Microvesicle-Mediated Tissue Regeneration Mitigates the Effects of Cellular Ageing

Author:

Panagiotou Nikolaos1ORCID,McGuinness Dagmara2ORCID,Jaminon Armand M. G.3ORCID,Mees Barend4,Selman Colin5,Schurgers Leon36ORCID,Shiels Paul G.1

Affiliation:

1. Davidson Building, School of Molecular Biosciences, University of Glasgow, Glasgow G12 8QQ, UK;nikos.panagiotou@theracell.eu (N.P.)

2. School of Infection & Immunity, University of Glasgow, Glasgow G12 8QQ, UK

3. Department of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, 6229 ER Maastricht, NetherlandsThe Netherlands

4. Department of Vascular Surgery, Maastricht University Medical Centre (MUMC), Maastricht, The Netherlands

5. Graham Kerr Building, College of Medical, Veterinary & Life Sciences, Institute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow G12 8QQ, UK

6. Institute of Experimental Medicine and Systems Biology, RWTH University Hospital, Aachen, Germany

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.

Funder

Biotechnology and Biological Sciences Research Council

NHSGGC

RegMed-XB

European Union’s Horizon 2020 research and innovation Program

Publisher

MDPI AG

Subject

General Medicine

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