Evidence map›Paper›PMID 30964858›Full record

ArticlePLoS biology2019

Infection-generated electric field in gut epithelium drives bidirectional migration of macrophages.

Yaohui Sun, Brian Reid, Fernando Ferreira, Guillaume Luxardi, Li Ma, Kristen L Lokken, Kan Zhu, Gege Xu, Yuxin Sun, Volodymyr Ryzhuk and 5 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Article
  3. Piezo1 mediates electrotaxis of alveolar epithelial cells via calcium-dependent PI3K/Akt signaling.Chinese journal of traumatology = Zhonghua chuang shang za zhi · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Galvanotactic directionality of cell groups depends on group size.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Article
  10. Dysbiosis and extraintestinal cancers.Journal of experimental & clinical cancer research : CR · 2025
    Review
  11. Article
  12. Article
  13. Reducing Sialylation Enhances Electrotaxis of Corneal Epithelial Cells.International journal of molecular sciences · 2023
    Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  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

15 authors at 3 institutions in 3 countries.

Yaohui SunDepartment of Dermatology, School of Medicine, University of California, Davis, Sacramento, California, United States of America.ORCID 0000-0002-3716-6659
Brian ReidDepartment of Dermatology, School of Medicine, University of California, Davis, Sacramento, California, United States of America.
Fernando FerreiraDepartment of Dermatology, School of Medicine, University of California, Davis, Sacramento, California, United States of America.ORCID 0000-0001-5786-8896
Guillaume LuxardiDepartment of Dermatology, School of Medicine, University of California, Davis, Sacramento, California, United States of America.
Li MaDepartment of Dermatology, School of Medicine, University of California, Davis, Sacramento, California, United States of America.
Kristen L LokkenDepartment of Microbiology and Immunology, School of Medicine, University of California, Davis, Davis, California, United States of America.
Kan ZhuDepartment of Dermatology, School of Medicine, University of California, Davis, Sacramento, California, United States of America.ORCID 0000-0002-1146-8130
Gege XuDepartment of Chemistry, University of California, Davis, Davis, California, United States of America.
Yuxin SunDepartment of Dermatology, School of Medicine, University of California, Davis, Sacramento, California, United States of America.
Volodymyr RyzhukDepartment of Dermatology, School of Medicine, University of California, Davis, Sacramento, California, United States of America.ORCID 0000-0001-6988-3575
Betty P GuoOffice of Research, School of Medicine, University of California, Davis, Davis, California, United States of America.
Carlito B LebrillaDepartment of Chemistry, University of California, Davis, Davis, California, United States of America.
Emanual MaverakisDepartment of Dermatology, School of Medicine, University of California, Davis, Sacramento, California, United States of America.
Alex MogilnerCourant Institute and Department of Biology, New York University, New York, New York, United States of America.
Min ZhaoDepartment of Dermatology, School of Medicine, University of California, Davis, Sacramento, California, United States of America.ORCID 0000-0002-2500-3035
University of California, Davis · USCourant Institute of Mathematical Sciences · USShanghai Skin Disease Hospital · CN

Funding

Investigation and Development of New Therapeutic Avenues for SclerodermaDP2OD008752 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MAVERAKIS, EMANUAL M. · 2011 to 2016
$2.8M
NIH HHS DP2 OD008752
6 · The paper itself

Abstract

Many bacterial pathogens hijack macrophages to egress from the port of entry to the lymphatic drainage and/or bloodstream, causing dissemination of life-threatening infections. However, the underlying mechanisms are not well understood. Here, we report that Salmonella infection generates directional electric fields (EFs) in the follicle-associated epithelium of mouse cecum. In vitro application of an EF, mimicking the infection-generated electric field (IGEF), induces directional migration of primary mouse macrophages to the anode, which is reversed to the cathode upon Salmonella infection. This infection-dependent directional switch is independent of the Salmonella pathogenicity island 1 (SPI-1) type III secretion system. The switch is accompanied by a reduction of sialic acids on glycosylated surface components during phagocytosis of bacteria, which is absent in macrophages challenged by microspheres. Moreover, enzymatic cleavage of terminally exposed sialic acids reduces macrophage surface negativity and severely impairs directional migration of macrophages in response to an EF. Based on these findings, we propose that macrophages are attracted to the site of infection by a combination of chemotaxis and galvanotaxis; after phagocytosis of bacteria, surface electrical properties of the macrophage change, and galvanotaxis directs the cells away from the site of infection.

Indexed as

AnimalsBacterial ProteinsCell MovementElectric ConductivityElectricityEpitheliumFemaleGastrointestinal TractMacrophagesMaleMiceMice, Inbred C57BLPhagocytosisSalmonellaSalmonella InfectionsTaxis ResponseBacterial Proteins

Identifiers

PMID30964858
PMCPMC6456179
OpenAlexW2949521843

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.