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兔急性周围神经牵拉损伤模型中转基因间充质干细胞的体内 MRI 示踪研究。

In vivo MR imaging tracking of transplanted mesenchymal stem cells in a rabbit model of acute peripheral nerve traction injury.

机构信息

Department of Radiology, The Second Affiliated Hospital, Sun Yat-Sen University, Guangzhou, Guangdong, China. junshenjun@ hotmail.com

出版信息

J Magn Reson Imaging. 2010 Nov;32(5):1076-85. doi: 10.1002/jmri.22353.

DOI:10.1002/jmri.22353
PMID:21031511
Abstract

PURPOSE

To investigate in vivo MRI tracking mesenchymal stem cells (MSCs) in peripheral nerve injures using a clinically available paramagnetic contrast agent (Gd-DTPA) and commercially available rhodamine-incorporated transfection reagents (PEI-FluoR).

MATERIALS AND METHODS

After bone marrow MSCs were labeled with Gd-DTPA and PEI-FluoR complex, the labeling efficacy and longevity of Gd-DTPA maintenance were measured and cell viability, proliferation, and apoptosis were assessed. Thirty-six rabbits with acute sciatic nerve traction injury randomly received 1 × 10(6) labeled (n = 12) or unlabeled MSCs (n = 12) or vehicle alone injection. The distribution and migration of implanted cells was followed by MRI and correlated with histology. The relative signal intensity (RSL) of the grafts was measured.

RESULTS

The labeling efficiency was 76 ± 4.7% and the labeling procedure did not influence cell viability, proliferation, and apoptosis. A persistent higher RSL in grafts was found in the labeled group compared with the unlabeled and vehicle groups until 10 days after transplantation (P < 0.05). The distribution and migration of labeled cells could be tracked by MRI until 10 days after transplantation. Transplanted MSCs were not found to transdifferentiate into Schwann-like cells within 14-day follow-up.

CONCLUSION

Labeling MSCs with the dual agents may enable cellular MRI of the engraftment in the experimental peripheral nerve injury.

摘要

目的

使用临床可用的顺磁对比剂(Gd-DTPA)和市售的罗丹明掺入转染试剂(PEI-FluoR),在周围神经损伤中体内 MRI 追踪间充质干细胞(MSCs)。

材料和方法

将 Gd-DTPA 和 PEI-FluoR 复合物标记骨髓间充质干细胞后,测量 Gd-DTPA 维持的标记效率和持久性,并评估细胞活力、增殖和凋亡。36 只急性坐骨神经牵引损伤兔随机接受 1×10(6)标记(n = 12)或未标记(n = 12)MSCs 或单独载体注射。通过 MRI 跟踪植入细胞的分布和迁移,并与组织学相关联。测量移植物的相对信号强度(RSL)。

结果

标记效率为 76±4.7%,标记过程不影响细胞活力、增殖和凋亡。与未标记和载体组相比,标记组在移植后 10 天内发现移植物的 RSL 持续升高(P<0.05)。标记细胞的分布和迁移可以通过 MRI 追踪到移植后 10 天。在 14 天的随访中,未发现移植的 MSCs 向雪旺样细胞转分化。

结论

用双试剂标记 MSCs 可能使实验性周围神经损伤中的植入物的细胞 MRI 成为可能。

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