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The Journal of Neuroscience, August 15, 2001, 21(16):6115-6124
Regulation of Dendritic Spine Motility in Cultured
Hippocampal Neurons
Eduard
Korkotian and
Menahem
Segal
Department of Neurobiology, The Weizmann Institute, Rehovot 76100, Israel
Regulation of dendritic spine motility was studied in dissociated
cultures of the rat and mouse hippocampus, using green fluorescent protein-labeled neurons or neurons loaded with the calcium-sensitive dye Oregon Green-1. Cells were time-lapse-photographed on a
confocal laser-scanning microscope at high resolution to detect
movements as well as spontaneous fluctuations of intracellular calcium
concentrations in their dendritic spines. Active presynaptic terminals
attached to the spines were labeled with FM4-64, which marks a
subset of synaptophysin-labeled terminals. Dendritic spines were highly motile in young, 4- to 7-d-old cells. At this age, neurons had little
spontaneous calcium fluctuation or FM4-64 labeling. Within 2-3 weeks
in culture, dendritic spines were much less motile, they were
associated with active presynaptic terminals, and they expressed high
rates of spontaneous calcium fluctuations. Irrespective of age, and
even on the same dendrite, there was an inverse relationship between
spine motility and presence of FM4-64-labeled terminals in contact with
the imaged spines. Spine motility was blocked by latrunculin, which
prevents actin polymerization, and was disinhibited by blockade of
action potential discharges with tetrodotoxin. It is proposed that an
active presynaptic terminal restricts motility of dendritic spines.
Key words:
dendritic spines; confocal microscope; EGFP; FM4-64; calcium; actin; latrunculin
Copyright © 2001 Society for Neuroscience 0270-6474/01/21166115-10$05.00/0
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