Evidence map›Paper›PMID 8022804›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1994

Switch in gap junction protein expression is associated with selective changes in junctional permeability during keratinocyte differentiation.

J L Brissette, N M Kumar, N B Gilula, J E Hall, G P Dotto

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

35 citing papers in PubMed, 140 citations in OpenAlex.

  1. Article
  2. Article
  3. Contribution of Keratinocytes in Skin Cancer Initiation and Progression.International journal of molecular sciences · 2024
    Review
  4. Article
  5. Article
  6. Review
  7. The Role of GJD2(Cx36) in Refractive Error Development.Investigative ophthalmology & visual science · 2022
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Gap junctions in inherited human disease.Pflugers Archiv : European journal of physiology · 2010
    Review
  18. Review
  19. 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

5 authors at 2 institutions in 1 country.

J L BrissetteDepartment of Dermatology, Harvard Medical School, Charlestown, MA 02129.
N M Kumar
N B Gilula
J E Hall
G P Dotto
Scripps Research Institute · USUniversity of California, Irvine · US

Funding

GROWTH DIFFERENTIATION CONTROL IN PRIMARY KERATINOCYTES.R01AR039190 · NIAMS · YALE UNIVERSITY · PI DOTTO, GIAN-PAOLO · 1988 to 2021
$9.5M
GAP JUNCTIONS AND CELL-CELL COMMUNICATIONR37GM037904 · NIGMS · SCRIPPS RESEARCH INSTITUTE · PI GILULA, NORTON B · 1991 to 2000
$536k
GAP JUNCTION AND CELL-CELL COMMUNICATIONR01GM037904 · NIGMS · SCRIPPS RESEARCH INSTITUTE · PI GILULA, NORTON B · 1986 to 1989
–
NCI NIH HHS CA 16083NIAMS NIH HHS AR 39190NIGMS NIH HHS GM 37904
6 · The paper itself

Abstract

Gap junctional communication provides a mechanism for regulating multicellular activities by allowing the exchange of small diffusible molecules between neighboring cells. The diversity of gap junction proteins may exist to form channels that have different permeability properties. We report here that induction of terminal differentiation in mouse primary keratinocytes by calcium results in a specific switch in gap junction protein expression. Expression of alpha 1 (connexin 43) and beta 2 (connexin 26) gap junction proteins is down-modulated, whereas that of beta 3 (connexin 31) and beta 4 (connexin 31.1) proteins is induced. Although both proliferating and differentiating keratinocytes are electrically coupled, there are significant changes in the permeability properties of the junctions to small molecules. In parallel with the changes in gap junction protein expression during differentiation, the intercellular transfer of the small dyes neurobiotin, carboxyfluorescein, and Lucifer yellow is significantly reduced, whereas that of small metabolites, such as nucleotides and amino acids, proceeds unimpeded. Thus, a switch in gap junction protein expression in differentiating keratinocytes is accompanied by selective changes in junctional permeability that may play an important role in the coordinate control of the differentiation process.

Indexed as

AnimalsAnimals, NewbornBiotinCalciumCell DifferentiationCells, CulturedConnexinsElectric ConductivityElectrophysiologyFluoresceinsFluorescent DyesImmunoblottingIntercellular JunctionsIsoquinolinesKeratinocytesMice6-carboxyfluoresceinBiotinCalciumConnexinsFluoresceinsFluorescent DyesIsoquinolineslucifer yellowneurobiotin

Identifiers

PMID8022804
PMCPMC44220
OpenAlexW2040247477

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.