دورية أكاديمية

Engineered EVs for Oxidative Stress Protection

التفاصيل البيبلوغرافية
العنوان: Engineered EVs for Oxidative Stress Protection
المؤلفون: Anna Maria Tolomeo, Santina Quarta, Alessandra Biasiolo, Mariagrazia Ruvoletto, Michela Pozzobon, Giada De Lazzari, Ricardo Malvicini, Cristian Turato, Giorgio Arrigoni, Patrizia Pontisso, Maurizio Muraca
المصدر: Pharmaceuticals, Vol 14, Iss 8, p 703 (2021)
بيانات النشر: MDPI AG, 2021.
سنة النشر: 2021
المجموعة: LCC:Medicine
LCC:Pharmacy and materia medica
مصطلحات موضوعية: extracellular vesicles, SerpinB3, oxidative stress, cytoprotection, Medicine, Pharmacy and materia medica, RS1-441
الوصف: Extracellular vesicles (EVs) are increasingly studied as vectors for drug delivery because they can transfer a variety of molecules across biological barriers. SerpinB3 is a serine protease inhibitor that has shown a protective anti-apoptotic function in a variety of stressful conditions. The aim of this study was to evaluate protection from oxidative stress-induced damage, using extracellular vesicles that overexpress SerpinB3 (EVs-SB3) in order to enhance the effect of extracellular vesicles on cellular homeostasis. EVs-SB3s were obtained from HepG2 cells engineered to overexpress SerpinB3 and they revealed significant proteomic changes, mostly characterized by a reduced expression of other proteins compared with EVs from non-engineered cells. These EV preparations showed a significantly higher protection from H2O2 induced oxidative stress in both the hepatoma cell line and in primary cardiomyocytes, compared to cells treated with naïve EVs or SerpinB3 alone, used at the same concentration. In conclusion, the induction of SerpinB3 transgene expression results in the secretion of EVs enriched with the protein product that exhibits enhanced cytoprotective activity, compared with naïve EVs or the nude SerpinB3 protein.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1424-8247
Relation: https://www.mdpi.com/1424-8247/14/8/703; https://doaj.org/toc/1424-8247
DOI: 10.3390/ph14080703
URL الوصول: https://doaj.org/article/7e84797b475a443e8b4f24d7cedbd8e0
رقم الأكسشن: edsdoj.7e84797b475a443e8b4f24d7cedbd8e0
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14248247
DOI:10.3390/ph14080703