| Literature DB >> 31220456 |
Lucia Terlecki-Zaniewicz1, Vera Pils1, Madhusudhan Reddy Bobbili2, Ingo Lämmermann1, Ida Perrotta3, Tonja Grillenberger1, Jennifer Schwestka1, Katrin Weiß1, Dietmar Pum4, Elsa Arcalis5, Simon Schwingenschuh6, Thomas Birngruber6, Marlene Brandstetter7, Thomas Heuser8, Markus Schosserer2, Frederique Morizot9, Michael Mildner10, Eva Stöger5, Erwin Tschachler10, Regina Weinmüllner1, Florian Gruber11, Johannes Grillari12.
Abstract
Extracellular vesicles (EVs) and their miRNA cargo are intercellular communicators transmitting their pleiotropic messages between different cell types, tissues, and body fluids. Recently, they have been reported to contribute to skin homeostasis and were identified as members of the senescence-associated secretory phenotype of human dermal fibroblasts. However, the role of EV-miRNAs in paracrine signaling during skin aging is yet unclear. Here we provide evidence for the existence of small EVs in the human skin and dermal interstitial fluid using dermal open flow microperfusion and show that EVs and miRNAs are transferred from dermal fibroblasts to epidermal keratinocytes in 2D cell culture and in human skin equivalents. We further show that the transient presence of senescent fibroblast derived small EVs accelerates scratch closure of epidermal keratinocytes, whereas long-term incubation impairs keratinocyte differentiation in vitro. Finally, we identify vesicular miR-23a-3p, highly secreted by senescent fibroblasts, as one contributor of the EV-mediated effect on keratinocytes in in vitro wound healing assays. To summarize, our findings support the current view that EVs and their miRNA cargo are members of the senescence-associated secretory phenotype and, thus, regulators of human skin homeostasis during aging.Entities:
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Year: 2019 PMID: 31220456 DOI: 10.1016/j.jid.2019.05.015
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 7.590