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Wissenschaftliche Publikation

Extracellular Vesicles in Human Skin: Cross-Talk from Senescent Fibroblasts to Keratinocytes by miRNAs.

Publikation aus Health
Biomedizinische Gewebe Monitoring

Terlecki-Zaniewicz, Lucia, Vera Pils, Madhusudhan Reddy Bobbili, Ingo Lämmermann, Ida Perrotta, Tonja Grillenberger, Jennifer Schwestka, Katrin Weiß, Dietmar Pum, Elsa Arcalis, Simon Schwingenschuh, Thomas Birngruber, Marlene Brandstetter, Thomas Heuser, Markus Schosserer, Frederique Morizot, Michael Mildner, Eva Stöger, Erwin Tschachler, Regina Weinmüllner, Florian Gruber, Johannes Grillari

Journal of Investigative Dermatology , 6/2019

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.

Keywords: ermal open flow microperfusion

Url: https://www.ncbi.nlm.nih.gov/pubmed/31220456