The Spread of Ras Activity Triggered by Activation of a Single Dendritic Spine

Author:

Harvey Christopher D.123,Yasuda Ryohei123,Zhong Haining123,Svoboda Karel123

Affiliation:

1. Janelia Farm Research Campus, Howard Hughes Medical Institute, Ashburn, VA 20147, USA.

2. Watson School of Biological Sciences, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.

3. Neurobiology Department, Duke University Medical Center, Durham, NC 27710, USA.

Abstract

In neurons, individual dendritic spines isolate N -methyl- d -aspartate (NMDA) receptor–mediated calcium ion (Ca 2+ ) accumulations from the dendrite and other spines. However, the extent to which spines compartmentalize signaling events downstream of Ca 2+ 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 Ca 2+ -dependent Ras activation in single spines that decayed in ∼5 minutes. Ras activity spread over ∼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, Ca 2+ -dependent synaptic signals can spread to couple multiple synapses on short stretches of dendrite.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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