Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China; State Key Laboratory of Molecular Neuroscience, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China; Molecular Neuroscience Center, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China; Guangdong Provincial Key Laboratory of Brain Science, Disease and Drug Development, HKUST Shenzhen Research Institute, Shenzhen, Guangdong 518057, China.
Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China; State Key Laboratory of Molecular Neuroscience, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China; Molecular Neuroscience Center, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China; Guangdong Provincial Key Laboratory of Brain Science, Disease and Drug Development, HKUST Shenzhen Research Institute, Shenzhen, Guangdong 518057, China.
Curr Opin Neurobiol. 2017 Aug;45:148-155. doi: 10.1016/j.conb.2017.05.016. Epub 2017 Jun 7.
Morphological changes of dendritic spines are strongly associated with synaptic development and synaptic plasticity, which underlies learning and memory. These changes are driven by alterations of F-actin dynamics under the control of Rho GTPases or by synaptic trafficking and insertion of glutamate receptors. Understanding the molecular events that occur during the formation and stabilization of dendritic spines, and the signaling pathways regulating these processes, provides insights into the mechanisms of learning and memory. In this review, we discuss the recent advances on these postsynaptic signaling pathways, in particular, we discuss the specific signaling events that couple the cell-surface receptors to intracellular targets. In addition, we discuss the deregulation of these signaling pathways and their subsequent impact on synaptic dysfunction in Alzheimer's disease.
树突棘形态变化与突触发育和突触可塑性密切相关,而后者是学习和记忆的基础。这些变化是由 Rho GTPases 控制下的 F-肌动蛋白动力学改变或谷氨酸受体的突触运输和插入驱动的。了解树突棘形成和稳定过程中发生的分子事件,以及调节这些过程的信号通路,为学习和记忆的机制提供了深入的认识。在这篇综述中,我们讨论了这些突触后信号通路的最新进展,特别是讨论了将细胞表面受体与细胞内靶标偶联的特定信号事件。此外,我们还讨论了这些信号通路的失调及其对阿尔茨海默病中突触功能障碍的后续影响。