Evidence map›Paper›PMID 25809465›Full record

ArticleGene therapy2015

Optogenetic control of insulin secretion by pancreatic β-cells in vitro and in vivo.

T Kushibiki, S Okawa, T Hirasawa, M Ishihara

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Light-stimulated insulin secretion from pancreatic islet-like organoids derived from human pluripotent stem cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  5. Current Topics of Optogenetics for Medical Applications Toward Therapy.Advances in experimental medicine and biology · 2021
    Article
  6. Review
  7. Optogenetics: Therapeutic spark in neuropathic pain.Bosnian journal of basic medical sciences · 2019
    Review
  8. Light-Controlled Mammalian Cells and Their Therapeutic Applications in Synthetic Biology.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2019
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
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.

T KushibikiDepartment of Medical Engineering, National Defense Medical College, Tokorozawa, Saitama, Japan.
S OkawaDepartment of Medical Engineering, National Defense Medical College, Tokorozawa, Saitama, Japan.
T HirasawaDepartment of Medical Engineering, National Defense Medical College, Tokorozawa, Saitama, Japan.
M IshiharaDepartment of Medical Engineering, National Defense Medical College, Tokorozawa, Saitama, Japan.
National Defense Medical College · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study assessed the ability of optogenetics techniques to provide a better understanding of the control of insulin secretion, particularly regarding pancreatic β-cell function in homeostasis and pathological conditions such as diabetes mellitus (DM). We used optogenetics to investigate whether insulin secretion and blood glucose homeostasis could be controlled by regulating intracellular calcium ion concentrations ([Ca(2+)]i) in a mouse pancreatic β-cell line (MIN6) transfected with the optogenetic protein channelrhodopsin-2 (ChR2). The ChR2-transfected MIN6 (ChR2-MIN6) cells secreted insulin following irradiation with a laser (470 nm). The increase in [Ca(2+)]i was accompanied by elevated levels of messenger RNAs that encode calcium/calmodulin-dependent protein kinase II delta and adenylate cyclase 1. ChR2-MIN6 cells suspended in matrigel were inoculated into streptozotocin-induced diabetic mice that were then subjected to a glucose tolerance test. Laser irradiation of these mice caused a significant decrease in blood glucose, and the irradiated implanted cells expressed insulin. These findings demonstrate the power of optogenetics to precisely and efficiently controlled insulin secretion by pancreatic β-cells 'on demand', in contrast to techniques using growth factors or chemical inducers. Optogenetic technology shows great promise for understanding the mechanisms of glucose homeostasis and for developing treatments for metabolic diseases such as DM.

Indexed as

Low-Level Light TherapyOptogeneticsAdenylyl CyclasesAnimalsBlood GlucoseCalciumCalcium-Calmodulin-Dependent Protein Kinase Type 2Cells, CulturedChannelrhodopsinsDiabetes Mellitus, ExperimentalInsulinInsulin-Secreting CellsInsulin SecretionMiceStreptozocinadenylyl cyclase 1Adenylyl CyclasesBlood GlucoseCalciumCalcium-Calmodulin-Dependent Protein Kinase Type 2Camk2d protein, mouseChannelrhodopsinsInsulinStreptozocin

Identifiers

PMID25809465
OpenAlexW2062688282

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.