Evidence map›Paper›PMID 25384983›Full record

ArticleThe Journal of biological chemistry2014

Carbon monoxide (CO) is a novel inhibitor of connexin hemichannels.

Carmen G León-Paravic, Vania A Figueroa, Diego J Guzmán, Carlos F Valderrama, Antonio A Vallejos, Mariana C Fiori, Guillermo A Altenberg, Luis Reuss, Mauricio A Retamal

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Extracellular Cysteines Are Critical to Form Functional Cx46 Hemichannels.International journal of molecular sciences · 2022
    Article
  7. Review
  8. [Carbon Monoxide and Pain Regulation: A Review].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2021
    Review
  9. Review
  10. Connexins-Therapeutic Targets in Cancers.International journal of molecular sciences · 2020
    Review
  11. Role of ROS/RNS in Preeclampsia: Are Connexins the Missing Piece?International journal of molecular sciences · 2020
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
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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 at 4 institutions in 2 countries.

Carmen G León-ParavicFrom the Centro de Fisiología Celular e Integrativa, Facultad de Medicina, Clínica Alemana Universidad del Desarrollo, Santiago, Chile 7690000 and.
Vania A FigueroaFrom the Centro de Fisiología Celular e Integrativa, Facultad de Medicina, Clínica Alemana Universidad del Desarrollo, Santiago, Chile 7690000 and.
Diego J GuzmánFrom the Centro de Fisiología Celular e Integrativa, Facultad de Medicina, Clínica Alemana Universidad del Desarrollo, Santiago, Chile 7690000 and.
Carlos F ValderramaFrom the Centro de Fisiología Celular e Integrativa, Facultad de Medicina, Clínica Alemana Universidad del Desarrollo, Santiago, Chile 7690000 and.
Antonio A VallejosFrom the Centro de Fisiología Celular e Integrativa, Facultad de Medicina, Clínica Alemana Universidad del Desarrollo, Santiago, Chile 7690000 and.
Mariana C Fiorithe Department of Cell Physiology and Molecular Biophysics, and Center for Membrane Protein Research, Texas Tech University Health Sciences Center, Lubbock, Texas 79430.
Guillermo A Altenbergthe Department of Cell Physiology and Molecular Biophysics, and Center for Membrane Protein Research, Texas Tech University Health Sciences Center, Lubbock, Texas 79430.
Luis Reussthe Department of Cell Physiology and Molecular Biophysics, and Center for Membrane Protein Research, Texas Tech University Health Sciences Center, Lubbock, Texas 79430.
Mauricio A RetamalFrom the Centro de Fisiología Celular e Integrativa, Facultad de Medicina, Clínica Alemana Universidad del Desarrollo, Santiago, Chile 7690000 and the Department of Cell Physiology and Molecular Biophysics, and Center for Membrane Protein Research, Texas Tech University Health Sciences Center, Lubbock, Texas 79430 mretamal@udd.cl.
Texas Tech University · USUniversidad del Desarrollo · CLClínica Alemana · CLTexas Tech University Health Sciences Center · US

Funding

Architecture of the transmembrane pore formed by connexin 43R01GM079629 · NIGMS · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI ALTENBERG, GUILLERMO A · 2007 to 2011
$1.7M
NIGMS NIH HHS 3R01GM079629-03S1NIGMS NIH HHS R01 GM079629NIGMS NIH HHS R01GM79629 AND
6 · The paper itself

Abstract

Hemichannels (HCs) are hexamers of connexins that can form gap-junction channels at points of cell contacts or "free HCs" at non-contacting regions. HCs are involved in paracrine and autocrine cell signaling, and under pathological conditions may induce and/or accelerate cell death. Therefore, studies of HC regulation are of great significance. Nitric oxide affects the activity of Cx43 and Cx46 HCs, whereas carbon monoxide (CO), another gaseous transmitter, modulates the activity of several ion channels, but its effect on HCs has not been explored. We studied the effect of CO donors (CORMs) on Cx46 HCs expressed in Xenopus laevis oocytes using two-electrode voltage clamp and on Cx43 and Cx46 expressed in HeLa cells using a dye-uptake technique. CORM-2 inhibited Cx46 HC currents in a concentration-dependent manner. The C-terminal domain and intracellular Cys were not necessary for the inhibition. The effect of CORM-2 was not prevented by guanylyl-cyclase, protein kinase G, or thioredoxin inhibitors, and was not due to endocytosis of HCs. However, the effect of CORM-2 was reversed by reducing agents that act extracellularly. Additionally, CO inhibited dye uptake of HeLa cells expressing Cx43 or Cx46, and MCF-7 cells, which endogenously express Cx43 and Cx46. Because CORM-2 carbonylates Cx46 in vitro and induces conformational changes, a direct effect of that CO on Cx46 is possible. The inhibition of HCs could help to understand some of the biological actions of CO in physiological and pathological conditions.

Indexed as

AnimalsCarbon MonoxideConnexin 43ConnexinsGlutathioneHeLa CellsHumansMCF-7 CellsMembrane PotentialsOrganometallic CompoundsProtein CarbonylationReducing AgentsXenopus laevisCarbon MonoxideConnexin 43ConnexinsGJA3 protein, humanGlutathioneOrganometallic CompoundsReducing Agentstricarbonyldichlororuthenium (II) dimerCarbon MonoxideCarbonylationConnexinHemichannelsIon ChannelPost-translational Modification (PTM)Redox Signaling

Identifiers

PMID25384983
PMCPMC4276878
OpenAlexW2056962578

What OpenQuestion holds

Textmetadata
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.