Evidence map›Paper›PMID 9882629›Full record

ArticleThe Biochemical journal1999

Expression and subcellular localization of the ryanodine receptor in rat pancreatic acinar cells.

M F Leite, J A Dranoff, L Gao, M H Nathanson

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

26 citing papers in PubMed, 74 citations in OpenAlex.

  1. Modelling mechanism of calcium oscillations in pancreatic acinar cells.Journal of bioenergetics and biomembranes · 2014
    Article
  2. The ryanodine receptor is expressed in human pancreatic acinar cells and contributes to acinar cell injury.American journal of physiology. Gastrointestinal and liver physiology · 2014
    Article
  3. Article
  4. Article
  5. Calcium signaling in the liver.Comprehensive Physiology · 2013
    Review
  6. Ryanodine receptors contribute to bile acid-induced pathological calcium signaling and pancreatitis in mice.American journal of physiology. Gastrointestinal and liver physiology · 2012
    Article
  7. Article
  8. Article
  9. Dantrolene mitigates caerulein-induced pancreatitis in vivo in mice.American journal of physiology. Gastrointestinal and liver physiology · 2010
    Article
  10. Cyclic AMP accelerates calcium waves in pancreatic acinar cells.American journal of physiology. Gastrointestinal and liver physiology · 2008
    Article
  11. Effects of FK506 on ca release channels (review).Perspectives in medicinal chemistry · 2008
    Article
  12. Article
  13. Calcium signaling in cholangiocytes.World journal of gastroenterology · 2006
    Review
  14. The ryanodine receptor mediates early zymogen activation in pancreatitis.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
  15. Article
  16. Nuclear and cytosolic calcium are regulated independently.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
  17. Review
  18. Article
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

M F LeiteDepartment of Cell Biology, Yale University School of Medicine, New Haven, CT 06520, USA.
J A Dranoff
L Gao
M H Nathanson
Yale University · US

Funding

CALCIUM WAVES IN HEPATOCYTES--MECHANISMS AND EFFECTSR01DK045710 · NIDDK · YALE UNIVERSITY · PI NATHANSON, MICHAEL H · 1999 to 2014
$5.7M
BILE SECRETION AND INTRACELLULAR CA2+ SIGNALSR29DK045710 · NIDDK · YALE UNIVERSITY · PI NATHANSON, MICHAEL H · 1995 to 1999
–
NIDDK NIH HHS DK-45710
6 · The paper itself

Abstract

The ryanodine receptor (RyR) is the principal Ca2+-release channel in excitable cells, whereas the inositol 1,4,5-trisphosphate (InsP3) receptor (InsP3R) is primarily responsible for Ca2+ release in non-excitable cells, including epithelia. RyR also is expressed in a number of non-excitable cell types, but is thought to serve as an auxiliary or alternative Ca2+-release pathway in those cells. Here we use reverse transcription PCR to show that a polarized epithelium, the pancreatic acinar cell, expresses the type 2, but not the type 1 or 3, isoform of RyR. We furthermore use immunochemistry to demonstrate that the type 2 RyR is distributed throughout the basolateral and, to a lesser extent, the apical region of the acinar cell, but is excluded from the trigger zone, where cytosolic Ca2+ signals originate in this cell type. Since propagation of Ca2+ waves in acinar cells is sensitive to ryanodine, caffeine and Ca2+, these findings suggest that Ca2+ waves in this cell type result from the co-ordinated release of Ca2+, first from InsP3Rs in the trigger zone, then from RyRs elsewhere in the cell. RyR may play a fundamental role in Ca2+ signalling in polarized epithelia, including for Ca2+ signals initiated by InsP3.

Indexed as

AnimalsBase SequenceCell CompartmentationCloning, MolecularMicroscopy, ConfocalMolecular Sequence DataPancreasRatsReverse Transcriptase Polymerase Chain ReactionRyanodine Receptor Calcium Release ChannelSequence Analysis, DNARyanodine Receptor Calcium Release Channel

Identifiers

PMID9882629
PMCPMC1219966
OpenAlexW2043183187

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.