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Ultrastructural analysis of neuronal synapses using cryo electron tomography and correlative microscopy

机译:低温电子层析成像和相关显微镜对神经元突触的超微结构分析

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Synapse elimination processes have also been observed during synaptic plasticity in the adult brain, such as when sensory experience induces the formation of new spines and eliminates pre-existing spines during learning and memory formation. Thus, synapse elimination is likely a central feature of nervous system remodeling and reorganization throughout the lifespan. Moreover, certain neurodegenerative diseases, such as Alzheimer’s disease, are associated with profound synapse loss early in the disease state, underscoring the importance of under- standing the molecular mechanisms underlying this synapse loss. Recently, we found that astrocytes in the mouse visual system and hippocampus mediate synapse remodeling by actively engulfing weak but live synapses through phagocytosis and that this process is regulated by neuronal activity. Furthermore, we have found evi- dence that defective astrocyte-mediated synapse elimination can be a critical link to the initiation and progression of neurodegener- ative diseases, such as Alzheimer’s disease. This data suggests that astrocytes can participate in the constant remodeling of synaptic structures through our life in the healthy and diseased brain.
机译:在成人大脑中的突触可塑性过程中,例如在感官体验诱导新的棘突形成并消除学习和记忆形成过程中先前存在的棘突时,也已经观察到突触消除过程。因此,消除突触可能是整个寿命过程中神经系统重塑和重组的主要特征。此外,某些神经退行性疾病,例如阿尔茨海默氏病,在疾病初期与突触的大量丧失有关,这突显了理解这种突触丧失的分子机制的重要性。最近,我们发现小鼠视觉系统和海马中的星形胶质细胞通过吞噬作用吞噬弱而活的突触来介导突触重塑,并且该过程受神经元活动的调节。此外,我们发现有缺陷的星形胶质细胞介导的突触消除可能与神经退行性疾病(例如阿尔茨海默氏病)的发生和发展有着关键的联系。这些数据表明星形胶质细胞可以在我们健康和患病的大脑中参与我们生命中突触结构的不断重塑。

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