Evidence map›Paper›PMID 42239315›Full record

ArticlebioRxiv : the preprint server for biology2026

Temporal cortex astrocytic Gi-GPCR signaling regulates learned threat responses.

Salome Nora Heimbach, Álvaro Collazos Matute, Victoria Steininger, Reuben Rajadhyaksha, Lea Klein, Lily Ferguson, Yaseer A Sabir, Mingxia Huang, Alberto Cruz-Martín, Sarah Melzer

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Salome Nora HeimbachDivision of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.ORCID 0009-0003-0560-6191
Álvaro Collazos MatuteDivision of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Victoria SteiningerDivision of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Reuben RajadhyakshaDivision of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Lea KleinDivision of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Lily FergusonDepartment of Anesthesiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Yaseer A SabirDepartment of Anesthesiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Mingxia HuangDepartment of Anesthesiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Alberto Cruz-MartínDepartment of Anesthesiology, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.
Sarah MelzerDivision of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-6028-9764

Funding

Neurovascular unit dysfunction in Down syndrome revealed by TBIRF1NS128739 · NINDS · UNIVERSITY OF COLORADO DENVER · PI HUANG, MINGXIA, POTTER, HUNTINGTON · 2022 to 2022
$2.6M
Functional heterogeneity of vasoactive intestinal peptide-expressing interneurons in the anterior cingulate cortex R01MH129732 · NIMH · UNIVERSITY OF COLORADO DENVER · PI Alberto Cruz-Martin · 2022 to 2026
$2.0M
Neurovascular unit dysfunction in Down syndrome revealed by TBIR01NS128739 · NINDS · UNIVERSITY OF COLORADO DENVER · PI MINGXIA HUANG, Huntington Potter · 2025 to 2026
$1.5M
NIMH NIH HHS R01 MH129732NINDS NIH HHS R01 NS128739NINDS NIH HHS RF1 NS128739
6 · The paper itself

Abstract

Astrocytes are increasingly recognized as dynamic modulators of brain circuit function, memory processing, and behavior. Emerging evidence suggests that astrocytic G-protein-coupled receptors (GPCRs) are key regulators of these processes through their influence on intracellular signaling and neuron-glia interactions. Here, we show that the repertoire of functionally expressed GPCRs in cortical astrocytes is broader than previously appreciated. Yet, how distinct GPCR pathways contribute to behavioral regulation remains unknown for most brain areas and behavioral contexts. We therefore investigated the role of astrocytic GPCR signaling in the temporal cortex, a region that integrates multimodal sensory information and learned fear associations. Using chemogenetic tools to selectively activate distinct GPCR pathways in astrocytes, we demonstrate that Gi-coupled GPCR signaling, but not Gs- or Gq-coupled signaling, enhances fear memory retrieval.

Identifiers

PMID42239315
PMCPMC13228300

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.