Evidence map›Paper›PMID 27893730›Full record

ArticleNature nanotechnology2017

Fluorescent nanodiamond tracking reveals intraneuronal transport abnormalities induced by brain-disease-related genetic risk factors.

Simon Haziza, Nitin Mohan, Yann Loe-Mie, Aude-Marie Lepagnol-Bestel, Sophie Massou, Marie-Pierre Adam, Xuan Loc Le, Julia Viard, Christine Plancon, Rachel Daudin and 13 more

Abstract readLetter
PubMed Publisher
In one paragraph

Article in Nature nanotechnology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
5.6field-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

39 citing papers in PubMed, 137 citations in OpenAlex.

  1. Article
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  10. Review
  11. Review
  12. On-Demand, Direct Printing of Nanodiamonds at the Quantum Level.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
    Article
  13. Review
  14. Review
  15. Review
  16. Time for NanoNeuro.Nature methods · 2021
    Review
  17. Article
  18. Dual-process brain mitochondria isolation preserves function and clarifies protein composition.Proceedings of the National Academy of Sciences of the United States of America · 2021
    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

23 authors at 8 institutions in 4 countries.

Simon HazizaLaboratoire Aimé Cotton, CNRS, Université Paris-Sud, ENS Cachan, Université Paris-Saclay, 91405 Orsay, France.
Nitin MohanLaboratoire Aimé Cotton, CNRS, Université Paris-Sud, ENS Cachan, Université Paris-Saclay, 91405 Orsay, France.
Yann Loe-MieCentre de Psychiatrie et Neurosciences, INSERM U894, Université Paris-Descartes, 75014 Paris, France.
Aude-Marie Lepagnol-BestelCentre de Psychiatrie et Neurosciences, INSERM U894, Université Paris-Descartes, 75014 Paris, France.
Sophie MassouLaboratoire Aimé Cotton, CNRS, Université Paris-Sud, ENS Cachan, Université Paris-Saclay, 91405 Orsay, France.
Marie-Pierre AdamLaboratoire Aimé Cotton, CNRS, Université Paris-Sud, ENS Cachan, Université Paris-Saclay, 91405 Orsay, France.
Xuan Loc LeLaboratoire Aimé Cotton, CNRS, Université Paris-Sud, ENS Cachan, Université Paris-Saclay, 91405 Orsay, France.
Julia ViardCentre de Psychiatrie et Neurosciences, INSERM U894, Université Paris-Descartes, 75014 Paris, France.
Christine PlanconCommissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Institut de Génomique, Centre National de Génotypage, 91057 Evry, France.
Rachel DaudinCentre de Psychiatrie et Neurosciences, INSERM U894, Université Paris-Descartes, 75014 Paris, France.
Pascale KoebelInstitut de génétique et de biologie moléculaire et cellulaire, CNRS UMR 7104, INSERM U 964, Université de Strasbourg, 67400 Illkirch-Graffenstaden, France.
Emilie DorardCentre de Psychiatrie et Neurosciences, INSERM U894, Université Paris-Descartes, 75014 Paris, France.
Christiane RoseCentre de Psychiatrie et Neurosciences, INSERM U894, Université Paris-Descartes, 75014 Paris, France.
Feng-Jen HsiehInstitute of Atomic and Molecular Sciences, Academia Sinica, Taipei 106, Taiwan.
Chih-Che WuDepartment of Applied Chemistry, National Chi Nan University, Puli, Nantou Hsien 545, Taiwan.
Brigitte PotierCentre de Psychiatrie et Neurosciences, INSERM U894, Université Paris-Descartes, 75014 Paris, France.
Yann HeraultInstitut de génétique et de biologie moléculaire et cellulaire, CNRS UMR 7104, INSERM U 964, Université de Strasbourg, 67400 Illkirch-Graffenstaden, France.
Carlo SalaNeuroscience Institute, CNR, 20129 Milano, Italy.
Aiden CorvinDepartment of Psychiatry, Institute of Neuroscience, Trinity College Dublin, Dublin 2, Ireland.
Bernadette AllinquantCentre de Psychiatrie et Neurosciences, INSERM U894, Université Paris-Descartes, 75014 Paris, France.
Huan-Cheng ChangInstitute of Atomic and Molecular Sciences, Academia Sinica, Taipei 106, Taiwan.
François TreussartLaboratoire Aimé Cotton, CNRS, Université Paris-Sud, ENS Cachan, Université Paris-Saclay, 91405 Orsay, France.ORCID 0000-0002-1755-0688
Michel SimonneauLaboratoire Aimé Cotton, CNRS, Université Paris-Sud, ENS Cachan, Université Paris-Saclay, 91405 Orsay, France.
Délégation Paris 5 · FRUniversité Paris-Sud · FRCentre National de la Recherche Scientifique · FRInstitute of Atomic and Molecular Sciences, Academia Sinica · TWCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRNational Chi Nan University · TWNeuroscience Institute · ITTrinity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain diseases such as autism and Alzheimer's disease (each inflicting >1% of the world population) involve a large network of genes displaying subtle changes in their expression. Abnormalities in intraneuronal transport have been linked to genetic risk factors found in patients, suggesting the relevance of measuring this key biological process. However, current techniques are not sensitive enough to detect minor abnormalities. Here we report a sensitive method to measure the changes in intraneuronal transport induced by brain-disease-related genetic risk factors using fluorescent nanodiamonds (FNDs). We show that the high brightness, photostability and absence of cytotoxicity allow FNDs to be tracked inside the branches of dissociated neurons with a spatial resolution of 12 nm and a temporal resolution of 50 ms. As proof of principle, we applied the FND tracking assay on two transgenic mouse lines that mimic the slight changes in protein concentration (∼30%) found in the brains of patients. In both cases, we show that the FND assay is sufficiently sensitive to detect these changes.

Indexed as

Alzheimer DiseaseAutistic DisorderHippocampusNeuronsAnimalsBiological Transport, ActiveCells, CulturedCell TrackingMiceMice, TransgenicMicroscopy, FluorescenceMicroscopy, VideoNanodiamondsNanodiamonds

Identifiers

PMID27893730
OpenAlexW2549132203

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.