| Literature DB >> 30904575 |
Wanyi Jia1, Yasmine Kamen1, Helena Pivonkova1, Ragnhildur T Káradóttir2.
Abstract
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.Entities:
Keywords: Glia; Myelin; Myelination; Neuronal activity; Neurotransmitter; Oligodendrocyte precursor cell; Stroke
Mesh:
Year: 2019 PMID: 30904575 DOI: 10.1016/j.neulet.2019.03.005
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046