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Article Publish Status: FREE
Abstract Title:

Combination of Epigallocatechin Gallate and Sulforaphane Counteracts In Vitro Oxidative Stress and Delays Stemness Loss of Amniotic Fluid Stem Cells.

Abstract Source:

Oxid Med Cell Longev. 2018 ;2018:5263985. Epub 2018 Dec 17. PMID: 30647811

Abstract Author(s):

Pasquale Marrazzo, Cristina Angeloni, Michela Freschi, Antonello Lorenzini, Cecilia Prata, Tullia Maraldi, Silvana Hrelia

Article Affiliation:

Pasquale Marrazzo

Abstract:

Amniotic fluid stem cells (AFSCs) are characterizedby a unique niche guarantying their homeostatic role in the body. Maintaining the functionality of stem cellsfor clinical applications requires a continuous improvement of cell culture conditions. Cellular redox status plays an important role in stem cell biology as long as reactive oxygen species (ROS) concentration is finely regulated and their adverse effects are excluded. The aim of this study was to investigate the protective effect of two antioxidants, sulforaphane (SF) and epigallocatechin gallate (EGCG), againstoxidative stress due to hyperoxia and freeze-thawing cycles in AFSCs. Human AFSCs were isolated and characterized from healthy subjects. Assays of metabolic function and antioxidant activity were performed to investigate the effect of SF and EGCG cotreatment on AFSCs. Real-time PCR was used to investigate the effect of the cotreatment on pluripotency, senescence, osteogenic and adipogenic markers, and antioxidant enzymes. Alkaline phosphatase assays and Alizarin Red staining were used to confirm osteogenic differentiation. The cotreatment with SF and EGCG was effective in reducing ROS production, increasing GSH levels, and enhancing the endogenous antioxidant defences through the upregulation of glutathione reductase, NAD(P)H:quinone oxidoreductase-1, and thioredoxin reductase. Intriguingly, the cotreatment sustained the stemness state by upregulating pluripotency markers such as OCT4 and NANOG. Moreover, the cotreatment influenced senescence-associated gene markers in respect to untreated cells. The cotreatment upregulated osteogenic gene markers and promoted osteogenic differentiation. SF and EGCG can be used in combination in AFSC culture as a strategy to preserve stem cell functionality.

Study Type : Human In Vitro

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