Evidence map›Paper›PMID 39207536›Full record

ArticleActa neuropathologica2024

PRDM16-DT is a novel lncRNA that regulates astrocyte function in Alzheimer's disease.

Sophie Schröder, Ulrike Fuchs, Verena Gisa, Tonatiuh Pena, Dennis M Krüger, Nina Hempel, Susanne Burkhardt, Gabriela Salinas, Anna-Lena Schütz, Ivana Delalle and 2 more

Abstract read
In one paragraph

Article in Acta neuropathologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
–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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. ThebioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. TREK1 Channels Shape Spindle-Like Oscillations, Neuronal Activity, and Short-Term Synaptic Plasticity in Thalamocortical Circuits.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  10. lncRNAbioRxiv : the preprint server for biology · 2025
    Article
  11. Article
  12. LncRNANon-coding RNA · 2025
    Article
  13. 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

12 authors.

Sophie SchröderDepartment for Systems Medicine and Epigenetics, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Ulrike FuchsDepartment for Systems Medicine and Epigenetics, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Verena GisaDepartment for Systems Medicine and Epigenetics, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Tonatiuh PenaDepartment for Systems Medicine and Epigenetics, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Dennis M KrügerDepartment for Systems Medicine and Epigenetics, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Nina HempelDepartment for Systems Medicine and Epigenetics, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Susanne BurkhardtDepartment for Systems Medicine and Epigenetics, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany.
Gabriela SalinasNGS- Integrative Genomics Core Unit, Institute of Pathology, University Medical Center, Göttingen, Germany.
Anna-Lena SchützResearch Group for Genome Dynamics in Brain Diseases, German Center for Neurodegenerative Diseases, Göttingen, Germany.
Ivana DelalleDepartment of Pathology and Laboratory Medicine, Boston University School of Medicine, 670 Albany Street, Boston, MA, 02118, USA.
Farahnaz SananbenesiResearch Group for Genome Dynamics in Brain Diseases, German Center for Neurodegenerative Diseases, Göttingen, Germany.
Andre FischerDepartment for Systems Medicine and Epigenetics, German Center for Neurodegenerative Diseases (DZNE), Göttingen, Germany. afische2@gwdg.de.ORCID 0000-0001-8546-1161

Funding

Research Education CoreP30AG066462 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PHILIP L DE JAGER · 2020 to 2026
$30.1M
MicroRNAs as Diagnostic and Prognostic Biomarker of Alzheimer's DiseaseRF1AG078299 · NIA · RHODE ISLAND HOSPITAL · PI BLUSZTAJN, JAN KRZYSZTOF, DELALLE, IVANA · 2022 to 2022
$2.4M
Long Non-coding RNAs as Therapeutic Targets and Biomarkers of Alzheimer's Disease and Related DementiasR01AG084624 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI JAN Krzysztof BLUSZTAJN, IVANA DELALLE · 2024 to 2026
$2.3M
Deutsche Forschungsgemeinschaft 1738Deutsche Forschungsgemeinschaft GRK2824;EXC 2067/1 390729940Deutsche Forschungsgemeinschaft SFB1286NIA NIH HHS P30 AG066462NIA NIH HHS R01 AG084624NIA NIH HHS RF1 AG078299
6 · The paper itself

Abstract

Astrocytes provide crucial support for neurons, contributing to synaptogenesis, synaptic maintenance, and neurotransmitter recycling. Under pathological conditions, deregulation of astrocytes contributes to neurodegenerative diseases such as Alzheimer's disease (AD). While most research in this field has focused on protein-coding genes, non-coding RNAs, particularly long non-coding RNAs (lncRNAs), have emerged as significant regulatory molecules. In this study, we identified the lncRNA PRDM16-DT as highly enriched in the human brain, where it is almost exclusively expressed in astrocytes. PRDM16-DT and its murine homolog, Prdm16os, are downregulated in the brains of AD patients and in AD models. In line with this, knockdown of PRDM16-DT and Prdm16os revealed its critical role in maintaining astrocyte homeostasis and supporting neuronal function by regulating genes essential for glutamate uptake, lactate release, and neuronal spine density through interactions with the RE1-Silencing Transcription factor (Rest) and Polycomb Repressive Complex 2 (PRC2). Notably, CRISPR-mediated overexpression of Prdm16os mitigated functional deficits in astrocytes induced by stimuli linked to AD pathogenesis. These findings underscore the importance of PRDM16-DT in astrocyte function and its potential as a novel therapeutic target for neurodegenerative disorders characterized by astrocyte dysfunction.

Indexed as

Alzheimer DiseaseAstrocytesDNA-Binding ProteinsRNA, Long NoncodingTranscription FactorsAnimalsBrainHumansMaleMiceMice, Inbred C57BLNeuronsDNA-Binding ProteinsPRDM16 protein, humanPrdm16 protein, mouseRNA, Long NoncodingTranscription FactorsAlzheimer’s diseaseAstrocyteBrainLong-non-coding RNAPostmortem human brain

Identifiers

PMID39207536
PMCPMC11362476

What OpenQuestion holds

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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.