Institute of Biomedical and Biomolecular Sciences, School of Pharmacy and Biomedical Science, University of Portsmouth, St. Michael's Building, White Swan Road, Portsmouth PO1 2DT, UK.
Section of Human Anatomy, Department of Neuroscience, University of Padua, 35122 Padua, Italy.
Cells. 2022 May 31;11(11):1809. doi: 10.3390/cells11111809.
The subventricular zone (SVZ) is the largest and most active germinal zone in the adult forebrain. Neural stem cells (NSCs) of the SVZ generate olfactory interneurons throughout life and retain the intrinsic ability to generate oligodendrocytes (OLs), the myelinating cells of the central nervous system. OLs and myelin are targets in demyelinating diseases such as multiple sclerosis (MS). Remyelination is dependent on the ability of oligodendrocyte progenitor cells (OPCs) to proliferate, migrate, and terminally differentiate into myelinating OLs. During aging, there is a gradual decrease in the regenerative capacity of OPCs, and the consequent loss of OLs and myelin is a contributing factor in cognitive decline and the failure of remyelination in MS and other pathologies with aging contexts, including Alzheimer's disease (AD) and stroke. The age-related decrease in oligodendrogenesis has not been fully characterised but is known to reflect changes in intrinsic and environmental factors affecting the ability of OPCs to respond to pro-differentiation stimuli. Notably, SVZ-derived OPCs are an important source of remyelinating OLs in addition to parenchymal OPCs. In this mini-review, we briefly discuss differences between SVZ-derived and parenchymal OPCs in their responses to demyelination and highlight challenges associated with their study in vivo and how they can be targeted for regenerative therapies in the aged brain.
室下区(SVZ)是成年前脑最大和最活跃的生殖区。SVZ 的神经干细胞(NSCs)终生产生嗅觉中间神经元,并保留内在能力产生少突胶质细胞(OLs),即中枢神经系统的髓鞘细胞。OLs 和髓鞘是多发性硬化症(MS)等脱髓鞘疾病的靶点。髓鞘再生依赖于少突胶质前体细胞(OPCs)的增殖、迁移和终末分化为髓鞘形成 OLs 的能力。随着年龄的增长,OPCs 的再生能力逐渐下降,OLs 和髓鞘的丧失是认知能力下降和 MS 及其他与衰老相关的病理学中髓鞘再生失败的一个促成因素,包括阿尔茨海默病(AD)和中风。与年龄相关的少突胶质生成减少尚未得到充分描述,但已知反映了内在和环境因素的变化,这些因素影响 OPCs 对促分化刺激的反应能力。值得注意的是,SVZ 衍生的 OPCs 是除实质 OPCs 之外髓鞘形成 OLs 的重要来源。在这篇迷你综述中,我们简要讨论了 SVZ 衍生的和实质的 OPCs 在对脱髓鞘反应方面的差异,并强调了它们在体内研究中的挑战,以及如何针对衰老大脑中的再生治疗来靶向它们。