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首页> 外文期刊>BMC Neuroscience >Nestin-positive mesenchymal stem cells favour the astroglial lineage in neural progenitors and stem cells by releasing active BMP4
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Nestin-positive mesenchymal stem cells favour the astroglial lineage in neural progenitors and stem cells by releasing active BMP4

机译:Nestin阳性间充质干细胞通过释放活性BMP4促进神经祖细胞和干细胞的星形胶质谱系

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Background Spontaneous repair is limited after CNS injury or degeneration because neurogenesis and axonal regrowth rarely occur in the adult brain. As a result, cell transplantation has raised much interest as potential treatment for patients with CNS lesions. Several types of cells have been considered as candidates for such cell transplantation and replacement therapies. Foetal brain tissue has already been shown to have significant effects in patients with Parkinson's disease. Clinical use of the foetal brain tissue is, however, limited by ethical and technical problems as it requires high numbers of grafted foetal cells and immunosuppression. Alternatively, several reports suggested that mesenchymal stem cells, isolated from adult bone marrow, are multipotent cells and could be used in autograft approach for replacement therapies. Results In this study, we addressed the question of the possible influence of mesenchymal stem cells on neural stem cell fate. We have previously reported that adult rat mesenchymal stem cells are able to express nestin in defined culture conditions (in the absence of serum and after 25 cell population doublings) and we report here that nestin-positive (but not nestin-negative) mesenchymal stem cells are able to favour the astroglial lineage in neural progenitors and stem cells cultivated from embryonic striatum. The increase of the number of GFAP-positive cells is associated with a significant decrease of the number of Tuj1- and O4-positive cells. Using quantitative RT-PCR, we demonstrate that mesenchymal stem cells express LIF, CNTF, BMP2 and BMP4 mRNAs, four cytokines known to play a role in astroglial fate decision. In this model, BMP4 is responsible for the astroglial stimulation and oligodendroglial inhibition, as 1) this cytokine is present in a biologically-active form only in nestin-positive mesenchymal stem cells conditioned medium and 2) anti-BMP4 antibodies inhibit the nestin-positive mesenchymal stem cells conditioned medium inducing effect on astrogliogenesis. Conclusions When thinking carefully about mesenchymal stem cells as candidates for cellular therapy in neurological diseases, their effects on resident neural cell fate have to be considered.
机译:背景技术中枢神经系统损伤或变性后,自发修复受到限制,因为在成年大脑中很少发生神经发生和轴突再生。结果,细胞移植作为中枢神经系统病变患者的潜在治疗引起了广泛的兴趣。已经考虑了几种类型的细胞作为这种细胞移植和替代疗法的候选者。胎儿脑组织已经显示出对帕金森氏病患者有显著作用。然而,由于需要大量移植的胎儿细胞和免疫抑制作用,因此胎儿脑组织的临床使用受到伦理和技术问题的限制。另外,一些报道表明,从成年骨髓中分离的间充质干细胞是多能细胞,可用于自体移植方法以替代疗法。结果在这项研究中,我们解决了间充质干细胞对神经干细胞命运的可能影响的问题。我们以前曾报道过成年大鼠间充质干细胞能够在规定的培养条件下(在无血清的情况下和25个细胞群加倍后)表达巢蛋白,在此我们报道巢蛋白阳性(但巢蛋白阴性的)间充质干细胞能够支持从胚胎纹状体培养的神经祖细胞和干细胞中的星形胶质细胞系。 GFAP阳性细胞数目的增加与Tuj1和O4阳性细胞数目的显着减少有关。使用定量RT-PCR,我们证明间充质干细胞表达LIF,CNTF,BMP2和BMP4 mRNA,这四种细胞因子已知在星形胶质命运决定中发挥作用。在该模型中,BMP4负责星形胶质细胞的刺激和少突胶质细胞的抑制,因为1)这种细胞因子仅以巢蛋白阳性的间充质干细胞条件培养基为生物活性形式存在,并且2)抗BMP4抗体抑制巢蛋白阳性间充质干细胞条件培养基对星形胶质细胞发生的诱导作用。结论当仔细考虑间充质干细胞作为神经系统疾病细胞治疗的候选者时,必须考虑它们对固有神经细胞命运的影响。

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