邓宇斌,毕小彬,沈君,甘丹卉,刘宇,叶美红.Gd-DTPA标记骨髓间质干细胞在脊髓损伤模型中的磁共振示踪研究[J].中国医学影像技术,2008,24(6):843~847
Gd-DTPA标记骨髓间质干细胞在脊髓损伤模型中的磁共振示踪研究
Tracking of mesenchymal stem cells labeled with Gd-DTPA by MR imaging in spinal cord injury model
投稿时间:2008-01-08  修订日期:2008-04-16
DOI:
中文关键词:  细胞标记  骨髓间质干细胞    磁共振成像
英文关键词:Cell labeling  Mesenchymal stem cells  Gd  Magnetic resonance imaging
基金项目:本课题受广东省科技计划项目(2005B50301012)、广东省自然科学基金项目(04300241)资助。
作者单位E-mail
邓宇斌 中山大学中山医学院病理生理教研室,广东 广州 510080 dengyub@mail.sysu.edu.cn 
毕小彬 中山大学中山医学院病理生理教研室,广东 广州 510080  
沈君 中山大学附属第二医院放射科,广东 广州 510120  
甘丹卉 中山大学中山医学院病理生理教研室,广东 广州 510080  
刘宇 中山大学中山医学院病理生理教研室,广东 广州 510080  
叶美红 中山大学中山医学院病理生理教研室,广东 广州 510080  
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中文摘要:
      目的 探讨用钆-二乙烯三胺五乙酸(Gd-DTPA)标记大鼠骨髓间质干细胞(MSCs)用于细胞示踪的可行性。方法 用jetPEITM-FluoF 结合Gd-DTPA形成顺磁性颗粒,标记MSCs,电镜观察标记情况,并用MTT法测定标记细胞的活力。对标记的细胞进行体外和大鼠脊髓内磁共振成像(MRI)。结果 Gd-DTPA可高效标记MSCs,同时对MSCs生长无影响。体外及MSCs移植大鼠脊髓损伤模型MRI T1WI均显示,标记细胞呈高信号强度。结论 Gd-DTPA 成功标记的MSCs在体外和大鼠脊髓组织内均可检测到明显的MRI信号强度改变。Gd-DTPA可以用于MSCs标记的MRI示踪。
英文摘要:
      Objective The aim of the study was to explore the possibility of the rat Mesenchymal stem cells (MSCs) labeled with Gadolinium diethylenetriaminepentaacetic acid (Gd-DTPA) for cell tracking. Methods jetPEITM-FluoF, a cationic polymer transfection reagent, conjugated with Gd-DTPA to form magnetic particles, was used to label MSCs. Electron microscopy was performed to detect the distribution of Gd-DTPA particles in MSCs, and labeling efficiency of Gd-DTPA particles on MSCs was evaluated using immunofluorescence. Viability and proliferation of labeled MSCs were evaluated using MTT assay. Apoptosis of labeled MSCs were evaluated using Hochest 33342 staining. Labeled MSCs was detected with T1-weighed MR imaging in vitro and in rat spinal cord. Results Transmission electron microscopy confirmed the presence of Gd-DTPA particles inside the cells. Labeling efficiency was approximately no less than 80%. MTT values of light absorption were 0.1594±0.0084 for labeled MSCs and 0.1675±0.0063 for unlabelled MSCs after 24 hours post labeling, which had no significant difference (P>0.05). Hochest 33342 staining showed that labeling did not influence the apoptosis of MSCs. Labeled MSCs demonstrated a significant increase signal intensity on T1-weighed MRI in vitro, and the signal intensity of labeled MSCs increased by 26.61% compared with the around spinal cord tissues (P<0.05). Conclusion Rat MSCs could be labeled with Gd-DTPA particles without change the cell viability, proliferation and apoptosis. Obviously labeled MSCs can be imaged in vitro and in vivo in rat spinal cord tissues. Gd-DTPA shows no evident adverse effect on the function of labeled MSCs. Gd-DTPA can be used for the MR imaging tracking of labeled MSCs.
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