Evidence map›Paper›PMID 15630435›Full record

ArticleThe Journal of clinical investigation2005

CaV2.3 channel and PKClambda: new players in insulin secretion.

Shao-Nian Yang, Per-Olof Berggren

Abstract readComment
In one paragraph

Article in The Journal of clinical investigation, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Article
  2. Association Study ofInternational journal of molecular sciences · 2024
    Article
  3. Review
  4. Review
  5. In Vivo CaBiomedicines · 2023
    Article
  6. Article
  7. Review
  8. Breeding of CaScientific reports · 2021
    Article
  9. Enhanced expression of β cell CaProceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  10. Review
  11. Review
  12. Review
  13. Loss of αDiabetes · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Ionic mechanisms in pancreatic β cell signaling.Cellular and molecular life sciences : CMLS · 2014
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Shao-Nian YangThe Rolf Luft Center for Diabetes Research, Karolinska Diabetes Center, Department of Molecular Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Per-Olof Berggren

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insulin secretion is critically dependent on the proper function of a complex molecular network. Ca(V)2.3-knockout (Ca(V)2.3(-/-)) and PKClambda-knockout (PKClambda(-/-)) mouse models now suggest that these 2 players, the Ca(v)2.3 channel and PKClambda, are important constituents of this molecular network. Subsequent to glucose stimulation, insulin is released from the pancreatic beta cell in a biphasic pattern, i.e., a rapid initial phase followed by a slower, more sustained phase. Interestingly, Ca(2+) influx through the Ca(V)2.3 channel regulates only the second phase of insulin secretion. PKClambda seems to enter the beta cell nucleus and in turn modulates the expression of several genes critical for beta cell secretory function. Studies by Hashimoto et al. and Jing et al. in this issue of the JCI set out to answer the question of why numerous isoforms of proteins with similar functions are present in the beta cell. This is important, since it has been difficult to understand the modulatory and/or regulatory roles of different isoforms of proteins in defined subcellular compartments and at various times during the secretory process in both beta cell physiology and pathophysiology.

Indexed as

AnimalsCalciumCalcium ChannelsCalcium Channels, R-TypeCation Transport ProteinsGene Expression RegulationHumansInsulinInsulin SecretionIslets of LangerhansIsoenzymesProtein IsoformsProtein Kinase CProtein Kinase C-lambdaCACNA1E protein, humanCalciumCalcium ChannelsCalcium Channels, R-TypeCation Transport ProteinsInsulinIsoenzymesProtein IsoformsProtein Kinase CProtein Kinase C-lambda

Identifiers

PMID15630435
PMCPMC539207

What Socratic 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 Socratic graph.