Department of Pharmacology, JSS College of Pharmacy, JSS Academy of Higher Education & Research (JSSAHER), Mysuru, Karnataka 570015, India.
Food and Brain Research Foundation, Chennai, Tamil Nadu, India.
Prog Neuropsychopharmacol Biol Psychiatry. 2019 Jun 8;92:161-193. doi: 10.1016/j.pnpbp.2019.01.005. Epub 2019 Jan 15.
Dendritic spines are small, thin, specialized protrusions from neuronal dendrites, primarily localized in the excitatory synapses. Sophisticated imaging techniques revealed that dendritic spines are complex structures consisting of a dense network of cytoskeletal, transmembrane and scaffolding molecules, and numerous surface receptors. Molecular signaling pathways, mainly Rho and Ras family small GTPases pathways that converge on actin cytoskeleton, regulate the spine morphology and dynamics bi-directionally during synaptic activity. During synaptic plasticity the number and shapes of dendritic spines undergo radical reorganizations. Long-term potentiation (LTP) induction promote spine head enlargement and the formation and stabilization of new spines. Long-term depression (LTD) results in their shrinkage and retraction. Reports indicate increased spine density in the pyramidal neurons of autism and Fragile X syndrome patients and reduced density in the temporal gyrus loci of schizophrenic patients. Post-mortem reports of Alzheimer's brains showed reduced spine number in the hippocampus and cortex. This review highlights the spine morphogenesis process, the activity-dependent structural plasticity and mechanisms by which synaptic activity sculpts the dendritic spines, the structural and functional changes in spines during learning and memory using LTP and LTD processes. It also discusses on spine status in neurodegenerative diseases and the impact of nootropics and neuroprotective agents on the functional restoration of dendritic spines.
树突棘是神经元树突上的小而细的特化突起,主要位于兴奋性突触。复杂的成像技术揭示了树突棘是由细胞骨架、跨膜和支架分子的密集网络以及许多表面受体组成的复杂结构。分子信号通路,主要是 Rho 和 Ras 家族的小 GTPases 通路,它们汇聚在肌动蛋白细胞骨架上,在突触活动期间双向调节棘形态和动力学。在突触可塑性过程中,树突棘的数量和形状会发生剧烈的重组。长时程增强(LTP)诱导促进棘头增大和新棘的形成和稳定。长时程抑制(LTD)导致其收缩和缩回。研究报告表明,自闭症和脆性 X 综合征患者的锥体神经元中树突棘密度增加,精神分裂症患者颞叶回的密度降低。阿尔茨海默病大脑的尸检报告显示,海马体和皮质中的棘突数量减少。本综述重点介绍了棘突形态发生过程、活动依赖性结构可塑性以及突触活动对树突棘的塑造机制、LTP 和 LTD 过程中学习和记忆过程中棘突的结构和功能变化。它还讨论了神经退行性疾病中的棘突状态以及益智药和神经保护剂对树突棘功能恢复的影响。