Evidence map›Paper›PMID 24349395›Full record

ArticlePloS one2013

In vivo characterization of dynein-driven nanovectors using Drosophila oocytes.

Nadège Parassol, Céline Bienvenu, Cécile Boglio, Sébastien Fiorucci, Delphine Cerezo, Xiao-Min Yu, Guilhem Godeau, Jacques Greiner, Pierre Vierling, Stéphane Noselli and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 92% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

12 authors at 5 institutions in 1 country.

Nadège ParassolUniversity of Nice Sophia-Antipolis, Institute of Biology Valrose (iBV), UMR 7277-CNRS, UMR 1091 INSERM, Nice, France.
Céline BienvenuUniversité de Nice Sophia-Antipolis, Institut de Chimie de Nice (ICN), UMR 7272-CNRS, Nice, France.
Cécile BoglioUniversité de Nice Sophia-Antipolis, Institut de Chimie de Nice (ICN), UMR 7272-CNRS, Nice, France.
Sébastien FiorucciUniversité de Nice Sophia-Antipolis, Institut de Chimie de Nice (ICN), UMR 7272-CNRS, Nice, France.
Delphine CerezoUniversity of Nice Sophia-Antipolis, Institute of Biology Valrose (iBV), UMR 7277-CNRS, UMR 1091 INSERM, Nice, France.
Xiao-Min YuUniversité de Nice Sophia-Antipolis, Institut de Chimie de Nice (ICN), UMR 7272-CNRS, Nice, France.
Guilhem GodeauUniversité de Nice Sophia-Antipolis, Institut de Chimie de Nice (ICN), UMR 7272-CNRS, Nice, France.
Jacques GreinerUniversité de Nice Sophia-Antipolis, Institut de Chimie de Nice (ICN), UMR 7272-CNRS, Nice, France.
Pierre VierlingUniversité de Nice Sophia-Antipolis, Institut de Chimie de Nice (ICN), UMR 7272-CNRS, Nice, France.
Stéphane NoselliUniversity of Nice Sophia-Antipolis, Institute of Biology Valrose (iBV), UMR 7277-CNRS, UMR 1091 INSERM, Nice, France.
Christophe Di GiorgioUniversité de Nice Sophia-Antipolis, Institut de Chimie de Nice (ICN), UMR 7272-CNRS, Nice, France.
Véronique Van De BorUniversity of Nice Sophia-Antipolis, Institute of Biology Valrose (iBV), UMR 7277-CNRS, UMR 1091 INSERM, Nice, France.
Centre National de la Recherche Scientifique · FRUniversité Côte d'Azur · FRInserm · FRInstitut de Biologie Valrose · FRInstitut de Chimie de Nice · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular motors transport various cargoes including vesicles, proteins and mRNAs, to distinct intracellular compartments. A significant challenge in the field of nanotechnology is to improve drug nuclear delivery by engineering nanocarriers transported by cytoskeletal motors. However, suitable in vivo models to assay transport and delivery efficiency remain very limited. Here, we develop a fast and genetically tractable assay to test the efficiency and dynamics of fluospheres (FS) using microinjection into Drosophila oocytes coupled with time-lapse microscopy. We designed dynein motor driven FS using a collection of dynein light chain 8 (LC8) peptide binding motifs as molecular linkers and characterized in real time the efficiency of the FS movement according to its linker's sequence. Results show that the conserved LC8 binding motif allows fast perinuclear nanoparticle's accumulation in a microtubule and dynein dependent mechanism. These data reveal the Drosophila oocyte as a new valuable tool for the design of motor driven nanovectors.

Indexed as

Drug Delivery SystemsAnimalsBiological Transport, ActiveCytoskeletonDrosophila melanogasterDrosophila ProteinsDyneinsNanoparticlesOocytesDrosophila ProteinsDyneins

Identifiers

PMID24349395
PMCPMC3861458
OpenAlexW2024922005

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.