Evidence map›Paper›PMID 30356209›Full record

ReviewNature reviews. Endocrinology2018

Optical tools for understanding the complexity of β-cell signalling and insulin release.

James A Frank, Johannes Broichhagen, Dmytro A Yushchenko, Dirk Trauner, Carsten Schultz, David J Hodson

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Endocrinology, 2018. 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. Review
  3. Fine-tuned photochromic sulfonylureas for optical control of beta cell CaDiabetic medicine : a journal of the British Diabetic Association · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. PDX1Nature communications · 2021
    Article
  15. Review
  16. Article
  17. Functional analysis of islet cells in vitro, in situ, and in vivo.Seminars in cell & developmental biology · 2020
    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

6 authors.

James A FrankResearch Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, MA, USA.
Johannes BroichhagenDepartment of Chemical Biology, Max Planck Institute for Medical Research, Heidelberg, Germany.ORCID http://orcid.org/0000-0003-3084-6595
Dmytro A YushchenkoInstitute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Prague, Czech Republic.
Dirk TraunerResearch Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-6782-6056
Carsten SchultzEuropean Molecular Biology Laboratory (EMBL), Cell Biology and Biophysics Unit, Heidelberg, Germany. schulcar@ohsu.edu.
David J HodsonInstitute of Metabolism and Systems Research (IMSR) and Centre of Membrane Proteins and Receptors (COMPARE), University of Birmingham, Birmingham, UK. d.hodson@bham.ac.uk.ORCID http://orcid.org/0000-0002-8641-8568

Funding

Medical Research Council MR/N00275X/1
6 · The paper itself

Abstract

Following stimulation, pancreatic β-cells must orchestrate a plethora of signalling events to ensure the appropriate release of insulin and maintenance of normal glucose homeostasis. Failure at any point in this cascade leads to impaired insulin secretion, elevated blood levels of glucose and eventually type 2 diabetes mellitus. Likewise, β-cell replacement or regeneration strategies for the treatment of both type 1 and type 2 diabetes mellitus might fail if the correct cell signalling phenotype cannot be faithfully recreated. However, current understanding of β-cell function is complicated because of the highly dynamic nature of their intracellular and intercellular signalling as well as insulin release itself. β-Cells must precisely integrate multiple signals stemming from multiple cues, often with differing intensities, frequencies and cellular and subcellular localizations, before converging these signals onto insulin exocytosis. In this respect, optical approaches with high resolution in space and time are extremely useful for properly deciphering the complexity of β-cell signalling. An increased understanding of β-cell signalling might identify new mechanisms underlying insulin release, with relevance for future drug therapy and de novo stem cell engineering of functional islets.

Indexed as

AnimalsDiabetes Mellitus, Type 2Genetic Predisposition to DiseaseGlucoseHomeostasisHumansIncidenceInsulin-Secreting CellsInsulin SecretionRisk AssessmentSensitivity and SpecificitySignal TransductionGlucose

Identifiers

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.