阿尔茨海默病中的突触代偿性可塑性。

Synaptic Compensatory Plasticity in Alzheimer's Disease.

机构信息

Clem Jones Centre for Ageing Dementia Research, Queensland Brain Institute, University of Queensland, Brisbane, Queensland 4072, Australia.

UK Dementia Research Institute, Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh Medical School, Edinburgh, EH16 4SB, United Kingdom.

出版信息

J Neurosci. 2023 Oct 11;43(41):6833-6840. doi: 10.1523/JNEUROSCI.0379-23.2023.

Abstract

The loss of excitatory synapses is known to underlie the cognitive deficits in Alzheimer's disease (AD). Although much is known about the mechanisms underlying synaptic loss in AD, how neurons compensate for this loss and whether this provides cognitive benefits remain almost completely unexplored. In this review, we describe two potential compensatory mechanisms implemented following synaptic loss: the enlargement of the surviving neighboring synapses and the regeneration of synapses. Because dendritic spines, the postsynaptic site of excitatory synapses, are easily visualized using light microscopy, we focus on a range of microscopy approaches to monitor synaptic loss and compensation. Here, we stress the importance of longitudinal dendritic spine imaging, as opposed to fixed-tissue imaging, to gain insights into the temporal dynamics of dendritic spine compensation. We believe that understanding the molecular mechanisms behind these and other forms of synaptic compensation and regeneration will be critical for the development of therapeutics aiming at delaying the onset of cognitive deficits in AD.

摘要

兴奋性突触的丧失是阿尔茨海默病(AD)认知缺陷的基础。尽管人们已经了解了 AD 中突触丧失的机制,但神经元如何补偿这种丧失,以及这种补偿是否能带来认知益处,仍然几乎完全没有得到探索。在这篇综述中,我们描述了两种可能的补偿机制:存活的相邻突触的增大和突触的再生。由于树突棘是兴奋性突触的突触后位点,使用光学显微镜很容易观察到,因此我们专注于一系列显微镜方法来监测突触的丧失和补偿。在这里,我们强调了纵向树突棘成像的重要性,而不是固定组织成像,以深入了解树突棘补偿的时间动态。我们相信,了解这些和其他形式的突触补偿和再生背后的分子机制对于开发旨在延缓 AD 认知缺陷发生的治疗方法将是至关重要的。

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