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Regenerative treatment using a radioelectric asymmetric conveyor as a novel tool in antiaging medicine: an in vitro beta-galactosidase study
BACKGROUND: Beta-galactosidase is the most widely used biomarker for highlighting the processes of cellular aging, including neurodegeneration. On this basis, we decided to test in vitro whether a set of rescuing/reparative events previously observed by us in subjects treated with radioelectric asym...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3396051/ https://www.ncbi.nlm.nih.gov/pubmed/22807628 http://dx.doi.org/10.2147/CIA.S33312 |
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author | Rinaldi, Salvatore Maioli, Margherita Santaniello, Sara Castagna, Alessandro Pigliaru, Gianfranco Gualini, Sara Margotti, Matteo Lotti Carta, Arturo Fontani, Vania Ventura, Carlo |
author_facet | Rinaldi, Salvatore Maioli, Margherita Santaniello, Sara Castagna, Alessandro Pigliaru, Gianfranco Gualini, Sara Margotti, Matteo Lotti Carta, Arturo Fontani, Vania Ventura, Carlo |
author_sort | Rinaldi, Salvatore |
collection | PubMed |
description | BACKGROUND: Beta-galactosidase is the most widely used biomarker for highlighting the processes of cellular aging, including neurodegeneration. On this basis, we decided to test in vitro whether a set of rescuing/reparative events previously observed by us in subjects treated with radioelectric asymmetric conveyor (REAC) technology may also involve antagonism of a marker of aging-related degenerative processes, as assessed by a reduction in beta-galactosidase at the cellular level. METHODS: Human adipose-derived stem cells were cultured at different passages, ranging from 5 to 20, with or without REAC exposure for 12 hours. The cells were then processed for biochemical beta-galactosidase staining and morphological microscopy analysis. RESULTS: We observed a significant reduction in expression of senescence associated-beta-galactosidase, and a persistence of fibroblast-like morphology typical of human adipose-derived stem cells, even at late passages. CONCLUSION: Our results indicate the ability of REAC technology to counteract in vitro senescence of human adipose-derived stem cells, and prompt the hypothesis that such technology may be exploited to antagonize in vivo senescence of tissue-resident or transplanted stem cells playing an important role in clinical treatment of age-related processes. |
format | Online Article Text |
id | pubmed-3396051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33960512012-07-17 Regenerative treatment using a radioelectric asymmetric conveyor as a novel tool in antiaging medicine: an in vitro beta-galactosidase study Rinaldi, Salvatore Maioli, Margherita Santaniello, Sara Castagna, Alessandro Pigliaru, Gianfranco Gualini, Sara Margotti, Matteo Lotti Carta, Arturo Fontani, Vania Ventura, Carlo Clin Interv Aging Original Research BACKGROUND: Beta-galactosidase is the most widely used biomarker for highlighting the processes of cellular aging, including neurodegeneration. On this basis, we decided to test in vitro whether a set of rescuing/reparative events previously observed by us in subjects treated with radioelectric asymmetric conveyor (REAC) technology may also involve antagonism of a marker of aging-related degenerative processes, as assessed by a reduction in beta-galactosidase at the cellular level. METHODS: Human adipose-derived stem cells were cultured at different passages, ranging from 5 to 20, with or without REAC exposure for 12 hours. The cells were then processed for biochemical beta-galactosidase staining and morphological microscopy analysis. RESULTS: We observed a significant reduction in expression of senescence associated-beta-galactosidase, and a persistence of fibroblast-like morphology typical of human adipose-derived stem cells, even at late passages. CONCLUSION: Our results indicate the ability of REAC technology to counteract in vitro senescence of human adipose-derived stem cells, and prompt the hypothesis that such technology may be exploited to antagonize in vivo senescence of tissue-resident or transplanted stem cells playing an important role in clinical treatment of age-related processes. Dove Medical Press 2012 2012-06-29 /pmc/articles/PMC3396051/ /pubmed/22807628 http://dx.doi.org/10.2147/CIA.S33312 Text en © 2012 Rinaldi et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Rinaldi, Salvatore Maioli, Margherita Santaniello, Sara Castagna, Alessandro Pigliaru, Gianfranco Gualini, Sara Margotti, Matteo Lotti Carta, Arturo Fontani, Vania Ventura, Carlo Regenerative treatment using a radioelectric asymmetric conveyor as a novel tool in antiaging medicine: an in vitro beta-galactosidase study |
title | Regenerative treatment using a radioelectric asymmetric conveyor as a novel tool in antiaging medicine: an in vitro beta-galactosidase study |
title_full | Regenerative treatment using a radioelectric asymmetric conveyor as a novel tool in antiaging medicine: an in vitro beta-galactosidase study |
title_fullStr | Regenerative treatment using a radioelectric asymmetric conveyor as a novel tool in antiaging medicine: an in vitro beta-galactosidase study |
title_full_unstemmed | Regenerative treatment using a radioelectric asymmetric conveyor as a novel tool in antiaging medicine: an in vitro beta-galactosidase study |
title_short | Regenerative treatment using a radioelectric asymmetric conveyor as a novel tool in antiaging medicine: an in vitro beta-galactosidase study |
title_sort | regenerative treatment using a radioelectric asymmetric conveyor as a novel tool in antiaging medicine: an in vitro beta-galactosidase study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3396051/ https://www.ncbi.nlm.nih.gov/pubmed/22807628 http://dx.doi.org/10.2147/CIA.S33312 |
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