Wellcome Trust and MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB20AH, UK.
Institute of Molecular Regenerative Medicine, Paracelsus Medical University Salzburg, 5020 Salzburg, Austria; Spinal Cord Injury and Tissue Regeneration Center Salzburg (SCI-TReCS), Paracelsus Medical University Salzburg, 5020 Salzburg, Austria.
Cell Rep. 2017 Aug 22;20(8):1755-1764. doi: 10.1016/j.celrep.2017.08.007.
The role of the neurovascular niche in CNS myelin regeneration is incompletely understood. Here, we show that, upon demyelination, CNS-resident pericytes (PCs) proliferate, and parenchymal non-vessel-associated PC-like cells (PLCs) rapidly develop. During remyelination, mature oligodendrocytes were found in close proximity to PCs. In Pdgfb mice, which have reduced PC numbers, oligodendrocyte progenitor cell (OPC) differentiation was delayed, although remyelination proceeded to completion. PC-conditioned medium accelerated and enhanced OPC differentiation in vitro and increased the rate of remyelination in an ex vivo cerebellar slice model of demyelination. We identified Lama2 as a PC-derived factor that promotes OPC differentiation. Thus, the functional role of PCs is not restricted to vascular homeostasis but includes the modulation of adult CNS progenitor cells involved in regeneration.
神经血管龛在中枢神经系统髓鞘再生中的作用尚未完全阐明。在这里,我们发现,在脱髓鞘后,中枢神经系统驻留的周细胞(PCs)增殖,实质非血管相关的 PC 样细胞(PLCs)迅速发育。在髓鞘再生过程中,成熟的少突胶质细胞被发现与 PCs 紧密相邻。在 Pdgfb 小鼠中,PC 数量减少,少突胶质前体细胞(OPC)分化延迟,尽管髓鞘再生仍能完成。PC 条件培养基在体外加速和增强 OPC 分化,并增加脱髓鞘小脑切片模型中髓鞘再生的速度。我们确定 Lama2 是一种促进 OPC 分化的 PC 衍生因子。因此,PC 的功能作用不仅限于血管稳态,还包括调节参与再生的成年中枢神经系统祖细胞。