Evidence map›Paper›PMID 33669857›Full record

ArticleInternational journal of molecular sciences2021

Potassium Channels Kv1.3 and Kir2.1 But Not Kv1.5 Contribute to BV2 Cell Line and Primary Microglial Migration.

Ruxandra Anton, Mihail Ghenghea, Violeta Ristoiu, Christophe Gattlen, Marc-Rene Suter, Petre Alexandru Cojocaru, Aurel Popa-Wagner, Bogdan Catalin, Alexandru-Florian Deftu

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–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

15 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Functional Potassium Channels in Macrophages.The Journal of membrane biology · 2023
    Review
  6. Roles of CaBiochemistry and biophysics reports · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Acute liver damage generates age independent microglia morphology changes in mice.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

9 authors.

Ruxandra AntonDepartment of Anatomy, Animal Physiology and Biophysics, Faculty of Biology, University of Bucharest, 050095 București, Romania.
Mihail GhengheaDepartment of Anatomy, Animal Physiology and Biophysics, Faculty of Biology, University of Bucharest, 050095 București, Romania.
Violeta RistoiuDepartment of Anatomy, Animal Physiology and Biophysics, Faculty of Biology, University of Bucharest, 050095 București, Romania.
Christophe GattlenPain Center, Department of Anesthesiology, Lausanne University Hospital (CHUV) and Faculty of Biology and Medicine (FBM), University of Lausanne (UNIL), 1011 Lausanne, Switzerland.ORCID 0000-0002-3223-8721
Marc-Rene SuterPain Center, Department of Anesthesiology, Lausanne University Hospital (CHUV) and Faculty of Biology and Medicine (FBM), University of Lausanne (UNIL), 1011 Lausanne, Switzerland.ORCID 0000-0002-4653-0512
Petre Alexandru CojocaruDepartment of Physiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.ORCID 0000-0003-0794-8358
Aurel Popa-WagnerExperimental Research Center for Normal and Pathological Aging, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.
Bogdan CatalinDepartment of Physiology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania.ORCID 0000-0002-5706-8722
Alexandru-Florian DeftuDepartment of Anatomy, Animal Physiology and Biophysics, Faculty of Biology, University of Bucharest, 050095 București, Romania.ORCID 0000-0002-2556-393X

Funding

Consiliului National al Cercetarii Stiintifice din Invatamantul Superior NFIS-FDI-2019-0741The Research Institute of the University of Bucharest 28543/2017
6 · The paper itself

Abstract

(1) Background: As membrane channels contribute to different cell functions, understanding the underlying mechanisms becomes extremely important. A large number of neuronal channels have been investigated, however, less studied are the channels expressed in the glia population, particularly in microglia. In the present study, we focused on the function of the Kv1.3, Kv1.5 and Kir2.1 potassium channels expressed in both BV2 cells and primary microglia cultures, which may impact the cellular migration process. (2) Methods: Using an immunocytochemical approach, we were able to show the presence of the investigated channels in BV2 microglial cells, record their currents using a patch clamp and their role in cell migration using the scratch assay. The migration of the primary microglial cells in culture was assessed using cell culture inserts. (3) Results: By blocking each potassium channel, we showed that Kv1.3 and Kir2.1 but not Kv1.5 are essential for BV2 cell migration. Further, primary microglial cultures were obtained from a line of transgenic CX3CR1-eGFP mice that express fluorescent labeled microglia. The mice were subjected to a spared nerve injury model of pain and we found that microglia motility in an 8 µm insert was reduced 2 days after spared nerve injury (SNI) compared with sham conditions. Additional investigations showed a further impact on cell motility by specifically blocking Kv1.3 and Kir2.1 but not Kv1.5; (4) Conclusions: Our study highlights the importance of the Kv1.3 and Kir2.1 but not Kv1.5 potassium channels on microglia migration both in BV2 and primary cell cultures.

Indexed as

Cell MovementAnimalsCell LineElectrophysiological PhenomenaKv1.3 Potassium ChannelKv1.5 Potassium ChannelMice, TransgenicMicrogliaNerve TissuePotassium Channels, Inwardly RectifyingKir2.1 channelKv1.3 Potassium ChannelKv1.5 Potassium ChannelPotassium Channels, Inwardly Rectifyingmicroglial cellsmigrationpainpotassium channelsspared nerve injury

Identifiers

PMID33669857
PMCPMC7923211

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.