Evidence map›Paper›PMID 25719758›Full record

ArticlePloS one2015

Regulation of macrophage motility by the water channel aquaporin-1: crucial role of M0/M2 phenotype switch.

Donatienne Tyteca, Tomoya Nishino, Huguette Debaix, Patrick Van Der Smissen, Francisca N'Kuli, Delia Hoffmann, Yvette Cnops, Virginie Rabolli, Geert van Loo, Rudi Beyaert and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Review
  3. Aquaporin-1 and Osmosis: From Physiology to Precision in Peritoneal Dialysis.Journal of the American Society of Nephrology : JASN · 2024
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. The multifaceted role of aquaporins in physiological cell migration.American journal of physiology. Cell physiology · 2023
    Review
  9. Aquaporins in Immune System.Advances in experimental medicine and biology · 2023
    Article
  10. Non-Transport Functions of Aquaporins.Advances in experimental medicine and biology · 2023
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. International journal of molecular sciences · 2020
    Review
  18. Aquaporin 1 alleviates acute kidney injury via PI3K-mediated macrophage M2 polarization.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2020
    Article
  19. Article
  20. Article
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

13 authors at 3 institutions in 2 countries.

Donatienne TytecaCELL Unit, de Duve Institute (DDUV), Université catholique de Louvain, Brussels, Belgium.
Tomoya NishinoPôle de Néphrologie (NEFR), Institut de recherche expérimentale et clinique (IREC), Université catholique de Louvain, Brussels, Belgium; Division of Nephrology, Nagasaki University, Nagasaki, Japan.
Huguette DebaixPôle de Néphrologie (NEFR), Institut de recherche expérimentale et clinique (IREC), Université catholique de Louvain, Brussels, Belgium.
Patrick Van Der SmissenCELL Unit, de Duve Institute (DDUV), Université catholique de Louvain, Brussels, Belgium.
Francisca N'KuliCELL Unit, de Duve Institute (DDUV), Université catholique de Louvain, Brussels, Belgium.
Delia HoffmannCELL Unit, de Duve Institute (DDUV), Université catholique de Louvain, Brussels, Belgium.
Yvette CnopsPôle de Néphrologie (NEFR), Institut de recherche expérimentale et clinique (IREC), Université catholique de Louvain, Brussels, Belgium.
Virginie RabolliLouvain Centre for Toxicology and Applied Pharmacology (LTAP), Institut de recherche expérimentale et clinique (IREC), Université catholique de Louvain, Brussels, Belgium.
Geert van LooInflammation Research Center, VIB, Department of Biomedical Molecular Biology, University of Ghent, Ghent, Belgium.
Rudi BeyaertInflammation Research Center, VIB, Department of Biomedical Molecular Biology, University of Ghent, Ghent, Belgium.
François HuauxLouvain Centre for Toxicology and Applied Pharmacology (LTAP), Institut de recherche expérimentale et clinique (IREC), Université catholique de Louvain, Brussels, Belgium.
Olivier DevuystPôle de Néphrologie (NEFR), Institut de recherche expérimentale et clinique (IREC), Université catholique de Louvain, Brussels, Belgium.
Pierre J CourtoyCELL Unit, de Duve Institute (DDUV), Université catholique de Louvain, Brussels, Belgium.
UCLouvain · BEde Duve Institute · BEVIB-UGent Center for Inflammation Research · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The water channel aquaporin-1 (AQP1) promotes migration of many cell types. Although AQP1 is expressed in macrophages, its potential role in macrophage motility, particularly in relation with phenotype polarization, remains unknown. We here addressed these issues in peritoneal macrophages isolated from AQP1-deficient mice, either undifferentiated (M0) or stimulated with LPS to orientate towards pro-inflammatory phenotype (classical macrophage activation; M1). In non-stimulated macrophages, ablation of AQP1 (like inhibition by HgCl2) increased by 2-3 fold spontaneous migration in a Src/PI3K/Rac-dependent manner. This correlated with cell elongation and formation of lamellipodia/ruffles, resulting in membrane lipid and F4/80 recruitment to the leading edge. This indicated that AQP1 normally suppresses migration of resting macrophages, as opposed to other cell types. Resting Aqp1-/- macrophages exhibited CD206 redistribution into ruffles and increased arginase activity like IL4/IL13 (alternative macrophage activation; M2), indicating a M0-M2 shift. In contrast, upon M1 orientation by LPS in vitro or peritoneal inflammation in vivo, migration of Aqp1-/- macrophages was reduced. Taken together, these data indicate that AQP1 oppositely regulates macrophage migration, depending on stimulation or not by LPS, and that macrophage phenotypic and migratory changes may be regulated independently of external cues.

Indexed as

Cell MovementMacrophage ActivationAnimalsAquaporin 1ArginaseInterleukinsLectins, C-TypeMacrophages, PeritonealMannose-Binding LectinsMannose ReceptorMiceMice, Inbred C57BLPhosphatidylinositol 3-Kinasesrac GTP-Binding ProteinsReceptors, Cell Surfacesrc-Family KinasesAqp1 protein, mouseAquaporin 1ArginaseInterleukinsLectins, C-TypeMannose-Binding LectinsMannose ReceptorPhosphatidylinositol 3-Kinasesrac GTP-Binding ProteinsReceptors, Cell Surfacesrc-Family Kinases

Identifiers

PMID25719758
PMCPMC4342038
OpenAlexW2040831414

What OpenQuestion holds

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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.