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间充质干细胞条件培养基对1型脊髓小脑共济失调基因敲入小鼠外周神经元变性的形态学和功能衰减作用

Morphological and Functional Attenuation of Degeneration of Peripheral Neurons by Mesenchymal Stem Cell-Conditioned Medium in Spinocerebellar Ataxia Type 1-Knock-in Mice.

作者信息

Suto Nana, Mieda Tokue, Iizuka Akira, Nakamura Kazuhiro, Hirai Hirokazu

机构信息

Department of Neurophysiology & Neural Repair, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.

Department of Orthopedic Surgery, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.

出版信息

CNS Neurosci Ther. 2016 Aug;22(8):670-6. doi: 10.1111/cns.12560. Epub 2016 May 3.

Abstract

AIMS

Spinocerebellar ataxia type 1 (SCA1) is caused by the ataxin-1 protein (ATXN1) with an abnormally expanded polyglutamine tract and is characterized by progressive neurodegeneration. We previously showed that intrathecal injection of mesenchymal stem cells (MSCs) during the nonsymptomatic stage mitigates the degeneration of the peripheral nervous system (PNS) neurons in SCA1-knock-in (SCA1-KI) mice. We tested in this study whether the therapeutic effects of MSCs in SCA1-KI mice could be reproduced with MSC-releasing factor(s).

METHODS

To test the effects of MSC-releasing factor(s), we used MSC-conditioned medium (MSC-CM). MSC-CM was intrathecally and/or intravenously injected into young SCA1-KI mice, and the therapeutic effects were assessed in the PNS at later ages using immunostaining, electrophysiology, and behavioral tests.

RESULTS

MSC-CM attenuated the degeneration of axons and myelin of spinal motor neurons. Consequently, the injected SCA1-KI mice exhibited smaller reductions in nerve conduction velocity in spinal motor neurons and reduced motor incoordination than the untreated mice.

CONCLUSIONS

These results suggest that factors released from MSC mitigate the morphological and functional abnormalities in the PNS that are observed in SCA1-KI mice in a paracrine manner.

摘要

目的

1型脊髓小脑共济失调(SCA1)由ataxin-1蛋白(ATXN1)引起,其多聚谷氨酰胺序列异常扩增,以进行性神经退行性病变为特征。我们之前表明,在无症状阶段鞘内注射间充质干细胞(MSC)可减轻SCA1基因敲入(SCA1-KI)小鼠外周神经系统(PNS)神经元的退变。在本研究中,我们测试了MSC释放因子是否能重现MSC对SCA1-KI小鼠的治疗效果。

方法

为了测试MSC释放因子的作用,我们使用了MSC条件培养基(MSC-CM)。将MSC-CM鞘内和/或静脉注射到年轻的SCA1-KI小鼠体内,并在后期使用免疫染色、电生理学和行为测试评估PNS中的治疗效果。

结果

MSC-CM减轻了脊髓运动神经元轴突和髓鞘的退变。因此,与未治疗的小鼠相比,注射了MSC-CM的SCA1-KI小鼠脊髓运动神经元的神经传导速度降低幅度较小,运动不协调程度减轻。

结论

这些结果表明,MSC释放的因子以旁分泌方式减轻了SCA1-KI小鼠PNS中观察到的形态和功能异常。

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