Evidence map›Paper›PMID 29046334›Full record

ArticleThe EMBO journal2017

The organic anion transporter SLCO2A1 constitutes the core component of the Maxi-Cl channel.

Ravshan Z Sabirov, Petr G Merzlyak, Toshiaki Okada, Md Rafiqul Islam, Hiromi Uramoto, Tomoko Mori, Yumiko Makino, Hiroshi Matsuura, Yu Xie, Yasunobu Okada

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
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  5. Molecular basis of prostaglandin ENature communications · 2025
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  9. Pathogenesis of chronic enteropathy associated with theWorld journal of gastroenterology · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. ATP Synthase KFunction (Oxford, England) · 2022
    Article
  16. Review
  17. Review
  18. Positive Inotropic Effects of ATP ReleasedFrontiers in cell and developmental biology · 2021
    Article
  19. Glial Chloride Channels in the Function of the Nervous System Across Species.Advances in experimental medicine and biology · 2021
    Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 2 countries.

Ravshan Z SabirovInternational Collaborative Research Project, National Institute for Physiological Sciences, Okazaki, Japan.
Petr G MerzlyakInternational Collaborative Research Project, National Institute for Physiological Sciences, Okazaki, Japan.
Toshiaki OkadaInternational Collaborative Research Project, National Institute for Physiological Sciences, Okazaki, Japan.ORCID 0000-0001-9145-1429
Md Rafiqul IslamInternational Collaborative Research Project, National Institute for Physiological Sciences, Okazaki, Japan.
Hiromi UramotoDepartment of Health and Nutrition, Jin-ai University, Echizen, Japan.
Tomoko MoriCore Research Facilities, National Institute for Basic Biology, Okazaki, Japan.
Yumiko MakinoCore Research Facilities, National Institute for Basic Biology, Okazaki, Japan.
Hiroshi MatsuuraDepartment of Physiology, Shiga University of Medical Science, Otsu, Japan.
Yu XieDepartment of Physiology, Shiga University of Medical Science, Otsu, Japan.
Yasunobu OkadaInternational Collaborative Research Project, National Institute for Physiological Sciences, Okazaki, Japan okada@nips.ac.jp.ORCID 0000-0003-0899-1665
Academy of Sciences Republic of Uzbekistan · UZNational Institute for Basic Biology · JPNational Institute for Physiological Sciences · JPShiga University of Medical Science · JPJin-ai University · JPThe Graduate University for Advanced Studies, SOKENDAI · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The maxi-anion channels (MACs) are expressed in cells from mammals to amphibians with ~60% exhibiting a phenotype called Maxi-Cl. Maxi-Cl serves as the most efficient pathway for regulated fluxes of inorganic and organic anions including ATP However, its molecular entity has long been elusive. By subjecting proteins isolated from bleb membranes rich in Maxi-Cl activity to LC-MS/MS combined with targeted siRNA screening, CRISPR/Cas9-mediated knockout, and heterologous overexpression, we identified the organic anion transporter SLCO2A1, known as a prostaglandin transporter (PGT), as a key component of Maxi-Cl. Recombinant SLCO2A1 exhibited Maxi-Cl activity in reconstituted proteoliposomes. When SLCO2A1, but not its two disease-causing mutants, was heterologously expressed in cells which lack endogenous SLCO2A1 expression and Maxi-Cl activity, Maxi-Cl currents became activated. The charge-neutralized mutant became weakly cation-selective with exhibiting a smaller single-channel conductance.

Indexed as

Adenosine TriphosphateAnimalsCell FractionationCell MembraneCRISPR-Cas SystemsDinoprostoneFemaleGene DeletionGene SilencingGreen Fluorescent ProteinsHEK293 CellsHumansIon Channel GatingIon ChannelsMembrane ProteinsMice, Inbred C57BLAdenosine TriphosphateDinoprostoneGreen Fluorescent ProteinsIon ChannelsMembrane ProteinsOrganic Anion TransportersProteolipidsproteoliposomesRecombinant ProteinsSlco2a1 protein, mouseanion channelMaxi‐Clmolecular entityorganic anion transporterSLCO2A1

Identifiers

PMID29046334
PMCPMC5686547
OpenAlexW2766505448

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.