Spatiotemporal Regulation of Signaling in and out of Dendritic Spines: CaMKII and Ras.

Seok-Jin R Lee, Ryohei Yasuda
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Abstract

Recent advances in 2-photon fluorescence lifetime imaging microscopy (2pFLIM) in combination with 2-photon photochemistry have enabled the visualization of neuronal signaling during synaptic plasticity at the level of single dendritic spines in light scattering tissue. Using these techniques, the activity of Ca(2+)/Calmodulin-dependent kinase II (CaMKII) and Ras have been imaged in single spines during synaptic plasticity and associated spine enlargement. These provide two contrasting examples of spatiotemporal regulation of spine signaling: Ras signaling is diffusive and spread over ~10 μm along the dendrites, while CaMKII activation is restricted to the spine undergoing plasticity. In this review, we will discuss the mechanisms and roles of the different spatiotemporal regulation of signaling in neurons, and the impact of the spine structure upon these biochemical signaling processes.

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树突棘内外信号传递的时空调控:CaMKII 和 Ras
双光子荧光寿命成像显微镜(2pFLIM)结合双光子光化学技术的最新进展,使得在光散射组织中单个树突棘水平上可视化突触可塑性过程中的神经元信号传导成为可能。利用这些技术,我们对突触可塑性和相关棘突增大过程中单个棘突中 Ca(2+)/Calmodulin 依赖性激酶 II (CaMKII) 和 Ras 的活性进行了成像。这为脊柱信号的时空调控提供了两个截然不同的例子:Ras 信号是扩散性的,沿树突扩散约 10 μm,而 CaMKII 的激活仅限于发生可塑性的脊柱。在这篇综述中,我们将讨论神经元中不同时空调控信号传导的机制和作用,以及脊柱结构对这些生化信号传导过程的影响。
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