Evidence map›Paper›PMID 37443741›Full record

ArticleCells2023

Microvesicle-Mediated Tissue Regeneration Mitigates the Effects of Cellular Ageing.

Nikolaos Panagiotou, Dagmara McGuinness, Armand M G Jaminon, Barend Mees, Colin Selman, Leon Schurgers, Paul G Shiels

Open access · goldAbstract read
In one paragraph

Article in Cells, 2023. 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 74% 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, 0 citations in OpenAlex.

  1. 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

7 authors at 3 institutions in 3 countries.

Nikolaos PanagiotouDavidson Building, School of Molecular Biosciences, University of Glasgow, Glasgow G12 8QQ, UK;nikos.panagiotou@theracell.eu (N.P.).ORCID 0000-0003-3157-3285
Dagmara McGuinnessSchool of Infection & Immunity, University of Glasgow, Glasgow G12 8QQ, UK.ORCID 0000-0001-9057-3504
Armand M G JaminonDepartment of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, 6229 ER Maastricht, NetherlandsThe Netherlands.ORCID 0000-0002-1844-2363
Barend MeesDepartment of Vascular Surgery, Maastricht University Medical Centre (MUMC), Maastricht, The Netherlands.
Colin SelmanGraham Kerr Building, College of Medical, Veterinary & Life Sciences, Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow G12 8QQ, UK.
Leon SchurgersDepartment of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, 6229 ER Maastricht, NetherlandsThe Netherlands.ORCID 0000-0001-7867-6957
Paul G ShielsDavidson Building, School of Molecular Biosciences, University of Glasgow, Glasgow G12 8QQ, UK;nikos.panagiotou@theracell.eu (N.P.).
University of Glasgow · GBMaastricht University · NLMaastricht University Medical Centre · NL

Funding

Biotechnology and Biological Sciences Research Council DTP Studentship for NP, to PS, CS
6 · The paper itself

Abstract

Extracellular vesicles (EVs), comprising microvesicles (MVs) and exosomes (Exos), are membranous vesicles secreted by cells which mediate the repair of cellular and tissue damage via paracrine mechanisms. The action of EVs under normative and morbid conditions in the context of ageing remains largely unexplored. We demonstrate that MVs, but not Exos, from Pathfinder cells (PCs), a putative stem cell regulatory cell type, enhance the repair of human dermal fibroblast (HDF) and mesenchymal stem cell (MSC) co-cultures, following both mechanical and genotoxic stress. Critically, this effect was found to be both cellular age and stress specific. Notably, MV treatment was unable to repair mechanical injury in older co-cultures but remained therapeutic following genotoxic stress. These observations were further confirmed in human dermal fibroblast (HDF) and vascular smooth muscle cell (VSMC) co-cultures of increasing cellular age. In a model of comorbidity comprising co-cultures of HDFs and highly senescent abdominal aortic aneurysm (AAA) VSMCs, MV administration appeared to be senotherapeutic, following both mechanical and genotoxic stress. Our data provide insights into EVs and the specific roles they play during tissue repair and ageing. These data will potentiate the development of novel cell-free therapeutic interventions capable of attenuating age-associated morbidities and avoiding undesired effects.

Indexed as

Cell-Derived MicroparticlesExosomesExtracellular VesiclesAgedCellular SenescenceHumansWound Healingageingexosomesextracellular vesiclesmicrovesiclesregenerative medicinestem cellswound healing

Identifiers

PMID37443741
PMCPMC10340655
OpenAlexW4382136823

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.