期刊文献+
共找到3篇文章
< 1 >
每页显示 20 50 100
Myelin in development and disease
1
作者 Mengsheng Qiu 《Neuroscience Bulletin》 SCIE CAS CSCD 2013年第2期127-128,共2页
Myelin is an evolutionarUy novel and important structure for the proper functioning of the vertebrate nervous system. In the central nervous system (CNS), the myelin sheath is elaborated by oligodendrocytes, and is ... Myelin is an evolutionarUy novel and important structure for the proper functioning of the vertebrate nervous system. In the central nervous system (CNS), the myelin sheath is elaborated by oligodendrocytes, and is composed of multiple layers of specialized cell membrane wrapping around axons with periodic interruptions at the nodes of Ranvier. The major function of the myelin sheath is to provide ionic insulation to ensure rapid and saltatory conduction of electrical pulses along axons. In addition, myelin provides neurotrophic support for axons, as they become increasingly dependent on myelin-derived signals for survival. Despite the importance of myelin in the functioning of the CNS, oligodendrocytes are particularly susceptible to genetic and environmental perturbations, and demyelination can be triggered by many pathological conditions including traumatic injury, autoimmune disease (multiple sclerosis, MS), heavy metal toxicity, and hypoxia. Loss of myelin sheaths in the CNS not only results in the compromised conduction of electrical signals, but also causes progressive degeneration of axons and ultimately neuronal loss. Spontaneous myelin repair from immature oligodendrocyte progenitor cells (OPCs) is not effective in demyelinating lesions, due either to the absence of stimulatory developmental signals that are no longer produced in the adult environment, or to the presence of inhibitory factors peculiar to this environment. 展开更多
关键词 myelin in development and disease
原文传递
Embracing oligodendrocyte diversity in the context of perinatal injury 被引量:1
2
作者 Jessie Newville Lauren L.Jantzie Lee Anna Cunningham 《Neural Regeneration Research》 SCIE CAS CSCD 2017年第10期1575-1585,共11页
Emerging evidence is fueling a new appreciation of oligodendrocyte diversity that is overturning the traditional view that oligodendrocytes are a homogenous cell population.Oligodendrocytes of distinct origins,maturat... Emerging evidence is fueling a new appreciation of oligodendrocyte diversity that is overturning the traditional view that oligodendrocytes are a homogenous cell population.Oligodendrocytes of distinct origins,maturational stages,and regional locations may differ in their functional capacity or susceptibility to injury.One of the most unique qualities of the oligodendrocyte is its ability to produce myelin.Myelin abnormalities have been ascribed to a remarkable array of perinatal brain injuries,with concomitant oligodendrocyte dysregulation.Within this review,we discuss new insights into the diversity of the oligodendrocyte lineage and highlight their relevance in paradigms of perinatal brain injury.Future therapeutic development will be informed by comprehensive knowledge of oligodendrocyte pathophysiology that considers the particular facets of heterogeneity that this lineage exhibits. 展开更多
关键词 oligodendrogenesis oligodendrocyte progenitor cell myelination central nervous system development ontogenetic origin white matter white matter injury preterm birth glia macroglia
暂未订购
神经生长因子通过促进少突胶质前体细胞分化改善脑组织缺血低氧的实验研究
3
作者 刘萍萍 何学芳 +3 位作者 张翼 杨旭 张珊珊 季一飞 《脑与神经疾病杂志》 CAS 2024年第8期467-473,共7页
目的探讨神经生长因子(NGF)改善脑组织低氧缺血状态作用机制。方法本研究通过培养混合神经干细胞(NSC)衍生的少突胶质细胞前体细胞(OPC)/星形胶质细胞培养来阐明神经生长因子在整个少突胶质细胞(OL)分化过程中的作用,并探讨其在缺血低... 目的探讨神经生长因子(NGF)改善脑组织低氧缺血状态作用机制。方法本研究通过培养混合神经干细胞(NSC)衍生的少突胶质细胞前体细胞(OPC)/星形胶质细胞培养来阐明神经生长因子在整个少突胶质细胞(OL)分化过程中的作用,并探讨其在缺血低氧状态条件下对OPC的保护作用。结果共聚焦显微镜检查结果显示,GW-44175610μM处理组细胞凝聚核百分比显著高于0.1μM、1μM及NGF抗体组(P<0.05)。抗NGF抗体处理组及GW-4417561μM处理组分化末期OPC百分比显著高于其他组(P<0.05)。抗NGF抗体处理组及GW-44175610μM处理组成熟OL及成髓鞘OPC百分比显著低于其他组(P<0.05)。抗NGF抗体处理组及GW-44175处理组NG2-阳性细胞比例显著高于其他组(P<0.05);抗NGF抗体处理组及GW-44175处理组CNPase/MBP染色细胞比例显著低于其他组(P<0.05);GW-441756处理组GFAP染色细胞比例显著高于其他组(P<0.05)。共聚焦显微镜检查结果显示,OGD处理组星形胶质细胞NGF mRNA表达水平显著高于无OGD处理组(P<0.05);NGF处理组细胞核内蛋白激酶B(AKT)荧光强度水平显著高于无NGF处理组(P<0.05);NGF处理组细胞核中磷酸化AKT荧光强度显著高于无NGF处理组、神经生长因子抗体(Ab-NGF)处理组及原肌球蛋白受体激酶A(TRKA)拮抗剂组(P<0.05)。结论NGF在体外细胞培养中与星形胶质细胞的相互作用可调节OPC生理分化;同时在缺血低氧状态下其对于OPC存活及OL成熟具有明确保护作用。 展开更多
关键词 神经生长因子 少突胶质前体细胞 缺血低氧 发育性髓鞘
暂未订购
上一页 1 下一页 到第
使用帮助 返回顶部