Precise Temporal Regulation of Molecular Diffusion within Dendritic Spines by Actin Polymers during Structural Plasticity

Summary: The biochemical transduction of excitatory synaptic signals occurs in the cytoplasm within dendritic spines. The associated reaction kinetics are shaped by the mobility of the signaling molecules; however, accurate monitoring of diffusional events within the femtoliter-sized spine structure...

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Main Authors: Kazuki Obashi, Atsushi Matsuda, Yasuhiro Inoue, Shigeo Okabe
Format: Article
Language:English
Published: Elsevier 2019-04-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124719304619
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author Kazuki Obashi
Atsushi Matsuda
Yasuhiro Inoue
Shigeo Okabe
author_facet Kazuki Obashi
Atsushi Matsuda
Yasuhiro Inoue
Shigeo Okabe
author_sort Kazuki Obashi
collection DOAJ
description Summary: The biochemical transduction of excitatory synaptic signals occurs in the cytoplasm within dendritic spines. The associated reaction kinetics are shaped by the mobility of the signaling molecules; however, accurate monitoring of diffusional events within the femtoliter-sized spine structures has not yet been demonstrated. Here, we applied two-photon fluorescence correlation spectroscopy and raster image correlation spectroscopy to monitor protein dynamics within spines, revealing that F-actin restricts the mobility of proteins with a molecular mass of >100 kDa. This restriction is transiently removed during actin remodeling at the initial phase of spine structural plasticity. Photobleaching experiments combined with super-resolution imaging indicate that this increase in mobility facilitates molecular interactions, which may modulate the functions of key postsynaptic signaling molecules, such as Tiam1 and CaMKII. Thus, actin polymers in dendritic spines act as precise temporal regulators of molecular diffusion and modulate signal transduction during synaptic plasticity. : Obashi et al. show that actin polymers within dendritic spines restrict mobility of large molecules using optical measurements of fluorescence correlation. Acute actin remodeling induced by plasticity-inducing stimuli increases the mobility of large postsynaptic signaling molecules, which regulate long-term changes in synaptic property. Keywords: dendritic spine, synaptic plasticity, actin cytoskeleton, molecular mobility, FCS, RICS, super-resolution microscopy, Tiam1, calcium/calmodulin-dependent protein kinase, Brownian dynamics simulation
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spelling doaj.art-24d51b96abda4761ae3aced2e49be39e2022-12-22T01:16:42ZengElsevierCell Reports2211-12472019-04-0127515031515.e8Precise Temporal Regulation of Molecular Diffusion within Dendritic Spines by Actin Polymers during Structural PlasticityKazuki Obashi0Atsushi Matsuda1Yasuhiro Inoue2Shigeo Okabe3Department of Cellular Neurobiology, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, JapanInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto 606-8507, JapanInstitute for Frontier Life and Medical Sciences, Kyoto University, Kyoto 606-8507, JapanDepartment of Cellular Neurobiology, Graduate School of Medicine, The University of Tokyo, Tokyo 113-0033, Japan; Corresponding authorSummary: The biochemical transduction of excitatory synaptic signals occurs in the cytoplasm within dendritic spines. The associated reaction kinetics are shaped by the mobility of the signaling molecules; however, accurate monitoring of diffusional events within the femtoliter-sized spine structures has not yet been demonstrated. Here, we applied two-photon fluorescence correlation spectroscopy and raster image correlation spectroscopy to monitor protein dynamics within spines, revealing that F-actin restricts the mobility of proteins with a molecular mass of >100 kDa. This restriction is transiently removed during actin remodeling at the initial phase of spine structural plasticity. Photobleaching experiments combined with super-resolution imaging indicate that this increase in mobility facilitates molecular interactions, which may modulate the functions of key postsynaptic signaling molecules, such as Tiam1 and CaMKII. Thus, actin polymers in dendritic spines act as precise temporal regulators of molecular diffusion and modulate signal transduction during synaptic plasticity. : Obashi et al. show that actin polymers within dendritic spines restrict mobility of large molecules using optical measurements of fluorescence correlation. Acute actin remodeling induced by plasticity-inducing stimuli increases the mobility of large postsynaptic signaling molecules, which regulate long-term changes in synaptic property. Keywords: dendritic spine, synaptic plasticity, actin cytoskeleton, molecular mobility, FCS, RICS, super-resolution microscopy, Tiam1, calcium/calmodulin-dependent protein kinase, Brownian dynamics simulationhttp://www.sciencedirect.com/science/article/pii/S2211124719304619
spellingShingle Kazuki Obashi
Atsushi Matsuda
Yasuhiro Inoue
Shigeo Okabe
Precise Temporal Regulation of Molecular Diffusion within Dendritic Spines by Actin Polymers during Structural Plasticity
Cell Reports
title Precise Temporal Regulation of Molecular Diffusion within Dendritic Spines by Actin Polymers during Structural Plasticity
title_full Precise Temporal Regulation of Molecular Diffusion within Dendritic Spines by Actin Polymers during Structural Plasticity
title_fullStr Precise Temporal Regulation of Molecular Diffusion within Dendritic Spines by Actin Polymers during Structural Plasticity
title_full_unstemmed Precise Temporal Regulation of Molecular Diffusion within Dendritic Spines by Actin Polymers during Structural Plasticity
title_short Precise Temporal Regulation of Molecular Diffusion within Dendritic Spines by Actin Polymers during Structural Plasticity
title_sort precise temporal regulation of molecular diffusion within dendritic spines by actin polymers during structural plasticity
url http://www.sciencedirect.com/science/article/pii/S2211124719304619
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AT yasuhiroinoue precisetemporalregulationofmoleculardiffusionwithindendriticspinesbyactinpolymersduringstructuralplasticity
AT shigeookabe precisetemporalregulationofmoleculardiffusionwithindendriticspinesbyactinpolymersduringstructuralplasticity