Evidence map›Paper›PMID 7529626›Full record

ArticleIn vitro cellular & developmental biology. Animal1994

Mouse pancreatic acinar/ductular tissue gives rise to epithelial cultures that are morphologically, biochemically, and functionally indistinguishable from interlobular duct cell cultures.

S Githens, J A Schexnayder, R L Moses, G M Denning, J J Smith, M L Frazier

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 1994. 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
1.7field-weighted citation impact, top 16% 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, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Development of a polarized pancreatic ductular cell epithelium for physiological studies.Journal of applied physiology (Bethesda, Md. : 1985) · 2018
    Article
  5. Article
  6. Review
  7. Article
  8. c-Jun/AP-1 is required for CCK-induced pancreatic acinar cell dedifferentiation and DNA synthesis in vitro.American journal of physiology. Gastrointestinal and liver physiology · 2012
    Article
  9. Review
  10. Review
  11. Conservation of the TGFbeta/Labial homeobox signaling loop in endoderm-derived cells between Drosophila and mammals.Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] · 2010
    Article
  12. Article
  13. Article
  14. Article
  15. In vitro cultivation of human islets from expanded ductal tissue.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
  16. Article
  17. A mouse model for the delta F508 allele of cystic fibrosis.The Journal of clinical investigation · 1995
    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

6 authors at 4 institutions in 1 country.

S GithensDepartment of Biological Sciences, University of New Orleans, LA 70148.
J A Schexnayder
R L Moses
G M Denning
J J Smith
M L Frazier
University of Iowa · USAnderson Hospital · USUniversity Medical Center New Orleans · USUniversity of New Orleans · US

Funding

TRANSGENIC ANM MODEL/PANCREATIC DUCT CELL ADENOCARCINOMAR01CA049667 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI FRAZIER, MARSHA L. · 1989 to 1991
–
NCI NIH HHS R01-CA49667
6 · The paper itself

Abstract

Most of the pancreatic exocrine epithelium consists of acinar and intralobular duct (ductular) cells, with the balance consisting of interlobular and main duct cells. Fragments of mouse acinar/ductular epithelium can be isolated by partial digestion with collagenase and purified by Ficoll density gradient centrifugation. We investigated whether previously developed culture conditions used for duct epithelium would result in the selective survival and proliferation of ductular cells from the acinar/ductular fragments. The fragments were cultured on nitrocellulose filters coated with extracellular matrix. After 2 to 4 wk the filters were covered with proliferating cells resembling parallel cultures of duct epithelium by the following criteria: protein/DNA ratio, light and electron microscopic appearance, the presence of duct markers (carbonic anhydrase [CA] activity, CA II mRNA, the cystic fibrosis transmembrane conductance regulator), the near absence of acinar cell markers (amylase and chymotrypsin), a similar polypeptide profile after sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and the presence of spontaneous and secretin-stimulated electrogenic ion transport. Both duct and ductular epithelia formed fluid-filled cysts in collagen gels and both could be subcultured. We conclude that acinar/ductular tissue gives rise to ductular cells in culture by some combination of acinar cell death and/or transdifferentiation to a ductular phenotype, accompanied by proliferation of these cells and preexisting ductular cells. These cultures may be used to investigate the properties of this part of the pancreatic duct system, from which most of the pancreatic juice water and electrolytes probably originates.

Indexed as

AmylasesAnimalsCarbonic AnhydrasesCell DivisionCells, CulturedCell SurvivalChymotrypsinCulture MediaDNAElectric ConductivityEpithelial CellsMaleMiceMicroscopy, ElectronMicroscopy, Electron, ScanningPancreasAmylasesCarbonic AnhydrasesChymotrypsinCulture MediaDNAProteins

Identifiers

PMID7529626
OpenAlexW2020687437

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.