Evidence map›Paper›PMID 38938916›Full record

ArticleJournal of extracellular biology2023

Equine mesenchymal stem cell derived extracellular vesicle immunopathology biomarker discovery.

David E Reynolds, Phoebe Vallapureddy, Renee-Tyler T Morales, Daniel Oh, Menghan Pan, Uday Chintapula, Renata L Linardi, Angela M Gaesser, Kyla Ortved, Jina Ko

Erratum issuedAbstract read
In one paragraph

Article in Journal of extracellular biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Double Digital Assay for Single Extracellular Vesicle and Single Molecule Detection.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

David E ReynoldsDepartment of Bioengineering University of Pennsylvania Philadelphia Pennsylvania USA.
Phoebe VallapureddyDepartment of Bioengineering University of Pennsylvania Philadelphia Pennsylvania USA.
Renee-Tyler T MoralesDepartment of Bioengineering University of Pennsylvania Philadelphia Pennsylvania USA.
Daniel OhDepartment of Bioengineering University of Pennsylvania Philadelphia Pennsylvania USA.
Menghan PanDepartment of Bioengineering University of Pennsylvania Philadelphia Pennsylvania USA.
Uday ChintapulaDepartment of Bioengineering University of Pennsylvania Philadelphia Pennsylvania USA.
Renata L LinardiDepartment of Clinical Studies New Bolton Center, School of Veterinary Medicine, University of Pennsylvania Philadelphia Pennsylvania USA.
Angela M GaesserDepartment of Clinical Studies New Bolton Center, School of Veterinary Medicine, University of Pennsylvania Philadelphia Pennsylvania USA.
Kyla OrtvedDepartment of Clinical Studies New Bolton Center, School of Veterinary Medicine, University of Pennsylvania Philadelphia Pennsylvania USA.
Jina KoDepartment of Bioengineering University of Pennsylvania Philadelphia Pennsylvania USA.ORCID https://orcid.org/0000-0002-4941-4234

Funding

Mapping Single Extracellular Vesicles to Parent Cells for Immunotherapy MonitoringR00CA256353 · NCI · UNIVERSITY OF PENNSYLVANIA · PI KO, JINA · 2022 to 2024
$741k
NCI NIH HHS R00 CA256353
6 · The paper itself

Abstract

The use of mesenchymal stem cells (MSCs) in human and veterinary clinical applications has become a subject of increasing importance due to their roles in immunomodulation and regenerative processes. MSCs are especially relevant in equine medicine because they may have the ability to treat prevalent musculoskeletal disorders, among other conditions. However, recent evidence suggests that the components secreted by MSCs, particularly extracellular vesicles (EVs), are responsible for these properties. EVs contain proteins and nucleic acids, which possess an active role in intercellular communication and can be used as therapeutics. However, because the intersection of equine veterinary medicine with EVs remains a relatively new field, there is a demand to identify biomarkers that can discern and enrich for therapeutic EVs, progressing their clinical efficacy. In this study, we identified and characterized 84 miRNAs, between three equine donors involved in immunomodulation in cell and EV subjects. We discovered distinct groups of shared miRNAs, like miR-21-5p and miR-451a, that are abundant and enriched between the donors' EVs, respectively. By mapping and comparing the MSC-EV miRNA expression, we discovered many pathways that are involved in immunomodulation and tissue regenerative processes related to equine clinical applications. Therefore, the miRNAs highlighted in this article can be used as valuable biomarkers for screening MSC-derived EVs for potential equine therapy.

Indexed as

biomarker discoveryequineextracellular vesicleimmunomodulationmesenchymal stem celltherapeutic

Identifiers

PMID38938916
PMCPMC11080797

What OpenQuestion holds

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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.