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The Spread of Ras Activity Triggered by Activation of a Single Dendritic Spine
Author(s) -
Christopher D. Harvey,
Ryohei Yasuda,
Haining Zhong,
Karel Svoboda
Publication year - 2008
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1159675
Subject(s) - dendritic spine , long term potentiation , nmda receptor , dendrite (mathematics) , dendritic filopodia , biophysics , spine (molecular biology) , chemistry , apical dendrite , biology , microbiology and biotechnology , neuroscience , receptor , biochemistry , cerebral cortex , hippocampal formation , geometry , mathematics
In neurons, individual dendritic spines isolate N-methyl-d-aspartate (NMDA) receptor-mediated calcium ion (Ca2+) accumulations from the dendrite and other spines. However, the extent to which spines compartmentalize signaling events downstream of Ca2+ influx is not known. We combined two-photon fluorescence lifetime imaging with two-photon glutamate uncaging to image the activity of the small guanosine triphosphatase Ras after NMDA receptor activation at individual spines. Induction of long-term potentiation (LTP) triggered robust Ca2+-dependent Ras activation in single spines that decayed in approximately 5 minutes. Ras activity spread over approximately 10 micrometers of dendrite and invaded neighboring spines by diffusion. The spread of Ras-dependent signaling was necessary for the local regulation of the threshold for LTP induction. Thus, Ca2+-dependent synaptic signals can spread to couple multiple synapses on short stretches of dendrite.

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