Department of Pharmacology and Physiology, Georgetown University Medical Center, Washington, DC, USA.
Department of Biology, Georgetown University, Washington, DC, USA.
Cell Mol Neurobiol. 2023 Mar;43(2):697-709. doi: 10.1007/s10571-022-01227-2. Epub 2022 May 28.
The field of homeostatic plasticity continues to advance rapidly, highlighting the importance of stabilizing neuronal activity within functional limits in the context of numerous fundamental processes such as development, learning, and memory. Most homeostatic plasticity studies have been focused on glutamatergic synapses, while the rules that govern homeostatic regulation of other synapse types are less understood. While cholinergic synapses have emerged as a critical component in the etiology of mammalian neurodegenerative disease mechanisms, relatively few studies have been conducted on the homeostatic plasticity of such synapses, particularly in the mammalian nervous system. An exploration of homeostatic mechanisms at the cholinergic synapse may illuminate potential therapeutic targets for disease management and treatment. We will review cholinergic homeostatic plasticity in the mammalian neuromuscular junction, the autonomic nervous system, central synapses, and in relation to pathological conditions including Alzheimer disease and DYT1 dystonia. This work provides a historical context for the field of cholinergic homeostatic regulation by examining common themes, unique features, and outstanding questions associated with these distinct cholinergic synapse types and aims to inform future research in the field.
内稳态可塑性领域继续快速发展,突出了在发育、学习和记忆等许多基本过程中,将神经元活动稳定在功能范围内的重要性。大多数内稳态可塑性研究都集中在谷氨酸能突触上,而其他突触类型的内稳态调节规则则了解较少。虽然胆碱能突触已成为哺乳动物神经退行性疾病机制病因的关键组成部分,但对这类突触的内稳态可塑性的研究相对较少,特别是在哺乳动物神经系统中。探索胆碱能突触的内稳态机制可能为疾病管理和治疗提供潜在的治疗靶点。我们将回顾哺乳动物神经肌肉接头、自主神经系统、中枢突触中的胆碱能内稳态可塑性,以及与包括阿尔茨海默病和 DYT1 型肌张力障碍在内的病理状况的关系。这项工作通过检查与这些不同的胆碱能突触类型相关的共同主题、独特特征和悬而未决的问题,为胆碱能内稳态调节领域提供了历史背景,并旨在为该领域的未来研究提供信息。