Shih Yuda, Ly Philip T T, Wang Jing, Pallen Catherine J
Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
International Collaboration on Repair Discoveries, University of British Columbia, Vancouver, BC, Canada.
J Mol Neurosci. 2017 Aug;62(3-4):329-343. doi: 10.1007/s12031-017-0941-x. Epub 2017 Jun 24.
CNS myelination defects occur in mice deficient in receptor-like protein tyrosine phosphatase alpha (PTPα). Here, we investigated the role of PTPα in oligodendrocyte differentiation and myelination using cells and tissues from wild-type (WT) and PTPα knockout (KO) mice. PTPα promoted the timely differentiation of neural stem cell-derived oligodendrocyte progenitor cells (OPCs). Compared to WT OPCs, KO OPC cultures had more NG2+ progenitors, fewer myelin basic protein (MBP)+ oligodendrocytes, and reduced morphological complexity. In longer co-cultures with WT neurons, more KO than WT OPCs remained NG2+ and while equivalent MBP+ populations of WT and KO cells formed, the reduced area occupied by the MBP+ KO cells suggested that their morphological maturation was impeded. These defects were associated with reduced myelin formation in KO OPC/WT neuron co-cultures. Myelin formation was also impaired when WT OPCs were co-cultured with KO neurons, revealing a novel role for neuronal PTPα in myelination. Canonical Wnt/β-catenin signaling is an important regulator of OPC differentiation and myelination. Wnt signaling activity was not dysregulated in OPCs lacking PTPα, but suppression of Wnt signaling by the small molecule XAV939 remediated defects in KO oligodendrocyte differentiation and enhanced myelin formation by KO oligodendrocytes. However, the myelin segments that formed were significantly shorter than those produced by WT oligodendrocytes, raising the possibility of a role for glial PTPα in myelin extension distinct from its pro-differentiating actions. Altogether, this study reveals PTPα as a molecular coordinator of oligodendroglial and neuronal signals that controls multiple aspects of oligodendrocyte development and myelination.
在缺乏受体样蛋白酪氨酸磷酸酶α(PTPα)的小鼠中会出现中枢神经系统髓鞘形成缺陷。在此,我们使用来自野生型(WT)和PTPα基因敲除(KO)小鼠的细胞和组织,研究了PTPα在少突胶质细胞分化和髓鞘形成中的作用。PTPα促进了神经干细胞来源的少突胶质前体细胞(OPC)的及时分化。与野生型OPC相比,基因敲除OPC培养物中有更多的NG2 +祖细胞、更少的髓鞘碱性蛋白(MBP)+少突胶质细胞,并且形态复杂性降低。在与野生型神经元的较长时间共培养中,基因敲除的OPC中保持NG2 +的比野生型更多,并且虽然野生型和基因敲除细胞形成的MBP +群体相当,但基因敲除的MBP +细胞所占面积减少,表明其形态成熟受到阻碍。这些缺陷与基因敲除的OPC/野生型神经元共培养物中髓鞘形成减少有关。当野生型OPC与基因敲除神经元共培养时,髓鞘形成也受到损害,揭示了神经元PTPα在髓鞘形成中的新作用。经典的Wnt/β-连环蛋白信号传导是OPC分化和髓鞘形成的重要调节因子。在缺乏PTPα的OPC中,Wnt信号活性没有失调,但小分子XAV939对Wnt信号的抑制纠正了基因敲除少突胶质细胞分化中的缺陷,并增强了基因敲除少突胶质细胞的髓鞘形成。然而,形成的髓鞘节段明显短于野生型少突胶质细胞产生的髓鞘节段,这增加了神经胶质PTPα在髓鞘延伸中发挥作用的可能性,该作用与其促分化作用不同。总之,这项研究揭示PTPα是少突胶质细胞和神经元信号的分子协调者,可控制少突胶质细胞发育和髓鞘形成的多个方面。