Evidence map›Paper›PMID 35017633›Full record

ArticleScientific reports2022

A new transgene mouse model using an extravesicular EGFP tag enables affinity isolation of cell-specific extracellular vesicles.

Mikkel Ø Nørgård, Lasse B Steffensen, Didde R Hansen, Ernst-Martin Füchtbauer, Morten B Engelund, Henrik Dimke, Ditte C Andersen, Per Svenningsen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

24 citing papers in PubMed, 27 citations in OpenAlex.

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  13. 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
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  18. Review
  19. Exomap1 mouse: A transgenic model forExtracellular vesicle · 2023
    Article
  20. Acute Kidney Injury by Ischemia/Reperfusion and Extracellular Vesicles.International journal of molecular sciences · 2023
    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 3 institutions in 1 country.

Mikkel Ø NørgårdDepartment of Molecular Medicine, Cardiovascular and Renal Research, University of Southern Denmark, J.B. Winsloews vej 21.3, 5000, Odense C, Denmark.
Lasse B SteffensenDepartment of Molecular Medicine, Cardiovascular and Renal Research, University of Southern Denmark, J.B. Winsloews vej 21.3, 5000, Odense C, Denmark.
Didde R HansenDepartment of Molecular Medicine, Cardiovascular and Renal Research, University of Southern Denmark, J.B. Winsloews vej 21.3, 5000, Odense C, Denmark.
Ernst-Martin FüchtbauerDepartment of Molecular Biology and Genetics, Aarhus University, Aarhus C, Denmark.
Morten B EngelundDepartment of Clinical Genetics, Odense University Hospital, Odense C, Denmark.
Henrik DimkeDepartment of Molecular Medicine, Cardiovascular and Renal Research, University of Southern Denmark, J.B. Winsloews vej 21.3, 5000, Odense C, Denmark.
Ditte C AndersenDCA-Lab, Department of Clinical Biochemistry and Pharmacology, Odense University Hospital, Odense C, Denmark.
Per SvenningsenDepartment of Molecular Medicine, Cardiovascular and Renal Research, University of Southern Denmark, J.B. Winsloews vej 21.3, 5000, Odense C, Denmark. psvenningsen@health.sdu.dk.
University of Southern Denmark · DKAarhus University · DKOdense University Hospital · DK

Funding

A.P. Møller og Hustru Chastine Mc-Kinney Møllers Fond til almene Formaal #20-L0112Carlsbergfondet #CF-180404Innovationsfonden #192200058BNovo Nordisk Fonden #NNF19OC0058222
6 · The paper itself

Abstract

The in vivo function of cell-derived extracellular vesicles (EVs) is challenging to establish since cell-specific EVs are difficult to isolate and differentiate. We, therefore, created an EV reporter using truncated CD9 to display enhanced green fluorescent protein (EGFP) on the EV surface. CD9truc-EGFP expression in cells did not affect EV size and concentration but enabled co-precipitation of EV markers TSG101 and ALIX from the cell-conditioned medium by anti-GFP immunoprecipitation. We then created a transgenic mouse where CD9truc-EGFP was inserted in the inverse orientation and double-floxed, ensuring irreversible Cre recombinase-dependent EV reporter expression. We crossed the EV reporter mice with mice expressing Cre ubiquitously (CMV-Cre), in cardiomyocytes (αMHC-MerCreMer) and renal tubular epithelial cells (Pax8-Cre), respectively. The CD9truc-EGFP positive mice showed Cre-dependent EGFP expression, and plasma CD9truc-EGFP EVs were immunoprecipitated only from CD9truc-EGFP positive CD9truc-EGFPxCMV-Cre and CD9truc-EGFPxαMHC-Cre mice, but not in CD9truc-EGFPxPax8-Cre and CD9truc-EGFP negative mice. In urine samples, CD9truc-EGFP EVs were detected by immunoprecipitation only in CD9truc-EGFP positive CD9truc-EGFPxCMV-Cre and CD9truc-EGFPxPax8-Cre mice, but not CD9truc-EGFPxαMHC-Cre and CD9truc-EGFP negative mice. In conclusion, our EV reporter mouse model enables Cre-dependent EV labeling, providing a new approach to studying cell-specific EVs in vivo and gaining a unique insight into their physiological and pathophysiological function.

Indexed as

AnimalsEpithelial CellsExtracellular VesiclesGenes, ReporterGreen Fluorescent ProteinsKidney Tubules, DistalMiceMice, TransgenicMyocytes, CardiacOrgan SpecificityTransgenesenhanced green fluorescent proteinGreen Fluorescent Proteins

Identifiers

PMID35017633
PMCPMC8752749
OpenAlexW4205106910

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.