Evidence map›Paper›PMID 23479634›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

Optically triggering spatiotemporally confined GPCR activity in a cell and programming neurite initiation and extension.

W K Ajith Karunarathne, Lopamudra Giri, Vani Kalyanaraman, N Gautam

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

49 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
  2. Optogenetic engineering for ion channel modulation.Current opinion in chemical biology · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Selective optogenetic control of GNature communications · 2022
    Article
  13. Optogenetics for light control of biological systems.Nature reviews. Methods primers · 2022
    Article
  14. Article
  15. Review
  16. Live Cell Imaging and Optogenetics-Based Assays for GPCR Activity.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  17. Optogenetic Stimulation of GFrontiers in physiology · 2021
    Article
  18. Review
  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.

W K Ajith KarunarathneDepartment of Anesthesiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Lopamudra Giri
Vani Kalyanaraman
N Gautam
Washington University in St. Louis · US

Funding

SIGNALING IN LIVING CELLSR01GM069027 · NIGMS · WASHINGTON UNIVERSITY · PI GAUTAM, NARASIMHAN · 2004 to 2016
$3.2M
G PROTEIN SUBUNIT FUNCTIONR01GM080558 · NIGMS · WASHINGTON UNIVERSITY · PI GAUTAM, NARASIMHAN · 2008 to 2011
$1.8M
NIGMS NIH HHS GM069027NIGMS NIH HHS GM080558NIGMS NIH HHS R01 GM069027NIGMS NIH HHS R01 GM080558
6 · The paper itself

Abstract

G-protein-coupled receptor (GPCR) activity gradients evoke important cell behavior but there is a dearth of methods to induce such asymmetric signaling in a cell. Here we achieved reversible, rapidly switchable patterns of spatiotemporally restricted GPCR activity in a single cell. We recruited properties of nonrhodopsin opsins--rapid deactivation, distinct spectral tuning, and resistance to bleaching--to activate native Gi, Gq, or Gs signaling in selected regions of a cell. Optical inputs were designed to spatiotemporally control levels of second messengers, IP3, phosphatidylinositol (3,4,5)-triphosphate, and cAMP in a cell. Spectrally selective imaging was accomplished to simultaneously monitor optically evoked molecular and cellular response dynamics. We show that localized optical activation of an opsin-based trigger can induce neurite initiation, phosphatidylinositol (3,4,5)-triphosphate increase, and actin remodeling. Serial optical inputs to neurite tips can refashion early neuron differentiation. Methods here can be widely applied to program GPCR-mediated cell behaviors.

Indexed as

LightCyclic AMPFluorescence Resonance Energy TransferHumansNeuritesOpsinsPhosphatidylinositol PhosphatesReceptors, G-Protein-CoupledSignal TransductionTime-Lapse ImagingCyclic AMPOpsinsphosphatidylinositol 3,4,5-triphosphatePhosphatidylinositol PhosphatesReceptors, G-Protein-Coupled

Identifiers

PMID23479634
PMCPMC3637763
OpenAlexW1983111827

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.