Evidence map›Paper›PMID 30816224›Full record

ArticleScientific reports2019

A transgenic inducible GFP extracellular-vesicle reporter (TIGER) mouse illuminates neonatal cortical astrocytes as a source of immunomodulatory extracellular vesicles.

Victoria N Neckles, Mary C Morton, Jennie C Holmberg, Aidan M Sokolov, Timothy Nottoli, Don Liu, David M Feliciano

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

43 citing papers in PubMed, 59 citations in OpenAlex.

  1. A Novel Reporter Mouse for Astrocyte-Derived Extracellular Vesicles Reveals Enrichment of Cargo at Neuronal Mitochondria.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  9. Exosome: an overview on enhanced biogenesis by small molecules.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
  10. Article
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  12. Isolation and characterization of bone mesenchymal cell small extracellular vesicles using a novel mouse model.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Article
  13. Extracellular Vesicle-Mediated Neuron-Glia Communications in the Central Nervous System.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Review
  14. Proteomic analysis and in vivo visualization of extracellular vesicles from mouse oviducts during pre-implantation embryo development.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
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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

7 authors at 2 institutions in 1 country.

Victoria N NecklesDepartment of Biological Sciences, Clemson University, Clemson, SC, 29634-0314, USA.
Mary C MortonDepartment of Biological Sciences, Clemson University, Clemson, SC, 29634-0314, USA.
Jennie C HolmbergDepartment of Biological Sciences, Clemson University, Clemson, SC, 29634-0314, USA.
Aidan M SokolovDepartment of Biological Sciences, Clemson University, Clemson, SC, 29634-0314, USA.
Timothy NottoliYale Genome Editing Center, Department of Comparative Medicine, Yale School of Medicine, PO Box 208016, New Haven, CT, 06520-8016, USA.
Don LiuCharles River Laboratories, 261 Ballardvale Street, Wilmington, MA, 01887, USA.
David M FelicianoDepartment of Biological Sciences, Clemson University, Clemson, SC, 29634-0314, USA. dfelici@clemson.edu.
Clemson University · USCharles River Laboratories (United States) · US

Funding

SLC7A5-MTOR Regulation of Neural DevelopmentR15NS096562 · NINDS · CLEMSON UNIVERSITY · PI FELICIANO, DAVID MATTHEW · 2016 to 2016
$442k
NINDS NIH HHS R15 NS096562
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are cellular derived particles found throughout the body in nearly all tissues and bodily fluids. EVs contain biological molecules including small RNAs and protein. EVs are proposed to be transferred between cells, notably, cells of the immune system. Tools that allow for in vivo EV labeling while retaining the ability to resolve cellular sources and timing of release are required for a full understanding of EV functions. Fluorescent EV fusion proteins are useful for the study of EV biogenesis, release, and identification of EV cellular recipients. Among the most plentiful and frequently identified EV proteins is CD9, a tetraspanin protein. A transgenic mouse containing a CRE-recombinase inducible CAG promoter driven CD9 protein fused to Turbo-GFP derived from the copepod Pontellina plumata was generated as an EV reporter. The transgenic inducible GFP EV reporter (TIGER) mouse was electroporated with CAG-CRE plasmids or crossed with tamoxifen inducible CAG-CRE-ER

Indexed as

AnimalsAstrocytesBiomarkersCells, CulturedExtracellular VesiclesGreen Fluorescent ProteinsLateral VentriclesMiceMice, TransgenicMicrogliaMicroRNAsRecombinant Fusion ProteinsTetraspanin 29BiomarkersCd9 protein, mouseGreen Fluorescent ProteinsMicroRNAsRecombinant Fusion ProteinsTetraspanin 29

Identifiers

PMID30816224
PMCPMC6395689
OpenAlexW2915804742

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.