Abstract
Dendritic spines mediate most excitatory neurotransmission in the nervous system, so their function must be critical for the brain. Spines are biochemical compartments but might also electrically modify synaptic potentials. Using two-photon microscopy and a genetically encoded voltage indicator, we measured membrane potentials in spines and dendrites from pyramidal neurons in the somatosensory cortex of mice during spontaneous activity and sensory stimulation. Spines and dendrites were depolarized together during action potentials, but, during subthreshold and resting potentials, spines often experienced different voltages than parent dendrites, even activating independently. Spine voltages remained compartmentalized after two-photon optogenetic activation of individual spine heads. We conclude that spines are elementary voltage compartments. The regulation of voltage compartmentalization could be important for synaptic function and plasticity, dendritic integration, and disease states.
Original language | English |
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Pages (from-to) | 82-86 |
Number of pages | 5 |
Journal | Science |
Volume | 375 |
Issue number | 6576 |
DOIs | |
State | Published - 7 Jan 2022 |
Bibliographical note
Publisher Copyright:© 2022 American Association for the Advancement of Science. All rights reserved.
Funding
We thank W. Stoy for comments and data in Fig. 1C and fig. S2C. R.Y. is an Ikerbasque Research Professor at the Donostia International Physics Center. This work is dedicated to the memory of Amiram Grinvald. This work was funded by National Institute of Neurological Disorders and Stroke (NINDS) grant R01NS110422 (R.Y.), NINDS grant R34NS116740 (R.Y.), National Eye Institute (NEI) grant R01EY011787 (R.Y.), National Institute of Mental Health (NIMH) grant R01MH115900 (R.Y.), and the PEW Latin American Fellows Program in Biomedical Sciences (V.H.C.).
Funders | Funder number |
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National Institute of Mental Health | R01MH115900 |
National Eye Institute | R01EY011787 |
National Institute of Neurological Disorders and Stroke | R34NS116740, R01NS110422 |