Evidence map›Paper›PMID 37155839›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Circadian clock protein BMAL1 broadly influences autophagy and endolysosomal function in astrocytes.

Celia A McKee, Alexander J Polino, Melvin W King, Erik S Musiek

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Observational
  12. REV-ERB-alpha and -beta coordinately regulate astrocyte reactivity and proteostatic function.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  13. Review
  14. Review
  15. Silmitasertib, an FDA-designated orphan CK2 inhibitor, ameliorates neuropathology and motor dysfunction in a Huntington's disease mouse model.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
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

4 authors at 1 institution in 1 country.

Celia A McKeeDepartment of Neurology, Washington University School of Medicine in St. Louis, St. Louis, MO 63110.ORCID 0000-0002-5271-7877
Alexander J PolinoDepartment of Cell Biology and Physiology, Washington University School of Medicine in St. Louis, St. Louis, MO 63110.ORCID 0000-0003-2601-3638
Melvin W KingDepartment of Neurology, Washington University School of Medicine in St. Louis, St. Louis, MO 63110.
Erik S MusiekDepartment of Neurology, Washington University School of Medicine in St. Louis, St. Louis, MO 63110.ORCID 0000-0002-8873-0360
Washington University in St. Louis · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI AIMEE S JAMES · 2001 to 2026
$128.0M
WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
ROLE OF GLIAL CIRCADIAN CLOCK DYSFUNCTION IN THE PATHOGENESIS OF ALZHEIMER'S DISEASER01AG054517 · NIA · WASHINGTON UNIVERSITY · PI Erik Steven Musiek · 2017 to 2026
$4.5M
Sleep and Circadian Rhythms in Alzheimer Disease: Potential bi-directional relationship with tauRF1AG061776 · NIA · WASHINGTON UNIVERSITY · PI HOLTZMAN, DAVID M., JU, YO-EL S · 2019 to 2019
$3.7M
High Sensitivity sCMOS Camera System for Transmission Electron MicroscopeS10OD032186 · OD · WASHINGTON UNIVERSITY · PI PISTON, DAVID W · 2022 to 2022
$147k
NCATS NIH HHS UL1 TR002345NCI NIH HHS P30 CA091842NIA NIH HHS R01 AG054517NIA NIH HHS RF1 AG061776NIH HHS S10 OD032186
6 · The paper itself

Abstract

An emerging role for the circadian clock in autophagy and lysosome function has opened new avenues for exploration in the field of neurodegeneration. The daily rhythms of circadian clock proteins may coordinate gene expression programs involved not only in daily rhythms but in many cellular processes. In the brain, astrocytes are critical for sensing and responding to extracellular cues to support neurons. The core clock protein BMAL1 serves as the primary positive circadian transcriptional regulator and its depletion in astrocytes not only disrupts circadian function but also leads to a unique cell-autonomous activation phenotype. We report here that astrocyte-specific deletion of

Indexed as

Circadian ClocksAnimalsARNTL Transcription FactorsAstrocytesAutophagyCircadian RhythmCLOCK ProteinsLysosomesMiceARNTL Transcription FactorsBmal1 protein, mouseCLOCK ProteinsastrocyteautophagyBmal1circadianlysosome

Identifiers

PMID37155839
PMCPMC10194014
OpenAlexW4375955868

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.