Wellcome - Medical Research Council Cambridge Stem Cell Institute & Department of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom.
Wellcome - Medical Research Council Cambridge Stem Cell Institute & Department of Veterinary Medicine, University of Cambridge, Cambridge, United Kingdom; Department of Physiology, BioMedical Center, Faculty of Medicine, University of Iceland, Reykjavik, Iceland.
Neurosci Lett. 2019 Jun 11;703:139-144. doi: 10.1016/j.neulet.2019.03.005. Epub 2019 Mar 20.
Brain tissue undergoes substantial activity-dependent reorganisation after stroke due to neuronal plasticity, leading to partial functional recovery in patients. Concurrent myelin repair is crucial for proper neuronal network function and reorganisation. Myelin repair after stroke might occur as myelin plasticity or as remyelination through the recruitment and differentiation of oligodendrocyte precursor cells (OPCs), which become myelin-forming oligodendrocytes (OLs). These two processes might share a similar guiding mechanism, which is postulated to depend on neuronal activity and glutamate signaling to OPCs. However, with ageing, the ability of OPCs to differentiate into myelinating OLs decreases due to changes in their ion channel and neurotransmitter receptor expression profile, rendering them less sensitive to neuronal activity. Because of their unique ability to replace damaged OLs, OPCs represent a potential therapeutic target for myelin repair in the context of stroke.
脑损伤后,由于神经元可塑性,脑组织会发生大量的活性依赖性重组,从而导致患者部分功能恢复。髓鞘修复对于正常的神经元网络功能和重组至关重要。中风后的髓鞘修复可能通过少突胶质细胞前体细胞(OPC)的募集和分化发生,形成髓鞘形成少突胶质细胞(OL),即髓鞘可塑性;也可能通过髓鞘修复发生,即少突胶质细胞前体细胞(OPC)募集和分化形成髓鞘形成少突胶质细胞(OL)。这两个过程可能具有相似的指导机制,该机制被认为依赖于神经元活性和谷氨酸信号转导至少突胶质细胞前体细胞(OPC)。然而,随着年龄的增长,少突胶质细胞前体细胞(OPC)分化为髓鞘形成少突胶质细胞(OL)的能力会下降,这是由于其离子通道和神经递质受体表达谱发生变化,使其对神经元活性的敏感性降低。由于其独特的能力能够替代受损的 OL,少突胶质细胞前体细胞(OPC)在中风的背景下代表了髓鞘修复的一个潜在治疗靶点。