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背根神经节神经元诱导间充质干细胞沿雪旺细胞谱系发生转分化。

Dorsal root ganglion neurons induce transdifferentiation of mesenchymal stem cells along a Schwann cell lineage.

作者信息

Yang Jinsong, Lou Qiang, Huang Renzheng, Shen Longxiang, Chen Zhengrong

机构信息

Department of Orthopaedics, Zhongshan Hospital, Fudan University, Shanghai 200032, PR China.

出版信息

Neurosci Lett. 2008 Nov 21;445(3):246-51. doi: 10.1016/j.neulet.2008.09.015. Epub 2008 Sep 11.

Abstract

It has been reported that mesenchymal stem cells (MSCs) can transdifferentiate into Schwann cell-like cells by a series of treatments with a reducing agent, retinoic acid and a combination of trophic factors in vitro, and can transdifferentiate into myelin-forming cells to repair the demyelinated rat spinal cord in vivo. We now report that when co-cultured with dorsal root ganglion (DRG) neurons, MSCs were induced to transdifferentiate into Schwann cell-like cells that had ensheathed DRG axons. Following differentiation, MSCs underwent morphological changes similar to those of cultured Schwann cells and express GFAP and S100, the marker of Schwann cells. Moreover, 6 weeks later, MSCs wrapped their membrane around DRG axons. Further, initiation of myelination was observed in the co-cultured DRG neurons, which was determined by signals to MBP and this initiation of axon myelination by MSCs is similar to that of Schwann cells. However, electron micrographs show that no compact myelin was present in the MSCs co-cultures, whereas the Schwann cells co-cultures had formed a multilammelar myelin sheath around the axon. These indicate that the release of cytokine by DRG neurons may promote the transdifferentiation of MSCs, but is not sufficient to elicit compact myelination by transdifferentiated MSCs. These results improve our understanding in the mechanism of MSC transdifferentiation, and the mechanism underlying ensheathment and myelination by transdifferentiated MSCs.

摘要

据报道,间充质干细胞(MSCs)在体外经还原剂、视黄酸和多种营养因子联合处理后可转分化为雪旺氏细胞样细胞,并在体内可转分化为形成髓鞘的细胞以修复脱髓鞘的大鼠脊髓。我们现在报道,当与背根神经节(DRG)神经元共培养时,MSCs被诱导转分化为包裹DRG轴突的雪旺氏细胞样细胞。分化后,MSCs发生了与培养的雪旺氏细胞相似的形态变化,并表达雪旺氏细胞的标志物GFAP和S100。此外,6周后,MSCs将其细胞膜包裹在DRG轴突周围。此外,在共培养的DRG神经元中观察到髓鞘形成的起始,这是由MBP信号决定的,并且MSCs引发的轴突髓鞘形成与雪旺氏细胞相似。然而,电子显微镜照片显示,在MSCs共培养物中不存在紧密髓鞘,而雪旺氏细胞共培养物在轴突周围形成了多层髓鞘。这些表明DRG神经元释放的细胞因子可能促进MSCs的转分化,但不足以引发转分化的MSCs形成紧密髓鞘。这些结果增进了我们对MSCs转分化机制以及转分化的MSCs形成髓鞘和包裹轴突的潜在机制的理解。

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