Evidence map›Paper›PMID 33708355›Full record

ArticleJournal of extracellular vesicles2020

Microglial derived extracellular vesicles activate autophagy and mediate multi-target signaling to maintain cellular homeostasis.

Bram Van den Broek, Isabel Pintelon, Ibrahim Hamad, Sofie Kessels, Mansour Haidar, Niels Hellings, Jerome J A Hendriks, Markus Kleinewietfeld, Bert Brône, Vincent Timmerman and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of extracellular vesicles, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

30 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Ancient Medicinal InsectInternational journal of nanomedicine · 2025
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  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

14 authors at 3 institutions in 1 country.

Bram Van den BroekBiomedical Research Institute UHasselt Hasselt University Hasselt Belgium.ORCID 0000-0003-4624-4812
Isabel PintelonLaboratory of Cell Biology & Histology Antwerp Centre for Advanced Microscopy (ACAM) University of Antwerp Antwerp Belgium.
Ibrahim HamadBiomedical Research Institute UHasselt Hasselt University Hasselt Belgium.
Sofie KesselsBiomedical Research Institute UHasselt Hasselt University Hasselt Belgium.ORCID 0000-0002-0070-7482
Mansour HaidarBiomedical Research Institute UHasselt Hasselt University Hasselt Belgium.
Niels HellingsBiomedical Research Institute UHasselt Hasselt University Hasselt Belgium.
Jerome J A HendriksBiomedical Research Institute UHasselt Hasselt University Hasselt Belgium.
Markus KleinewietfeldBiomedical Research Institute UHasselt Hasselt University Hasselt Belgium.
Bert BrôneBiomedical Research Institute UHasselt Hasselt University Hasselt Belgium.ORCID 0000-0002-4851-9480
Vincent TimmermanPeripheral Neuropathy Research Group Department of Biomedical Sciences Institute Born Bunge and University of Antwerp Antwerp Belgium.ORCID 0000-0002-2162-0933
Jean-Pierre TimmermansLaboratory of Cell Biology & Histology Antwerp Centre for Advanced Microscopy (ACAM) University of Antwerp Antwerp Belgium.
Veerle SomersBiomedical Research Institute UHasselt Hasselt University Hasselt Belgium.
Luc MichielsBiomedical Research Institute UHasselt Hasselt University Hasselt Belgium.
Joy IrobiBiomedical Research Institute UHasselt Hasselt University Hasselt Belgium.ORCID 0000-0001-7300-1520
Hasselt University · BEUniversity of Antwerp · BEVIB-UGent Center for Inflammation Research · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microglia, the immunocompetent cells of the central nervous system (CNS), play an important role in maintaining cellular homeostasis in the CNS. These cells secrete immunomodulatory factors including nanovesicles and participate in the removal of cellular debris by phagocytosis or autophagy. Accumulating evidence indicates that specifically the cellular exchange of small extracellular vesicles (EVs), participates in physiology and disease through intercellular communication. However, the contribution of microglial-derived extracellular vesicles (M-EVs) to the maintenance of microglia homeostasis and how M-EVs could influence the phenotype and gene function of other microglia subtypes is unclear. In addition, knowledge of canonical signalling pathways of inflammation and immunity gene expression patterns in human microglia exposed to M-EVs is limited. Here, we analysed the effects of M-EVs produced in vitro by either tumour necrosis factor alpha (TNFα) activated or non-activated microglia BV2 cells. We showed that M-EVs are internalized by both mouse and human C20 microglia cells and that the uptake of M-EVs in microglia induced autophagic vesicles at various stages of degradation including autophagosomes and autolysosomes. Consistently, stimulation of microglia with M-EVs increased the protein expression of the autophagy marker, microtubule-associated proteins 1A/1B light chain 3B isoform II (LC3B-II), and promoted autophagic flux in live cells. To elucidate the biological activities occurring at the transcriptional level in C20 microglia stimulated with M-EVs, the gene expression profiles, potential upstream regulators, and enrichment pathways were characterized using targeted RNA sequencing. Inflammation and immunity transcriptome gene panel sequencing of both activated and normal microglia stimulated with M-EVs showed involvement of several canonical pathways and reduced expression of key genes involved in neuroinflammation, inflammasome and apoptosis signalling pathways compared to control cells. In this study, we provide the perspective that a beneficial activity of in vitro cell culture produced EVs could be the modulation of autophagy during cellular stress. Therefore, we use a monoculture system to study microglia-microglia crosstalk which is important in the prevention and propagation of inflammation in the brain. We demonstrate that in vitro produced microglial EVs are able to influence multiple biological pathways and promote activation of autophagy in order to maintain microglia survival and homeostasis.

Indexed as

AutophagySignal TransductionAnimalsCell LineExtracellular VesiclesGene Expression RegulationHumansMiceMicrogliaMicrotubule-Associated ProteinsMAP1LC3B protein, humanMap1lc3b protein, mouseMicrotubule-Associated Proteinsautophagycellular homeostasisextracellular vesiclesgene expressionimmunityinflammation genesmicrogliaRNA sequencing

Identifiers

PMID33708355
PMCPMC7890546
OpenAlexW3108559529

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.