Evidence map›Paper›PMID 27896432›Full record

ArticleEuropean archives of psychiatry and clinical neuroscience2017

Repression of telomere-associated genes by microglia activation in neuropsychiatric disease.

Golo Kronenberg, Ria Uhlemann, Johanna Schöner, Stephanie Wegner, Valérie Boujon, Nikolas Deigendesch, Matthias Endres, Karen Gertz

Open access · hybridAbstract read
In one paragraph

Article in European archives of psychiatry and clinical neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Microglia and Brain Disorders: The Role of Vitamin D and Its Receptor.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Microglia and Aging: The Role of the TREM2-DAP12 and CX3CL1-CX3CR1 Axes.International journal of molecular sciences · 2018
    Review
  9. Expression ofFrontiers in cellular neuroscience · 2018
    Article
  10. The Emerging Roles for Telomerase in the Central Nervous System.Frontiers in molecular neuroscience · 2018
    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

8 authors at 2 institutions in 1 country.

Golo KronenbergKlinik für Psychiatrie und Psychotherapie, Charité Campus Mitte, Berlin, Germany.
Ria UhlemannCenter for Stroke Research Berlin (CSB), Charité - Universitätsmedizin, Berlin, Germany.
Johanna SchönerKlinik für Psychiatrie und Psychotherapie, Charité Campus Mitte, Berlin, Germany.
Stephanie WegnerCenter for Stroke Research Berlin (CSB), Charité - Universitätsmedizin, Berlin, Germany.
Valérie BoujonCenter for Stroke Research Berlin (CSB), Charité - Universitätsmedizin, Berlin, Germany.
Nikolas DeigendeschInstitut für Neuropathologie, Charité - Universitätsmedizin, Berlin, Germany.
Matthias EndresCenter for Stroke Research Berlin (CSB), Charité - Universitätsmedizin, Berlin, Germany.
Karen GertzCenter for Stroke Research Berlin (CSB), Charité - Universitätsmedizin, Berlin, Germany. karen.gertz@charite.de.
Charité - Universitätsmedizin Berlin · DEGerman Centre for Cardiovascular Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microglia senescence may promote neuropsychiatric disease. This prompted us to examine the relationship between microglia activation states and telomere biology. A panel of candidate genes associated with telomere maintenance, mitochondrial biogenesis, and cell-cycle regulation were investigated in M1- and M2-polarized microglia in vitro as well as in MACS-purified CD11b+ microglia/brain macrophages from models of stroke, Alzheimer's disease, and chronic stress. M1 polarization, ischemia, and Alzheimer pathology elicited a strikingly similar transcriptomic profile with, in particular, reduced expression of murine Tert. Our results link classical microglia activation with repression of telomere-associated genes, suggesting a new mechanism underlying microglia dysfunction.

Indexed as

AnimalsCD11b AntigenCell PolarityCells, CulturedCyclin-Dependent Kinase Inhibitor p21CytokinesDisease Models, AnimalGene Expression RegulationInfarction, Middle Cerebral ArteryLipopolysaccharidesMaleMiceMice, Inbred C57BLMice, TransgenicMicrogliaMutationCD11b AntigenCyclin-Dependent Kinase Inhibitor p21CytokinesLipopolysaccharidesNF-E2-Related Factor 2Presenilin-1RNA, MessengerTelomeraseTert protein, mouseAlzheimer’s diseaseMicrogliaMitochondrial biogenesisNeurodegenerative diseaseTelomerase

Identifiers

PMID27896432
PMCPMC5509772
OpenAlexW2557429398

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.