Cited by 221Neuroscience and Neuropharmacology ResearchNeuroinflammation and Neurodegeneration MechanismsNeural dynamics and brain function

The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index; none of the 25 sources its claims cite is checked for support yet.

Rapid Astrocyte Calcium Signals Correlate with Neuronal Activity and Onset of the Hemodynamic Response In Vivo

Open access
Winship, I. R., Plaa, N., Murphy, T. H.·2007·Journal of Neuroscience

Abstract

Elevation of intracellular Ca2+ in astrocytes can influence cerebral microcirculation and modulate synaptic transmission. Recently, in vivo imaging studies identified delayed, sensory-driven Ca2+ oscillations in cortical astrocytes; however, the long latencies of these Ca2+ signals raises questions in regards to their suitability for a role in short-latency modulation of cerebral microcirculation or rapid astrocyte-to-neuron communication. Here, using in vivo two-photon Ca2+ imaging, we demonstrate that approximately 5% of sulforhodamine 101-labeled astrocytes in the hindlimb area of the mouse primary somatosensory cortex exhibit short-latency (peak amplitude approximately 0.5 s after stimulus onset), contralateral hindlimb-selective sensory-evoked Ca2+ signals that operate on a time scale similar to neuronal activity and correlate with the onset of the hemodynamic response as measured by intrinsic signal imaging. The kinetics of astrocyte Ca2+ transients were similar in rise and decay times to postsynaptic neuronal transients, but decayed more slowly than neuropil Ca2+ transients that presumably reflect presynaptic transients. These in vivo findings suggest that astrocytes can respond to sensory activity in a selective manner and process information on a subsecond time scale, enabling them to potentially form an active partnership with neurons for rapid regulation of microvascular tone and neuron-astrocyte network properties.

Overview

AI snapshot

Written from the paper’s full text.

TL;DR

In urethane-anesthetized mice, a small subset (~5%) of SR101-labeled astrocytes in hindlimb somatosensory cortex showed contralateral hindlimb-selective sensory-evoked Ca²⁺ signals peaking ~0.5 s after stimulus onset. These rapid astrocyte signals matched neuronal timescales and correlated with the onset of the hemodynamic response, suggesting astrocytes can respond on subsecond timescales relevant to neurovascular coupling.

Key findings

  • Of 355 astrocytes (7 mice), 18 (5.07%; 5.08 ± 1.28% per mouse) showed above-threshold Ca²⁺ elevation after contralateral hindlimb stimulation; no other limbs induced significant responses. Astrocyte peak amplitude was 19.1 ± 1.7% ΔF/F₀.
  • Time-to-peak did not differ significantly among astrocytes (0.41 ± 0.11 s), neurons (0.56 ± 0.09 s), and neuropil (0.43 ± 0.09 s; F(2,18) = 0.67; p = 0.52). Decay tau was shorter in neuropil (0.55 ± 0.04 s) than astrocytes (1.07 ± 0.17 s; p = 0.011) and neurons (1.21 ± 0.18 s; p = 0.005).
  • The IOS hemodynamic response began ~600–800 ms after stimulus onset, while astrocyte Ca²⁺ peaked ~0.5 s after onset. Endfoot transients occurred in 12.7% of endfeet (n = 102; 4 mice), with peak 18.8 ± 5.4%, time-to-peak 0.73 ± 0.19 s, and decay tau 0.93 ± 0.10 s.
  • Astrocyte responses were unlikely to be neuropil contamination: mean absolute OGB-1 fluorescence increase was 44.4 ± 5.1 gray levels in astrocytes vs 13.3 ± 1.4 in neuropil ROIs (t test, p << 0.001).

Methods

  • Urethane-anesthetized C57B6 mice (male and female, 2–4 months). Intrinsic optical signal imaging mapped hindlimb/forelimb cortex during mechanical limb stimulation; two-photon Ca²⁺ imaging used OGB-1 and SR101 in layers I–III of hindlimb somatosensory cortex.
  • 355 astrocytes across 7 mice; stimuli were 0.5–1.0 s at 3, 10, or 100 Hz. Responses were thresholded as ΔF/F₀ >1 SD over baseline for ≥0.5 s; ANOVA with post hoc t tests and Bonferroni correction was used, and G/R ratio controlled for movement artifact in high-resolution endfoot imaging.

Limitations

  • The paper does not present a formal limitations section; it notes significant intertrial variability in endfoot Ca²⁺ responses.
  • Evident from the text: only a small subset of astrocytes responded (~5%; 18 responsive astrocytes), imaging was limited to anesthetized mice and layers I–III of hindlimb cortex, and the study reports correlations with hemodynamic onset rather than causal manipulation of astrocyte Ca²⁺ or blood flow.

Model-written summary. Check it against the paper before relying on it.

Integrity signals

Registry

Crossref · 10.1523/jneurosci.4801-06.2007

Cites

32 of 32 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Verification

Claims the paper makes

0 of 25 cited sources checked · 0 supported · 0 flagged

Show all 20 claims

  • The quote only partly states this claim. 1
  • It may state two separate claims as one. 4
  • Probably not a substantial claim. 4
8 of 8

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

Cites

Flagged first, then by citations

Show all 32 references

Cited by

Sorted by citations

Items 101–200 of 218

Metadata

Authors
Winship, I. R., Plaa, N., & Murphy, T. H.
Affiliations
University of British Columbia (CA)
Venue
Journal of Neuroscience
Published
2007-06-06
Volume
27
Issue
23
Pages
6268-6272
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
OpenAlex
W2054459050
Cited by
221
References
32
Citations by year
2025: 7 · 2024: 4 · 2023: 12 · 2022: 9 · 2021: 11 · 2020: 9 · 2019: 5 · 2018: 8 · 2017: 9 · 2016: 16 · 2015: 17 · 2014: 14 · 2013: 21 · 2012: 19
FWCI
6.34
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Heart and Stroke Foundation of Canada
  • Canadian Stroke Network
  • Michael Smith Health Research BC
  • Canadian Institutes of Health Research
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Keywords
calcium oscillations, sensory evoked potentials, primary somatosensory cortex, hemodynamic response, astrocyte-neuron communication, cerebral microcirculation, sulforhodamine 101, intrinsic signal imaging, microvascular tone, neuronal activity
MeSH terms
Action Potentials, Animals, Astrocytes, Female, Hindlimb, Male, Mice, Inbred C57BL, Microcirculation, Neurons, Somatosensory Cortex, Time Factors, Calcium Signaling, Mice

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

A language model drew the claims from the paper on 2026-10-09, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).

A second model labelled each claim on 2026-10-09 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review