Badia-Soteras Aina, Mak Aline, Blok Thomas M, Boers-Escuder Cristina, van den Oever Michel C, Min Rogier, Smit August B, Verheijen Mark H G
Department of Molecular and Cellular Neuroscience, Center for Neurogenomics and Cognitive Research, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam, the Netherlands; Department of Brain Sciences, Imperial College London, London, United Kingdom; UK Dementia Research Institute at Imperial College London, London, United Kingdom.
Department of Molecular and Cellular Neuroscience, Center for Neurogenomics and Cognitive Research, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Amsterdam, the Netherlands.
Biol Psychiatry. 2025 Apr 18. doi: 10.1016/j.biopsych.2025.04.011.
Synaptic dysfunction is a common feature across a broad spectrum of brain diseases, spanning from psychopathologies such as posttraumatic stress disorder and substance use disorders to neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease. While neuroscience research aiming to understand the mechanisms underlying synaptic dysfunction has traditionally focused on the neuronal elements of the synapse, recent research increasingly acknowledges the contribution of astrocytes as a third element controlling synaptic transmission. This also sparked interest to investigate the tripartite synapse and its role in the etiology of neurological diseases. According to recent evidence, changes in the structural interaction between astrocytes and synapses not only play a pivotal role in modulating synaptic function and behavioral states, but also are implicated in the initiation and progression of various brain diseases. This review aims to integrate recent findings that provide insight into the molecular mechanisms underpinning astrocytic structural changes at the synapse. We present a comprehensive discussion of the potential implications of compromised astrocyte-synapse interactions and suggest that astrocytic synaptic coverage is generally reduced in numerous neurological disorders, with the extent of it being disease and stage specific. Finally, we propose outstanding questions on astrocyte-synapse structural plasticity that are relevant for future therapeutic strategies to address neurodegenerative and neuropsychiatric diseases.
突触功能障碍是多种脑部疾病的共同特征,涵盖从创伤后应激障碍和物质使用障碍等精神病理学疾病到阿尔茨海默病和帕金森病等神经退行性疾病。虽然旨在了解突触功能障碍潜在机制的神经科学研究传统上侧重于突触的神经元成分,但最近的研究越来越认识到星形胶质细胞作为控制突触传递的第三个元素的作用。这也引发了对三方突触及其在神经疾病病因学中作用的研究兴趣。根据最近的证据,星形胶质细胞与突触之间结构相互作用的变化不仅在调节突触功能和行为状态中起关键作用,而且还与各种脑部疾病的发生和发展有关。本综述旨在整合最近的研究结果,这些结果有助于深入了解突触处星形胶质细胞结构变化的分子机制。我们全面讨论了星形胶质细胞 - 突触相互作用受损的潜在影响,并表明在许多神经疾病中,星形胶质细胞的突触覆盖通常会减少,其程度因疾病和阶段而异。最后,我们提出了关于星形胶质细胞 - 突触结构可塑性的突出问题,这些问题与未来治疗神经退行性和神经精神疾病的策略相关。