| Literature DB >> 33255167 |
Emanuela Bellu1, Giuseppe Garroni1, Sara Cruciani1, Francesca Balzano1, Diletta Serra1, Rosanna Satta2, Maria Antonia Montesu2, Angela Fadda3, Maurizio Mulas4, Giorgia Sarais5, Pasquale Bandiera1, Elena Torreggiani6, Fernanda Martini6, Mauro Tognon6, Carlo Ventura7, Jiří Beznoska8, Evzen Amler8,9, Margherita Maioli1,10,11.
Abstract
Natural cosmetic products have recently re-emerged as a novel tool able to counteract skin aging and skin related damages. In addition, recently achieved progress in nanomedicine opens a novel approach yielding from combination of modern nanotechnology with traditional treatment for innovative pharmacotherapeutics. In the present study, we investigated the antiaging effect of a pretreatment with Myrtus communis natural extract combined with a polycaprolactone nanofibrous scaffold (NanoPCL-M) on skin cell populations exposed to UV. We set up a novel model of skin on a bioreactor mimicking a crosstalk between keratinocytes, stem cells and fibroblasts, as in skin. Beta-galactosidase assay, indicating the amount of senescent cells, and viability assay, revealed that fibroblasts and stem cells pretreated with NanoPCL-M and then exposed to UV are superimposable to control cells, untreated and unexposed to UV damage. On the other hand, cells only exposed to UV stress, without NanoPCL-M pretreatment, exhibited a significantly higher yield of senescent elements. Keratinocyte-based 3D structures appeared disjointed after UV-stress, as compared to NanoPCL-M pretreated samples. Gene expression analysis performed on different senescence associated genes, revealed the activation of a molecular program of rejuvenation in stem cells pretreated with NanoPCL-M and then exposed to UV. Altogether, our results highlight a future translational application of NanoPCL-M to prevent skin aging.Entities:
Keywords: 4D dynamic model; biophysics; cell senescence; cellular mechanisms; nanofibers; natural extracts; precision medicine; skin aging; stem cells
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Year: 2020 PMID: 33255167 PMCID: PMC7760051 DOI: 10.3390/cells9122530
Source DB: PubMed Journal: Cells ISSN: 2073-4409 Impact factor: 6.600