Evidence map›Paper›PMID 12960432›Full record

ArticleMolecular biology of the cell2003

Polarization of specific tropomyosin isoforms in gastrointestinal epithelial cells and their impact on CFTR at the apical surface.

Jacqueline Rae Dalby-Payne, Edward Vincent O'Loughlin, Peter Gunning

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Actin-tropomyosin distribution in non-muscle cells.Journal of muscle research and cell motility · 2020
    Review
  4. Article
  5. Article
  6. Article
  7. Tropomyosin is required for cardiac morphogenesis, myofibril assembly, and formation of adherens junctions in the developing mouse embryo.Developmental dynamics : an official publication of the American Association of Anatomists · 2014
    Article
  8. Review
  9. Tropomyosin isoforms and reagents.Bioarchitecture · 2011
    Article
  10. Article
  11. Article
  12. New insights into the regulation of the actin cytoskeleton by tropomyosin.International review of cell and molecular biology · 2010
    Review
  13. Article
  14. Diverse roles of the actin cytoskeleton in striated muscle.Journal of muscle research and cell motility · 2009
    Review
  15. Article
  16. Article
  17. Article
  18. 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

3 authors at 1 institution in 1 country.

Jacqueline Rae Dalby-PayneGastroenterology Research, The Children's Hospital at Westmead, Westmead, NSW Z145, Australia.
Edward Vincent O'Loughlin
Peter Gunning
The University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microfilaments have been reported to be polarized in a number of cell types based both on function and isoform composition. There is evidence that microfilaments are involved in the movement of vesicles and the polarized delivery of proteins to specialized membrane domains. We have investigated the composition of actin microfilaments in gastrointestinal epithelial cells and their role in the delivery of the cystic fibrosis transmembrane conductance regulator (CFTR) into the apical membrane using cultured T84 cells as a model. We identified a specific population of microfilaments containing the tropomyosin (Tm) isoforms Tm5a and/or Tm5b, which are polarized in T84 cell monolayers. Polarization of this microfilament population occurs very rapidly in response to cell-cell and cell-substratum contact and is not inhibited by jasplakinolide, suggesting this involves the movement of intact filaments. Colocalization of Tm5a and/or Tm5b and CFTR was observed in long-term cultures. A reduction in Tm5a and Tm5b expression, induced using antisense oligonucleotides, resulted in an increase in both CFTR surface expression and chloride efflux in response to cAMP stimulation. We conclude that Tm isoforms Tm5a and/or Tm5b mark an apical population of microfilaments that can regulate the insertion and/or retention of CFTR into the plasma membrane.

Indexed as

DepsipeptidesActin CytoskeletonActinsAntineoplastic AgentsCell AdhesionChloridesCyclic AMPCystic Fibrosis Transmembrane Conductance RegulatorEpithelial CellsGastrointestinal TractHumansOligonucleotides, AntisensePeptides, CyclicProtein IsoformsProtein TransportTropomyosinActinsAntineoplastic AgentsCFTR protein, humanChloridesCyclic AMPCystic Fibrosis Transmembrane Conductance RegulatorDepsipeptidesjasplakinolideOligonucleotides, AntisensePeptides, CyclicProtein IsoformsTPM3 protein, humanTropomyosin

Identifiers

PMID12960432
PMCPMC266757
OpenAlexW2145744808

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.