Evidence map›Paper›PMID 33898459›Full record

ArticleFrontiers in cell and developmental biology2021

Visualization and Identification of Bioorthogonally Labeled Exosome Proteins Following Systemic Administration in Mice.

Eric Zhang, Yanwen Liu, Chaoshan Han, Chengming Fan, Lu Wang, Wangping Chen, Yipeng Du, Dunzheng Han, Baron Arnone, Shiyue Xu and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

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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

13 authors at 1 institution in 1 country.

Eric ZhangDepartment of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
Yanwen LiuDepartment of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
Chaoshan HanDepartment of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
Chengming FanDepartment of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
Lu WangDepartment of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
Wangping ChenDepartment of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
Yipeng DuDepartment of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
Dunzheng HanDepartment of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
Baron ArnoneDepartment of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
Shiyue XuDepartment of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
Yuhua WeiDepartment of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
James MobleyDepartment of Anesthesiology and Perioperative Medicine, University of Alabama at Birmingham, School of Medicine, Birmingham, AL, United States.
Gangjian QinDepartment of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, AL, United States.
University of Alabama at Birmingham · US

Funding

E2F2 and Vascular FunctionR01HL138990 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI NAKADA, YUJI · 2017 to 2020
$2.3M
CXCR4 and ckit signaling in BM progenitor cell recruitment in the ischemic heartR01HL113541 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI QIN, GANGJIAN · 2012 to 2015
$1.5M
GOLPH3 in vascular smooth muscle cell biology and vascular diseaseR01HL130052 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI QIN, GANGJIAN · 2016 to 2019
$1.5M
E2F1 in BM progenitor cell differentiation and cardiovascular repairR01HL131110 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI QIN, GANGJIAN, ZHAO, MING · 2016 to 2019
$1.5M
NHLBI NIH HHS R01 HL113541NHLBI NIH HHS R01 HL130052NHLBI NIH HHS R01 HL131110NHLBI NIH HHS R01 HL138990
6 · The paper itself

Abstract

Exosomes transport biologically active cargo (e.g., proteins and microRNA) between cells, including many of the paracrine factors that mediate the beneficial effects associated with stem-cell therapy. Stem cell derived exosomes, in particular mesenchymal stem cells (MSCs), have been shown previously to largely replicate the therapeutic activity associated with the cells themselves, which suggests that exosomes may be a useful cell-free alternative for the treatment of cardiovascular disorders. However, the mechanisms that govern how exosomes home to damaged cells and tissues or the uptake and distribution of exosomal cargo are poorly characterized, because techniques for distinguishing between exosomal proteins and proteins in the targeted tissues are lacking. Here, we report the development of an

Indexed as

bioorthogonal labelingcardiac ischemiaclick reactionexosomesextracellular vesiclesmesenchymal stem cells

Identifiers

PMID33898459
PMCPMC8058422
OpenAlexW3148280740

What OpenQuestion holds

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LicenceCC BY
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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.