Neuroscience Institute, University Miguel Hernandez-Spanish Council for Scientific Research (UMH-CSIC), Alicante, Spain.
Cell Death Dis. 2013 Aug 29;4(8):e779. doi: 10.1038/cddis.2013.304.
Demyelinating disorders such as leukodystrophies and multiple sclerosis are neurodegenerative diseases characterized by the progressive loss of myelin that may lead toward a chronic demyelination of the brain's white matter, impairing normal axonal conduction velocity and ultimately causing neurodegeneration. Current treatments modifying the pathological mechanisms are capable of ameliorating the disease; however, frequently, these therapies are not sufficient to repress the progressive demyelination into a chronic condition and permanent loss of function. To this end, we analyzed the effect that bone marrow-derived mesenchymal stromal cell (BM-MSC) grafts exert in a chronically demyelinated mouse brain. As a result, oligodendrocyte progenitors were recruited surrounding the graft due to the expression of various trophic signals by the grafted MSCs. Although there was no significant reaction in the non-grafted side, in the grafted regions oligodendrocyte progenitors were detected. These progenitors were derived from the nearby tissue as well as from the neurogenic niches, including the subependymal zone and dentate gyrus. Once near the graft site, the cells matured to myelinating oligodendrocytes. Finally, electrophysiological studies demonstrated that axonal conduction velocity was significantly increased in the grafted side of the fimbria. In conclusion, we demonstrate here that in chronic demyelinated white matter, BM-MSC transplantation activates oligodendrocyte progenitors and induces remyelination in the tissue surrounding the stem cell graft.
脱髓鞘疾病,如白质营养不良和多发性硬化症,是神经退行性疾病,其特征是髓鞘的进行性丧失,这可能导致大脑白质的慢性脱髓鞘,损害正常轴突传导速度,并最终导致神经退行性变。目前,能够改变病理机制的治疗方法可以改善疾病;然而,这些治疗方法常常不足以抑制慢性脱髓鞘病变和功能的永久性丧失。为此,我们分析了骨髓间充质基质细胞(BM-MSC)移植对慢性脱髓鞘小鼠大脑的影响。结果表明,由于移植的 MSC 表达了各种营养信号,因此周围有少突胶质前体细胞被募集。尽管在未移植侧没有明显反应,但在移植区域检测到了少突胶质前体细胞。这些祖细胞来源于附近组织和神经发生龛,包括室管膜下区和齿状回。一旦接近移植部位,细胞就会成熟为髓鞘形成的少突胶质细胞。最后,电生理研究表明,纤维束移植侧的轴突传导速度显著增加。总之,我们在这里证明,在慢性脱髓鞘白质中,BM-MSC 移植激活少突胶质前体细胞,并诱导干细胞移植周围组织的髓鞘再生。