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人脂肪来源的间充质基质细胞在6-羟基多巴胺损伤后可急性增加大鼠脑室下区的内源性神经发生。

Human adipose-derived mesenchymal stromal cells increase endogenous neurogenesis in the rat subventricular zone acutely after 6-hydroxydopamine lesioning.

作者信息

Schwerk Anne, Altschüler Jennifer, Roch Manfred, Gossen Manfred, Winter Christine, Berg Jürgen, Kurtz Andreas, Steiner Barbara

机构信息

Department of Neurology, Charité University Medicine, Berlin, Germany.

Berlin-Brandenburg Centre for Regenerative Therapies, Charité University Medicine, Berlin, Germany.

出版信息

Cytotherapy. 2015 Feb;17(2):199-214. doi: 10.1016/j.jcyt.2014.09.005. Epub 2014 Oct 24.

Abstract

BACKGROUND AIMS

In Parkinson's disease (PD), neurogenesis in the subventricular zone (SVZ)-olfactory bulb (OB) axis is affected as the result of the lack of dopaminergic innervations reaching the SVZ. This aberrant network has been related to the hyposmia of PD patients, which is an early diagnostic marker of the disease. Consequently, much interest arose in finding mechanisms to modulate the SVZ-OB axis. Direct modulation of this axis could be achieved by transplantation of mesenchymal stromal cells (MSC), as it has been shown in rat and mouse PD models. However, the neurogenic effect of MSC in PD was thus far only analyzed weeks after transplantation, and little is known about effects immediately after transplantation.

METHODS

We assessed the acute neuroprotective and neurogenic effects of adipose-derived MSC transplanted into the rat substantia nigra in the 6-hydroxydopamine model of PD.

RESULTS

Three days after transplantation, subventricular neurogenesis was significantly increased in MSC-transplanted versus non-transplanted animals. Most MSC were found in the region of the substantia nigra and the surrounding arachnoid mater, expressing S100β and brain-derived neurotrophic factor, whereas some MSC showed an endothelial phenotype and localized around blood vessels.

CONCLUSIONS

The acute neurogenic effects and neurotrophic factor expression of MSC could help to restore the SVZ-OB axis in PD.

摘要

背景目的

在帕金森病(PD)中,由于缺乏到达脑室下区(SVZ)的多巴胺能神经支配,SVZ-嗅球(OB)轴的神经发生受到影响。这种异常网络与PD患者的嗅觉减退有关,而嗅觉减退是该疾病的早期诊断标志物。因此,人们对寻找调节SVZ-OB轴的机制产生了浓厚兴趣。正如在大鼠和小鼠PD模型中所显示的那样,通过间充质基质细胞(MSC)移植可以直接调节该轴。然而,迄今为止,仅在移植数周后分析了MSC在PD中的神经发生作用,而对于移植后立即产生的影响知之甚少。

方法

我们在6-羟基多巴胺诱导的PD大鼠模型中,评估了脂肪源性MSC移植到黑质后的急性神经保护和神经发生作用。

结果

移植后三天,与未移植动物相比,移植MSC的动物脑室下区神经发生显著增加。大多数MSC位于黑质区域和周围的蛛网膜下,表达S100β和脑源性神经营养因子,而一些MSC表现出内皮细胞表型并定位于血管周围。

结论

MSC的急性神经发生作用和神经营养因子表达可能有助于恢复PD中的SVZ-OB轴。

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