Evidence map›Paper›PMID 37845031›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2023

β-Adrenergic Signaling Promotes Morphological Maturation of Astrocytes in Female Mice.

Marci F Rosenberg, Marlesa I Godoy, Sarah D Wade, Mercedes F Paredes, Ye Zhang, Anna V Molofsky

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Crosstalk of noradrenergic CaCell communication and signaling : CCS · 2026
    Article
  2. Article
  3. Article
  4. Wake-promoting neuromodulators in Alzheimer's disease: Implications for sleep and brain clearance.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Review
  5. Review
  6. Development and diversity of astrocytes.Development (Cambridge, England) · 2025
    Review
  7. Article
  8. Review
  9. Review
  10. Astrocyte morphology.Trends in cell biology · 2024
    Review
  11. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Marci F RosenbergDepartment of Psychiatry and Behavioral Sciences and Weill Institute of Neurosciences, University of California at San Francisco, San Francisco, California 94143.
Marlesa I GodoyDepartment of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, California 90095.
Sarah D WadeDepartment of Psychiatry and Behavioral Sciences and Weill Institute of Neurosciences, University of California at San Francisco, San Francisco, California 94143.
Mercedes F ParedesDepartment of Neurology, Weill Institute of Neurosciences, University of California, San Francisco, San Francisco, California 94143.
Ye ZhangDepartment of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, University of California, Los Angeles, California 90095.
Anna V MolofskyDepartment of Psychiatry and Behavioral Sciences and Weill Institute of Neurosciences, University of California at San Francisco, San Francisco, California 94143 anna.molofsky@ucsf.edu.ORCID 0000-0002-4709-2411
University of California, San Francisco · USUniversity of California, Los Angeles · US

Funding

Regulation of Cellular Pathwaysin Human Brain DevelopmentP01NS083513 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRIEGSTEIN, ARNOLD · 2014 to 2024
$12.6M
Predoctoral Training in NeurobiologyT32NS115706 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SAMUEL JEREMY PLEASURE · 2020 to 2026
$3.4M
Microglial remodeling of the extracellular matrix in memory circuitsR01MH125000 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MOLOFSKY, ANNA V · 2021 to 2025
$3.3M
Gyrencephalic Model for Neurodevelopmental Disease and Postnatal Cortical Therapeutic InterventionsDP2NS122550 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PAREDES, MERCEDES · 2020 to 2020
$2.4M
Training Grant in Neurobehavioral GeneticsT32MH073526 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BEARDEN, CARRIE E, GESCHWIND, DANIEL H · 2006 to 2020
$2.4M
Astrocyte-microglial communication in developmental synapse formationR01MH119349 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MOLOFSKY, ANNA V · 2019 to 2023
$2.0M
Molecular characterization of reactive astrocytes in humansR01NS109025 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ZHANG, YE · 2018 to 2022
$1.7M
Noradrenergic regulation of grey-matter astrocyte maturationF30MH124367 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSENBERG, MARCI · 2020 to 2023
$181k
NIMH NIH HHS F30 MH124367NIMH NIH HHS R01 MH119349NIMH NIH HHS R01 MH125000NIMH NIH HHS T32 MH073526NINDS NIH HHS DP2 NS122550NINDS NIH HHS P01 NS083513NINDS NIH HHS R01 NS109025NINDS NIH HHS T32 NS115706
6 · The paper itself

Abstract

Astrocytes play essential roles in the developing nervous system, including supporting synapse function. These astrocyte support functions emerge coincident with brain maturation and may be tailored in a region-specific manner. For example, gray matter astrocytes have elaborate synapse-associated processes and are morphologically and molecularly distinct from white matter astrocytes. This raises the question of whether there are unique environmental cues that promote gray matter astrocyte identity and synaptogenic function. We previously identified adrenergic receptors as preferentially enriched in developing gray versus white matter astrocytes, suggesting that noradrenergic signaling could be a cue that promotes the functional maturation of gray matter astrocytes. We first characterized noradrenergic projections during postnatal brain development in mouse and human, finding that process density was higher in the gray matter and increased concurrently with astrocyte maturation. RNA sequencing revealed that astrocytes in both species expressed α- and β-adrenergic receptors. We found that stimulation of β-adrenergic receptors increased primary branching of rodent astrocytes

Indexed as

Adrenergic AgentsAstrocytesAnimalsFemaleHumansMiceNorepinephrineReceptors, AdrenergicReceptors, Adrenergic, betaSignal TransductionAdrenergic AgentsNorepinephrineReceptors, AdrenergicReceptors, Adrenergic, betaastrocytebrain developmentnorepinephrineβ-adrenergic receptor

Identifiers

PMID37845031
PMCPMC10727121
OpenAlexW4387665801

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.