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Highly attenuated dendritic propagation of isolated synaptic potentials in vivo.

Overview

  1. Neurotechnology Center, Department of Biological Sciences, Columbia University, New York, NY 10027, USA
  2. Department of Bioengineering, Stanford University, Stanford, CA 94305, USA
Institutions: Columbia University (United States); Stanford University (United States)
Journal: Science advances, volume 12, issue 33, article eadz4123
Dates: received 30 May 2025; accepted 6 July 2026; published online 14 August 2026; in print August 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1126/sciadv.adz4123 · PMID 42600022 · PMCID PMC13475487 · OpenAlex W7203449353
Open access: gold, a free copy (OpenAlex)
Status: code verified
Categories: intracellular / patch clamp (modality), mouse (organism), cellular / molecular (subfield)
Methods: Preprocessing, Smoothing, state filtering, decompositions, Connectivity, Statistics, fMRI & imaging, Single-unit activity, calcium imaging
MeSH: Dendrites*, Pyramidal Cells*, Synapses*, Synaptic Potentials*, Action Potentials, Animals, Mice, Optogenetics, Patch-Clamp Techniques, Somatosensory Cortex, Synaptic Transmission (* major topic)
Journal subjects: Neuroscience, Neurophysiology
Topic: Neural dynamics and brain function (Cognitive Neuroscience, Neuroscience), according to OpenAlex
Citations: not cited yet (Europe PMC); 117 references in the paper

Abstract

The integration of synaptic inputs is a fundamental function of neurons. In the traditional model, excitatory inputs are summed at the soma to generate action potentials. However, how synaptic inputs are integrated by dendrites in vivo remains poorly explored. We used intravital two-photon dendritic imaging with a genetically encoded voltage indicator (accelerated sensor of action potentials 5) together with somatic whole-cell patch clamp recordings to investigate how synaptic depolarizations are transferred to the soma in pyramidal neurons of the mouse somatosensory cortex. We studied the integration of synaptic inputs under spontaneous and sensory-evoked conditions, as well as following electrical and optogenetic stimulation. In all cases, while multiple inputs evoked measurable depolarizations in the cell body, isolated synaptic potentials were strongly attenuated. Our results suggest that isolated synaptic inputs have a minimal contribution to somatic depolarization, whereas coincident inputs within short temporal windows are more effective, indicating a regime of dendritic integration that favors coincident or clustered neuronal activity in cortical networks.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

No file of the authors' code could be read here: it is described below, and read at its source.

NTCColumbia

License: none: the authors keep all their rights
State: the link answers, verified on 27 September 2026
Evidence: the link answers
Software Heritage: not checked
Found in: “Data, code, and materials availability:”
Not found: README, license file, CITATION.cff, environment file, tests, continuous integration, documentation
Availability: 1 check, the latest on 27 September 2026: the link answers (HTTP 200)
  • 27 September 2026: the link answers (HTTP 200)

The paper's code and data availability statement is in the Data section.

Tracing map

Proposed by the machine: these links were found in the paper and verified at the source, without human review. The map will receive a Zenodo DOI once one of the paper's authors has validated it with their ORCID.

What the map holds:

  • 1 repository of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
  • 0 scripts, each with its path and the digest of its content;
  • no match between paragraphs and code yet;
  • neither the text of the paper nor the code itself.

Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.

Data

No dataset and no data link were found in the paper.

Data, code, and materials availability

All data needed to evaluate the conclusions in the paper are present in the paper and/or the Supplementary Materials. Plasmids generated in this study can be provided by Addgene (www.addgene.org/; plasmids #224137 and #224136). All original code and analysis have been deposited at Columbia Academic Commons https://doi.org/10.7916/h0hk-kp30 and Columbia University Neurotechnology Center’s GitHub page https://github.com/NTCColumbia/.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 7 authors, 11 MeSH terms, 6 funders, 114 references.

Cite

This paper

Cornejo, V. H., Bouazza-Arostegui, B., Alejandre-Garcia, T., Hao, Y., Lee, S., Lin, M. Z., & Yuste, R. (2026). Highly attenuated dendritic propagation of isolated synaptic potentials in vivo. Science advances, 12(33), eadz4123. https://doi.org/10.1126/sciadv.adz4123

BibTeX

@article{cornejo2026highly,
author = {Cornejo, Victor Hugo and Bouazza-Arostegui, Boris and Alejandre-Garcia, Tzitzitlini and Hao, Yukun and Lee, Sungmoo and Lin, Michael Z. and Yuste, Rafael},
title = {{Highly attenuated dendritic propagation of isolated synaptic potentials in vivo}},
journal = {Science advances},
year = {2026},
month = aug,
volume = {12},
number = {33},
pages = {eadz4123},
publisher = {American Association for the Advancement of Science},
issn = {2375-2548},
doi = {10.1126/sciadv.adz4123},
url = {https://doi.org/10.1126/sciadv.adz4123},
pmid = {42600022},
pmcid = {PMC13475487}
}

RIS

TY - JOUR
AU - Cornejo, Victor Hugo
AU - Bouazza-Arostegui, Boris
AU - Alejandre-Garcia, Tzitzitlini
AU - Hao, Yukun
AU - Lee, Sungmoo
AU - Lin, Michael Z.
AU - Yuste, Rafael
TI - Highly attenuated dendritic propagation of isolated synaptic potentials in vivo
T2 - Science advances
J2 - Sci Adv
PY - 2026
DA - 2026/08/14
VL - 12
IS - 33
SP - eadz4123
SN - 2375-2548
PB - American Association for the Advancement of Science
DO - 10.1126/sciadv.adz4123
UR - https://doi.org/10.1126/sciadv.adz4123
LA - en
ER -

CSL-JSON

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