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Moringin Pretreatment Inhibits the Expression of Genes Involved in Mitophagy in the Stem Cell of the Human Periodontal Ligament

Moringin [4-(α-L-rhamnosyloxy) benzyl isothiocyanate] is an isothiocyanate extracted from Moringa oleifera seeds. It is an antioxidant known for several biological properties useful in the treatment of neurodegenerative diseases. Several neurodegenerative disorders such as Parkinson’s and Alzheimer’...

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Autores principales: Chiricosta, Luigi, Gugliandolo, Agnese, Diomede, Francesca, Pizzicannella, Jacopo, Trubiani, Oriana, Iori, Renato, Tardiolo, Giuseppe, Guarnieri, Simone, Bramanti, Placido, Mazzon, Emanuela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767209/
https://www.ncbi.nlm.nih.gov/pubmed/31487916
http://dx.doi.org/10.3390/molecules24183217
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author Chiricosta, Luigi
Gugliandolo, Agnese
Diomede, Francesca
Pizzicannella, Jacopo
Trubiani, Oriana
Iori, Renato
Tardiolo, Giuseppe
Guarnieri, Simone
Bramanti, Placido
Mazzon, Emanuela
author_facet Chiricosta, Luigi
Gugliandolo, Agnese
Diomede, Francesca
Pizzicannella, Jacopo
Trubiani, Oriana
Iori, Renato
Tardiolo, Giuseppe
Guarnieri, Simone
Bramanti, Placido
Mazzon, Emanuela
author_sort Chiricosta, Luigi
collection PubMed
description Moringin [4-(α-L-rhamnosyloxy) benzyl isothiocyanate] is an isothiocyanate extracted from Moringa oleifera seeds. It is an antioxidant known for several biological properties useful in the treatment of neurodegenerative diseases. Several neurodegenerative disorders such as Parkinson’s and Alzheimer’s diseases are linked to dysfunctional mitochondria due to the resulting increase of Reactive Oxygen Species (ROS). Stem cell-based therapeutic treatments in neurodegenerative diseases provide an alternative strategy aimed to replace the impaired tissue. In this study were investigated the deregulated genes involved in mitophagy in the human periodontal ligament stem cells pretreated with moringin. The RNA-seq study reveals the downregulation of PINK1, with a fold change (FC) of −0.56, such as the genes involved in the phagophore formation (MAP1LC3B FC: −0.73, GABARAP FC: −0.52, GABARAPL1 FC: −0.70, GABARAPL2 FC: −0.39). The moringin pretreatment downregulates the pro−apoptotic gene BAX (−0.66) and upregulates the anti-apoptotic genes BCL2L12 (FC: 1.35) and MCL1 (FC: 0.36). The downregulation of the most of the caspases (CASP1 FC: −1.43, CASP4 FC: −0.18, CASP6 FC: −1.34, CASP7 FC: −0.46, CASP8 FC: −0.65) implies the inactivation of the apoptotic process. Our results suggest that mitochondrial dysfunctions induced by oxidative stress can be inhibited by moringin pretreatment in human periodontal ligament stem cells (hPDLSCs).
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spelling pubmed-67672092019-10-02 Moringin Pretreatment Inhibits the Expression of Genes Involved in Mitophagy in the Stem Cell of the Human Periodontal Ligament Chiricosta, Luigi Gugliandolo, Agnese Diomede, Francesca Pizzicannella, Jacopo Trubiani, Oriana Iori, Renato Tardiolo, Giuseppe Guarnieri, Simone Bramanti, Placido Mazzon, Emanuela Molecules Article Moringin [4-(α-L-rhamnosyloxy) benzyl isothiocyanate] is an isothiocyanate extracted from Moringa oleifera seeds. It is an antioxidant known for several biological properties useful in the treatment of neurodegenerative diseases. Several neurodegenerative disorders such as Parkinson’s and Alzheimer’s diseases are linked to dysfunctional mitochondria due to the resulting increase of Reactive Oxygen Species (ROS). Stem cell-based therapeutic treatments in neurodegenerative diseases provide an alternative strategy aimed to replace the impaired tissue. In this study were investigated the deregulated genes involved in mitophagy in the human periodontal ligament stem cells pretreated with moringin. The RNA-seq study reveals the downregulation of PINK1, with a fold change (FC) of −0.56, such as the genes involved in the phagophore formation (MAP1LC3B FC: −0.73, GABARAP FC: −0.52, GABARAPL1 FC: −0.70, GABARAPL2 FC: −0.39). The moringin pretreatment downregulates the pro−apoptotic gene BAX (−0.66) and upregulates the anti-apoptotic genes BCL2L12 (FC: 1.35) and MCL1 (FC: 0.36). The downregulation of the most of the caspases (CASP1 FC: −1.43, CASP4 FC: −0.18, CASP6 FC: −1.34, CASP7 FC: −0.46, CASP8 FC: −0.65) implies the inactivation of the apoptotic process. Our results suggest that mitochondrial dysfunctions induced by oxidative stress can be inhibited by moringin pretreatment in human periodontal ligament stem cells (hPDLSCs). MDPI 2019-09-04 /pmc/articles/PMC6767209/ /pubmed/31487916 http://dx.doi.org/10.3390/molecules24183217 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chiricosta, Luigi
Gugliandolo, Agnese
Diomede, Francesca
Pizzicannella, Jacopo
Trubiani, Oriana
Iori, Renato
Tardiolo, Giuseppe
Guarnieri, Simone
Bramanti, Placido
Mazzon, Emanuela
Moringin Pretreatment Inhibits the Expression of Genes Involved in Mitophagy in the Stem Cell of the Human Periodontal Ligament
title Moringin Pretreatment Inhibits the Expression of Genes Involved in Mitophagy in the Stem Cell of the Human Periodontal Ligament
title_full Moringin Pretreatment Inhibits the Expression of Genes Involved in Mitophagy in the Stem Cell of the Human Periodontal Ligament
title_fullStr Moringin Pretreatment Inhibits the Expression of Genes Involved in Mitophagy in the Stem Cell of the Human Periodontal Ligament
title_full_unstemmed Moringin Pretreatment Inhibits the Expression of Genes Involved in Mitophagy in the Stem Cell of the Human Periodontal Ligament
title_short Moringin Pretreatment Inhibits the Expression of Genes Involved in Mitophagy in the Stem Cell of the Human Periodontal Ligament
title_sort moringin pretreatment inhibits the expression of genes involved in mitophagy in the stem cell of the human periodontal ligament
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767209/
https://www.ncbi.nlm.nih.gov/pubmed/31487916
http://dx.doi.org/10.3390/molecules24183217
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