Literature DB >> 15617680

Dynamics of dendritic spines and their afferent terminals: spines are more motile than presynaptic boutons.

Jinbo Deng1, Anna Dunaevsky.   

Abstract

Previous work has established that dendritic spines, sites of excitatory input in CNS neurons, can be highly dynamic, in later development as well as in mature brain. Although spine motility has been proposed to facilitate the formation of new synaptic contacts, we have reported that spines continue to be dynamic even if they bear synaptic contacts. An outstanding question related to this finding is whether the presynaptic terminals that contact dendritic spines are as dynamic as their postsynaptic targets. Using multiphoton time-lapse microscopy of GFP-labeled Purkinje cells and DiI-labeled granule cell parallel fiber afferents in cerebellar slices, we monitored the dynamic behavior of both presynaptic terminals and postsynaptic dendritic spines in the same preparation. We report that while spines are dynamic, the presynaptic terminals they contact are quite stable. We confirmed the relatively low levels of presynaptic terminal motility by imaging parallel fibers in vivo. Finally, spine motility can occur when a functional presynaptic terminal is apposed to it. These analyses further call into question the function of spine motility, and to what extent the synapse breaks or maintains its contact during the movement of the spine.

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Year:  2005        PMID: 15617680     DOI: 10.1016/j.ydbio.2004.09.028

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  12 in total

1.  Bergmann glial ensheathment of dendritic spines regulates synapse number without affecting spine motility.

Authors:  Jocelyn J Lippman Bell; Tamar Lordkipanidze; Natalie Cobb; Anna Dunaevsky
Journal:  Neuron Glia Biol       Date:  2010-11-02

2.  The synaptic remodeling between regenerated perforant pathway and granule cells in slice culture.

Authors:  Dong-Ming Yu; Wen-Chun Tang; Ping Wu; Tong-Xing Deng; Bin Liu; Ming-Shan Li; Jin-Bo Deng
Journal:  Cell Mol Neurobiol       Date:  2009-09-16       Impact factor: 5.046

3.  The long-term structural plasticity of cerebellar parallel fiber axons and its modulation by motor learning.

Authors:  Jennifer Carrillo; Shao-Ying Cheng; Kwang Woo Ko; Theresa A Jones; Hiroshi Nishiyama
Journal:  J Neurosci       Date:  2013-05-08       Impact factor: 6.167

4.  Early-life adversity selectively interrupts the dendritic differentiation of dorsolateral striatal neurons in male mice.

Authors:  Yun He; Benke Xu; Yan Chen; Lian Liu; Liping Xu; Yuncai Chen; Dahong Long
Journal:  Brain Struct Funct       Date:  2021-01-02       Impact factor: 3.270

5.  A stable proportion of Purkinje cell inputs from parallel fibers are silent during cerebellar maturation.

Authors:  Shu Ho; Rebecca Lajaunie; Marion Lerat; Mickaël Le; Valérie Crépel; Karine Loulier; Jean Livet; Jean-Pierre Kessler; Païkan Marcaggi
Journal:  Proc Natl Acad Sci U S A       Date:  2021-11-09       Impact factor: 11.205

6.  Degenerating synaptic boutons in prion disease: microglia activation without synaptic stripping.

Authors:  Zuzana Sisková; Anton Page; Vincent O'Connor; Victor Hugh Perry
Journal:  Am J Pathol       Date:  2009-09-24       Impact factor: 4.307

7.  Modifications of gustatory nerve synapses onto nucleus of the solitary tract neurons induced by dietary sodium-restriction during development.

Authors:  Olivia L May; Alev Erisir; David L Hill
Journal:  J Comp Neurol       Date:  2008-06-01       Impact factor: 3.215

8.  Neuron-glial interactions in the developing cerebellum.

Authors:  Anna Dunaevsky
Journal:  Microsc Microanal       Date:  2012-07-26       Impact factor: 4.127

9.  Phase-specific plasticity of synaptic structures in the somatosensory cortex of living mice during neuropathic pain.

Authors:  Sun Kwang Kim; Go Kato; Tatsuya Ishikawa; Junichi Nabekura
Journal:  Mol Pain       Date:  2011-11-09       Impact factor: 3.395

10.  Developmental expression and differentiation-related neuron-specific splicing of metastasis suppressor 1 (Mtss1) in normal and transformed cerebellar cells.

Authors:  Alexander Glassmann; Sabine Molly; Lachezar Surchev; Tommy A Nazwar; Martin Holst; Wolfgang Hartmann; Stephan L Baader; John Oberdick; Torsten Pietsch; Karl Schilling
Journal:  BMC Dev Biol       Date:  2007-10-09       Impact factor: 1.978

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