Evidence map›Paper›PMID 21606109›Full record

ArticleThe Journal of physiology2011

pH-dependent modulation of connexin-based gap junctional uncouplers.

Vytenis A Skeberdis, Lina Rimkute, Aiste Skeberdyte, Nerijus Paulauskas, Feliksas F Bukauskas

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

22 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Endogenous pannexin1 channels form functional intercellular cell-cell channels with characteristic voltage-dependent properties.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. The mutual interplay of redox signaling and connexins.Journal of molecular medicine (Berlin, Germany) · 2021
    Review
  7. Neuronal Glutamatergic Network Electrically Wired with Silent But Activatable Gap Junctions.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  8. Article
  9. Review
  10. Distinct moieties underlie biphasic HFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  11. Article
  12. Mechanism of action of the anti-inflammatory connexin43 mimetic peptide JM2.American journal of physiology. Cell physiology · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Fast structural responses of gap junction membrane domains to AB5 toxins.Proceedings of the National Academy of Sciences of the United States of America · 2013
    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

5 authors at 2 institutions in 2 countries.

Vytenis A SkeberdisLithuanian University of Health Sciences, Institute of Cardiology, 17 Sukilėliųu Avenue, Kaunas 50009, Lithuania.
Lina Rimkute
Aiste Skeberdyte
Nerijus Paulauskas
Feliksas F Bukauskas
Yeshiva University · USLithuanian University of Health Sciences · LT

Funding

Connexins and Heart FunctionR01HL084464 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BUKAUSKAS, FELIKSAS · 2007 to 2010
$1.7M
Gating of Connexin-Based Gap Junction Channels and HemichannelsR01NS072238 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BUKAUSKAS, FELIKSAS · 2010 to 2013
$1.4M
NHLBI NIH HHS HL084464NHLBI NIH HHS R01 HL084464NINDS NIH HHS NS072238NINDS NIH HHS R01 NS072238
6 · The paper itself

Abstract

Gap junction (GJ) channels formed from connexin (Cx) proteins provide a direct pathway for electrical and metabolic cell–cell communication exhibiting high sensitivity to intracellular pH (pH(i)). We examined pH(i)-dependent modulation of junctional conductance (g(j)) of GJs formed of Cx26, mCx30.2, Cx36, Cx40, Cx43, Cx45, Cx46, Cx47 and Cx50 by reagents representing several distinct groups of uncouplers, such as long carbon chain alkanols (LCCAs), arachidonic acid, carbenoxolone, isoflurane, flufenamic acid and mefloquine. We demonstrate that alkalization by NH4Cl to pH ∼8 increased g(j) in cells expressing mCx30.2 and Cx45, yet did not affect g(j) of Cx26, Cx40, Cx46, Cx47 and Cx50 and decreased it in Cx43 and Cx36 GJs. Unexpectedly, cells expressing Cx45, but not other Cxs, exhibited full coupling recovery after alkalization with NH4Cl under the continuous presence of LCCAs, isoflurane and mefloquine. There was no coupling recovery by alkalization in the presence of arachidonic acid, carbenoxolone and flufenamic acid. In cells expressing Cx45, IC50 for octanol was 0.1, 0.25 and 2.68 mm at pH(i) values of 6.9, 7.2 and 8.1, respectively. Histidine modification of Cx45 protein by N-bromosuccinimide reduced the coupling-promoting effect of NH4Cl as well as the uncoupling effect of octanol. This suggests that LCCAs and some other uncouplers may act through the formation of hydrogen bonds with the as-of-yet unidentified histidine/s of the Cx45 GJ channel protein.

Indexed as

BromosuccinimideCell CommunicationCells, CulturedConnexin 26ConnexinsGap JunctionsHeLa CellsHumansHydrogen BondingHydrogen-Ion ConcentrationOctanolsProtein IsoformsBromosuccinimideConnexin 26ConnexinsGJB2 protein, humanOctanolsProtein Isoforms

Identifiers

PMID21606109
PMCPMC3167113
OpenAlexW1596394209

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.