Microvesicles derived from dermal myofibroblasts modify the integrity of the blood and lymphatic barriers using distinct endocytosis pathways.

blood endothelial cells endothelial barrier endothelial cell extracellular vesicles lymphatic endothelial cells microvesicles myofibroblast regeneration

Journal

Journal of extracellular biology
ISSN: 2768-2811
Titre abrégé: J Extracell Biol
Pays: United States
ID NLM: 9918382980506676

Informations de publication

Date de publication:
May 2024
Historique:
received: 10 08 2023
revised: 06 02 2024
accepted: 15 04 2024
medline: 28 6 2024
pubmed: 28 6 2024
entrez: 28 6 2024
Statut: epublish

Résumé

Microvesicles (MVs) are a subtype of extracellular vesicles that can transfer biological information from their producer cells to target cells. This communication can in turn affect both normal and pathological processes. Mounting evidence has revealed that dermal wound myofibroblasts (Wmyo) produce MVs, which can transfer biomolecules impacting receptor cells such as human dermal microvascular endothelial cells (HDMECs). While the effects of MVs on HDMECs are generally well described in the literature, little is known about the transport of MVs across the HDMEC barrier, and their potential effect on the barrier integrity remains unknown. Here, we investigated these roles of Wmyo-derived MVs on two sub-populations of HDMECs, blood endothelial cells (BECs) and lymphatic endothelial cells (LECs). Using an in vitro model to mimic the endothelial barrier, we showed that MVs crossed the LEC barrier but not the BEC barrier. In addition, we demonstrated that MVs were able to influence the cell-cell junctions of HDMECs. Specifically, we observed that after internalization via the predominantly caveolin-dependent pathway, MVs induced the opening of junctions in BECs. Conversely, in LECs, MVs mainly use the macropinocytosis pathway and induce closure of these junctions. Moreover, proteins in the MV membrane were responsible for this effect, but not specifically those belonging to the VEGF family. Finally, we found that once the LEC barrier permeability was reduced by MV stimuli, MVs ceased to cross the barrier. Conversely, when the BEC barrier was rendered permeable following stimulation with MVs, they were subsequently able to cross the barrier via the paracellular pathway. Taken together, these results suggest that the study of Wmyo-derived MVs offers valuable insights into their interaction with the HDMEC barrier in the context of wound healing. They highlight the potential significance of these MVs in the overall process.

Identifiants

pubmed: 38939570
doi: 10.1002/jex2.151
pii: JEX2151
pmc: PMC11080715
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e151

Informations de copyright

© 2024 The Authors. Journal of Extracellular Biology published by Wiley Periodicals LLC on behalf of International Society for Extracellular Vesicles.

Déclaration de conflit d'intérêts

The authors report no conflict of interests.

Auteurs

Syrine Arif (S)

Centre de recherche en organogénèse expérimentale de l'Université Laval/LOEX Centre de recherche du CHU de Québec-Université Laval Quebec Canada.

Megan Richer (M)

Centre de recherche en organogénèse expérimentale de l'Université Laval/LOEX Centre de recherche du CHU de Québec-Université Laval Quebec Canada.

Sébastien Larochelle (S)

Centre de recherche en organogénèse expérimentale de l'Université Laval/LOEX Centre de recherche du CHU de Québec-Université Laval Quebec Canada.

Véronique J Moulin (VJ)

Centre de recherche en organogénèse expérimentale de l'Université Laval/LOEX Centre de recherche du CHU de Québec-Université Laval Quebec Canada.
Department of Surgery, Faculty of Medicine Université Laval Quebec Canada.

Classifications MeSH