Evidence map›Paper›PMID 22342665›Full record

ReviewBiochimica et biophysica acta2013

Structural basis for the selective permeability of channels made of communicating junction proteins.

Jose F Ek-Vitorin, Janis M Burt

Abstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. The lipidated connexin mimetic peptide SRPTEKT-American journal of physiology. Cell physiology · 2019
    Article
  12. Article
  13. Article
  14. Lipidated connexin mimetic peptides potently inhibit gap junction-mediated CaAmerican journal of physiology. Cell physiology · 2018
    Article
  15. Connexin Communication Compartments and Wound Repair in Epithelial Tissue.International journal of molecular sciences · 2018
    Review
  16. Review
  17. Review
  18. Article
  19. Permeant-specific gating of connexin 30 hemichannels.The Journal of biological chemistry · 2017
    Article
  20. Review
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

2 authors.

Jose F Ek-VitorinDepartment of Physiology, University of Arizona, Tucson, AZ, USA. ekvitori@email.arizona.edu
Janis M Burt

Funding

GAP JUNCTIONS IN VASCULAR SMOOTH MUSCLE--GROWTH CONTROLR01HL058732 · NHLBI · UNIVERSITY OF ARIZONA · PI BURT, JANIS M · 1997 to 2014
$4.2M
Role of Gap Junctions in Blood Vessel AssemblyR01HL077675 · NHLBI · YALE UNIVERSITY · PI BURT, JANIS M, HIRSCHI, KAREN KEMPER · 2004 to 2012
$2.7M
Human Endothelial Cell DifferentiationR01HL096360 · NHLBI · YALE UNIVERSITY · PI HIRSCHI, KAREN KEMPER · 2009 to 2013
$1.5M
NHLBI NIH HHS 5R01HL058732NHLBI NIH HHS 5R01HL077675NHLBI NIH HHS R01 HL058732NHLBI NIH HHS R01 HL077675NHLBI NIH HHS R01 HL096360
6 · The paper itself

Abstract

The open state(s) of gap junction channels is evident from their permeation by small ions in response to an applied intercellular (transjunctional/transchannel) voltage gradient. That an open channel allows variable amounts of current to transit from cell-to-cell in the face of a constant intercellular voltage difference indicates channel open/closing can be complete or partial. The physiological significance of such open state options is, arguably, the main concern of junctional regulation. Because gap junctions are permeable to many substances, it is sensible to inquire whether and how each open state influences the intercellular diffusion of molecules as valuable as, but less readily detected than current-carrying ions. Presumably, structural changes perceived as shifts in channel conductivity would significantly alter the transjunctional diffusion of molecules whose limiting diameter approximates the pore's limiting diameter. Moreover, changes in junctional permeability to some molecules might occur without evident changes in conductivity, either at macroscopic or single channel level. Open gap junction channels allow the exchange of cytoplasmic permeants between contacting cells by simple diffusion. The identity of such permeants, and the functional circumstances and consequences of their junctional exchange presently constitute the most urgent (and demanding) themes of the field. Here, we consider the necessity for regulating this exchange, the possible mechanism(s) and structural elements likely involved in such regulation, and how regulatory phenomena could be perceived as changes in chemical vs. electrical coupling; an overall reflection on our collective knowledge of junctional communication is then applied to suggest new avenues of research. This article is part of a Special Issue entitled: The Communicating junctions, roles and dysfunctions.

Indexed as

AnimalsCell Membrane PermeabilityConnexinsGap JunctionsHumansIon Channel GatingModels, MolecularMutationPhosphorylationProtein ConformationProtein Processing, Post-TranslationalConnexins

Identifiers

PMID22342665
PMCPMC3389294

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.