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间充质干细胞和局部他克莫司递呈协同促进轴突延伸。

Mesenchymal stem cells and local tacrolimus delivery synergistically enhance neurite extension.

机构信息

Division of Hand and Microvascular Surgery, Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.

Department of Plastic-, Reconstructive- and Hand Surgery, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, The Netherlands.

出版信息

Biotechnol Bioeng. 2021 Nov;118(11):4477-4487. doi: 10.1002/bit.27916. Epub 2021 Aug 25.

Abstract

BACKGROUND

The aim of this study was to investigate the combined effect of mesenchymal stem cells (MSC) and local delivery of tacrolimus (FK506) on nerve regeneration when applied to nerve autografts and decellularized allografts.

METHODS

A three-dimensional in vitro compartmented cell culture system consisting of a neonatal dorsal root ganglion adjacent to a nerve graft was used to evaluate the regenerating neurites into the peripheral nerve scaffold. Nerve autografts and allografts were treated with (i) undifferentiated MSCs, (ii) FK506 (100 ng/mL) or (iii) both (N = 9/group). After 48 hours, neurite extension was measured to quantify nerve regeneration and stem cell viability was evaluated.

RESULTS

Stem cell viability was confirmed in all MSC-treated grafts. Neurite extension was superior in autografts treated with FK506, and MSCs and FK506 combined (p < 0.001 and p = 0.0001, respectively), and autografts treated with MSCs (p = 0.12) were comparable to untreated autografts. In allografts, FK506 treatment and combined treatment were superior to controls (p < 0.001 and p = 0.0001, respectively), and treatment with MSCs (p = 0.09) was comparable to controls. All autograft groups were superior compared to their respective allograft treatment group (p < 0.05) in neurite extension.

CONCLUSIONS

Alone, either MSC or FK506 treatment improved neurite outgrowth, and combined they further enhanced neurite extension in both autografts and allografts.

摘要

背景

本研究旨在探讨间充质干细胞(MSC)与他克莫司(FK506)局部递送至神经自体移植物和去细胞同种异体移植物时对神经再生的联合作用。

方法

使用包含邻近背根神经节的新生儿三维体外分隔细胞培养系统,评估再生神经突进入外周神经支架的情况。神经自体移植物和同种异体移植物分别用(i)未分化 MSC、(ii)FK506(100ng/mL)或(iii)两者处理(每组 N=9)。48 小时后,测量神经突延伸以量化神经再生,评估干细胞活力。

结果

所有 MSC 处理的移植物中均证实了干细胞活力。FK506 处理的自体移植物神经突延伸更好,MSC 和 FK506 联合处理(p<0.001 和 p=0.0001),以及 MSC 处理的自体移植物(p=0.12)与未经处理的自体移植物相当。在同种异体移植物中,FK506 处理和联合处理均优于对照组(p<0.001 和 p=0.0001),MSC 处理与对照组相当(p=0.09)。与各自的同种异体移植物处理组相比,所有自体移植物组的神经突延伸均更好(p<0.05)。

结论

单独使用 MSC 或 FK506 处理均可改善神经突生长,联合使用可进一步增强自体移植物和同种异体移植物的神经突延伸。

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