Evidence map›Paper›PMID 26359298›Full record

ArticleJournal of cell science2015

Two-color fluorescent analysis of connexin 36 turnover: relationship to functional plasticity.

Helen Yanran Wang, Ya-Ping Lin, Cheryl K Mitchell, Sripad Ram, John O'Brien

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

34 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  6. Future avenues inLearning & memory (Cold Spring Harbor, N.Y.) · 2024
    Review
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  12. Altered Expression of GJD2 Messenger RNA and the Coded Protein Connexin 36 in Negative Lens-induced Myopia of Guinea Pigs.Optometry and vision science : official publication of the American Academy of Optometry · 2020
    Article
  13. Article
  14. Article
  15. Endocytosis of Connexin 36 is Mediated by Interaction with Caveolin-1.International journal of molecular sciences · 2020
    Article
  16. 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

5 authors at 2 institutions in 1 country.

Helen Yanran WangRuiz Department of Ophthalmology & Visual Science, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA Graduate School of Biomedical Sciences, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA John.OBrien@uth.tmc.edu Yanran.Wang@uth.tmc.edu.
Ya-Ping LinRuiz Department of Ophthalmology & Visual Science, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Cheryl K MitchellRuiz Department of Ophthalmology & Visual Science, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Sripad RamCarl Zeiss Microscopy LLC, Thornwood, NY 10594, USA.
John O'BrienRuiz Department of Ophthalmology & Visual Science, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA Graduate School of Biomedical Sciences, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA John.OBrien@uth.tmc.edu Yanran.Wang@uth.tmc.edu.
The University of Texas Health Science Center at Houston · USCarl Zeiss (United States) · US

Funding

REGULATION OF RETINAL GAP JUNCTIONSR01EY012857 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI JOHN O'BRIEN · 2000 to 2026
$8.3M
VISION RESEARCHP30EY010608 · NEI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MASSEY, STEPHEN C · 1994 to 2014
$7.9M
NEI NIH HHS EY10608NEI NIH HHS EY12857NEI NIH HHS P30 EY010608NEI NIH HHS R01 EY012857
6 · The paper itself

Abstract

Gap junctions formed of connexin 36 (Cx36, also known as Gjd2) show tremendous functional plasticity on several time scales. Changes in connexin phosphorylation modify coupling in minutes through an order of magnitude, but recent studies also imply involvement of connexin turnover in regulating cell-cell communication. We utilized Cx36 with an internal HaloTag to study Cx36 turnover and trafficking in cultured cells. Irreversible, covalent pulse-chase labeling with fluorescent HaloTag ligands allowed clear discrimination of newly formed and pre-existing Cx36. Cx36 in junctional plaques turned over with a half-life of 3.1 h, and the turnover rate was unchanged by manipulations of protein kinase A (PKA) activity. In contrast, changes in PKA activity altered coupling within 20 min. New Cx36 in cargo vesicles was added directly to existing gap junctions and newly made Cx36 was not confined to points of addition, but diffused throughout existing gap junctions. Existing connexins also diffused into photobleached areas with a half-time of less than 2 s. In conclusion, studies of Cx36-HaloTag revealed novel features of connexin trafficking and demonstrated that phosphorylation-based changes in coupling occur on a different time scale than turnover.

Indexed as

AnimalsBrefeldin ACattleCell CommunicationCell LineConnexinsFluorescence Recovery After PhotobleachingGap Junction delta-2 ProteinGap JunctionsHeLa CellsHumansPhosphorylationBrefeldin AConnexinsGap Junction delta-2 ProteinConfocal microscopyConnexinGap junctionMembrane traffickingPulse-chaseTracer coupling

Identifiers

PMID26359298
PMCPMC4647165
OpenAlexW2217215314

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.