کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5517000 1543037 2017 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The impact of oxidative DNA changes and ATM expression on morphological and functional activities on hepatocytes obtained from mesenchymal stem cells
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیوشیمی، ژنتیک و زیست شناسی مولکولی (عمومی)
پیش نمایش صفحه اول مقاله
The impact of oxidative DNA changes and ATM expression on morphological and functional activities on hepatocytes obtained from mesenchymal stem cells
چکیده انگلیسی


• Hepatogenic differentiation of MSCs is associated with changes in ROS and DNA adducts (8-OH-dG).
• Changes in ROS and 8-OH-dG is associated with changes in nuclear/cytoplasmic ATM expression.
• Hepatocytes derived from MSCs were normal, although there was signs of oxidative damage.

Resistance to oxidative damages in undifferentiated mesenchymal stem cells (MSCs) in comparison with the undifferentiated progenitor cells may differ depending on several factors. This study was carried out to examine the impact of hepatogenic differentiation process of MSCs on oxidative DNA damage markers. Hepatic differentiation of MSCs was carried out using a two-step conventional protocol and the cells were processed for characterization using morphological and biochemical markers. During the course of differentiation cellular levels of reactive oxygen species (ROS), 8-hydroxy-2'-deoxyguanosine (8-OH-dG) and expression of ataxia-telangiectasia mutated (ATM) protein were estimated at time intervals (10, 20 and 30 days). The results showed a decrease in cellular ROS (13%, P < 0.05) at early stages of hepatogenic differentiation. Similarly, there was a small but significant decrease in 8-OH-dG level and ATM expression in differentiated hepatocytes. Despite the small changes in oxidative damage factors and ATM expression during the differentiation process, the hepatocytes obtained were morphologically and biologically intact.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biologicals - Volume 47, May 2017, Pages 52–58