Assessment of the structural and functional characteristics of human mesenchymal stem cells associated with a prolonged exposure of morphine

Abstract The discovery of the expression of opioid receptors in the skin and their role in orchestrating the process of tissue repair gave rise to questions regarding the potential effects of clinical morphine treatment in wound healing. Although short term treatment was reported to improve tissue r...

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Autores principales: Francesco Carano, Gabriella Teti, Alessandra Ruggeri, Francesca Chiarini, Arianna Giorgetti, Maria C. Mazzotti, Paolo Fais, Mirella Falconi
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/137e05914bf043ada2750a0bf2e6a58f
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spelling oai:doaj.org-article:137e05914bf043ada2750a0bf2e6a58f2021-12-02T17:37:11ZAssessment of the structural and functional characteristics of human mesenchymal stem cells associated with a prolonged exposure of morphine10.1038/s41598-021-98682-62045-2322https://doaj.org/article/137e05914bf043ada2750a0bf2e6a58f2021-09-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-98682-6https://doaj.org/toc/2045-2322Abstract The discovery of the expression of opioid receptors in the skin and their role in orchestrating the process of tissue repair gave rise to questions regarding the potential effects of clinical morphine treatment in wound healing. Although short term treatment was reported to improve tissue regeneration, in vivo chronic administration was associated to an impairment of the physiological healing process and systemic fibrosis. Human mesenchymal stem cells (hMSCs) play a fundamental role in tissue regeneration. In this regard, acute morphine exposition was recently reported to impact negatively on the functional characteristics of hMSCs, but little is currently known about its long-term effects. To determine how a prolonged treatment could impair their functional characteristics, we exposed hMSCs to increasing morphine concentrations respectively for nine and eighteen days, evaluating in particular the fibrogenic potential exerted by the long-term exposition. Our results showed a time dependent cell viability decline, and conditions compatible with a cellular senescent state. Ultrastructural and protein expression analysis were indicative of increased autophagy, suggesting a relation to a detoxification activity. In addition, the enhanced transcription observed for the genes involved in the synthesis and regulation of type I collagen suggested the possibility that a prolonged morphine treatment might exert its fibrotic potential risk, even involving the hMSCs.Francesco CaranoGabriella TetiAlessandra RuggeriFrancesca ChiariniArianna GiorgettiMaria C. MazzottiPaolo FaisMirella FalconiNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Francesco Carano
Gabriella Teti
Alessandra Ruggeri
Francesca Chiarini
Arianna Giorgetti
Maria C. Mazzotti
Paolo Fais
Mirella Falconi
Assessment of the structural and functional characteristics of human mesenchymal stem cells associated with a prolonged exposure of morphine
description Abstract The discovery of the expression of opioid receptors in the skin and their role in orchestrating the process of tissue repair gave rise to questions regarding the potential effects of clinical morphine treatment in wound healing. Although short term treatment was reported to improve tissue regeneration, in vivo chronic administration was associated to an impairment of the physiological healing process and systemic fibrosis. Human mesenchymal stem cells (hMSCs) play a fundamental role in tissue regeneration. In this regard, acute morphine exposition was recently reported to impact negatively on the functional characteristics of hMSCs, but little is currently known about its long-term effects. To determine how a prolonged treatment could impair their functional characteristics, we exposed hMSCs to increasing morphine concentrations respectively for nine and eighteen days, evaluating in particular the fibrogenic potential exerted by the long-term exposition. Our results showed a time dependent cell viability decline, and conditions compatible with a cellular senescent state. Ultrastructural and protein expression analysis were indicative of increased autophagy, suggesting a relation to a detoxification activity. In addition, the enhanced transcription observed for the genes involved in the synthesis and regulation of type I collagen suggested the possibility that a prolonged morphine treatment might exert its fibrotic potential risk, even involving the hMSCs.
format article
author Francesco Carano
Gabriella Teti
Alessandra Ruggeri
Francesca Chiarini
Arianna Giorgetti
Maria C. Mazzotti
Paolo Fais
Mirella Falconi
author_facet Francesco Carano
Gabriella Teti
Alessandra Ruggeri
Francesca Chiarini
Arianna Giorgetti
Maria C. Mazzotti
Paolo Fais
Mirella Falconi
author_sort Francesco Carano
title Assessment of the structural and functional characteristics of human mesenchymal stem cells associated with a prolonged exposure of morphine
title_short Assessment of the structural and functional characteristics of human mesenchymal stem cells associated with a prolonged exposure of morphine
title_full Assessment of the structural and functional characteristics of human mesenchymal stem cells associated with a prolonged exposure of morphine
title_fullStr Assessment of the structural and functional characteristics of human mesenchymal stem cells associated with a prolonged exposure of morphine
title_full_unstemmed Assessment of the structural and functional characteristics of human mesenchymal stem cells associated with a prolonged exposure of morphine
title_sort assessment of the structural and functional characteristics of human mesenchymal stem cells associated with a prolonged exposure of morphine
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/137e05914bf043ada2750a0bf2e6a58f
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