的增殖能力。 >结论:这里描述的标记技术可用于标准化细胞移植在大脑中的位置并量化移植的细胞数量。但是,基于 99m Tc的探针可以减少神经祖细胞的细胞增殖。

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