Evidence map›Paper›PMID 29975841›Full record

ArticleACS synthetic biology2018

Optical Activation of TrkA Signaling.

Liting Duan, Jen M Hope, Shunling Guo, Qunxiang Ong, Amaury François, Luke Kaplan, Grégory Scherrer, Bianxiao Cui

Open access · greenAbstract read
In one paragraph

Article in ACS synthetic biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
9.1field-weighted citation impact, top 3% 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

31 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Light-Inducible Deformation of Mitochondria in Live Cells.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  8. Article
  9. Article
  10. Review
  11. Optogenetic clustering and membrane translocation of the BcLOV4 photoreceptor.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. Neurite Outgrowth-Promoting Compounds from the Petals ofMolecules (Basel, Switzerland) · 2022
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

8 authors at 2 institutions in 1 country.

Liting DuanDepartment of Chemistry , Stanford University , Stanford , California 94305 , United States.
Jen M HopeDepartment of Chemistry , Stanford University , Stanford , California 94305 , United States.ORCID 0000-0002-9601-4778
Shunling GuoDepartment of Chemistry , Stanford University , Stanford , California 94305 , United States.
Qunxiang OngDepartment of Chemistry , Stanford University , Stanford , California 94305 , United States.
Amaury FrançoisDepartment of Anesthesiology, Perioperative and Pain Medicine, Department of Molecular and Cellular Physiology, Department of Neurosurgery , Stanford Neurosciences Institute, Stanford University , Palo Alto , California 94304 , United States.
Luke KaplanDepartment of Chemistry , Stanford University , Stanford , California 94305 , United States.
Grégory ScherrerDepartment of Anesthesiology, Perioperative and Pain Medicine, Department of Molecular and Cellular Physiology, Department of Neurosurgery , Stanford Neurosciences Institute, Stanford University , Palo Alto , California 94304 , United States.
Bianxiao CuiDepartment of Chemistry , Stanford University , Stanford , California 94305 , United States.ORCID 0000-0002-8044-5629
Stanford University · USNeurosciences Institute · US

Funding

Engineering external forces for manipulating cargo transport in live neuronsDP2NS082125 · NINDS · STANFORD UNIVERSITY · PI CUI, BIANXIAO · 2012 to 2012
$2.4M
NINDS NIH HHS DP2 NS082125
6 · The paper itself

Abstract

Nerve growth factor/tropomyosin receptor kinase A (NGF/TrkA) signaling plays a key role in neuronal development, function, survival, and growth. The pathway is implicated in neurodegenerative disorders including Alzheimer's disease, chronic pain, inflammation, and cancer. NGF binds the extracellular domain of TrkA, leading to the activation of the receptor's intracellular kinase domain. As TrkA signaling is highly dynamic, mechanistic studies would benefit from a tool with high spatial and temporal resolution. Here we present the design and evaluation of four strategies for light-inducible activation of TrkA in the absence of NGF. Our strategies involve the light-sensitive protein Arabidopsis cryptochrome 2 and its binding partner CIB1. We demonstrate successful recapitulation of native NGF/TrkA functions by optical induction of plasma membrane recruitment and homo-interaction of the intracellular domain of TrkA. This approach activates PI3K/AKT and Raf/ERK signaling pathways, promotes neurite growth in PC12 cells, and supports survival of dorsal root ganglion neurons in the absence of NGF. This ability to activate TrkA using light bestows high spatial and temporal resolution for investigating NGF/TrkA signaling.

Indexed as

AnimalsCell MembraneCell SurvivalGanglia, SpinalNerve Growth FactorPC12 CellsPhosphatidylinositol 3-KinasesPhosphorylationRatsReceptor, trkASignal TransductionNerve Growth FactorPhosphatidylinositol 3-KinasesReceptor, trkA

Identifiers

PMID29975841
PMCPMC7361323
OpenAlexW2793545699

What OpenQuestion holds

Textmetadata
LicenceTDM
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.