دورية أكاديمية

Glucose-Induced Oxidative Stress Reduces Proliferation in Embryonic Stem Cells via FOXO3A/β-Catenin-Dependent Transcription of p21cip1

التفاصيل البيبلوغرافية
العنوان: Glucose-Induced Oxidative Stress Reduces Proliferation in Embryonic Stem Cells via FOXO3A/β-Catenin-Dependent Transcription of p21cip1
المؤلفون: Darcie L. McClelland Descalzo, Tiffany S. Satoorian, Lauren M. Walker, Nicole R.L. Sparks, Polina Y. Pulyanina, Nicole I. zur Nieden
المصدر: Stem Cell Reports, Vol 7, Iss 1, Pp 55-68 (2016)
بيانات النشر: Elsevier, 2016.
سنة النشر: 2016
المجموعة: LCC:Medicine (General)
LCC:Biology (General)
مصطلحات موضوعية: glucose, oxidative stress, proliferation, FOXO, β-catenin, embryonic stem cell, metabolism, AKT, c-jun kinase, Medicine (General), R5-920, Biology (General), QH301-705.5
الوصف: Embryonic stem cells (ESCs), which are derived from a peri-implantation embryo, are routinely cultured in medium containing diabetic glucose (Glc) concentrations. While pregnancy in women with pre-existing diabetes may result in small embryos, whether such high Glc levels affect ESC growth remains uncovered. We show here that long-term exposure of ESCs to diabetic Glc inhibits their proliferation, thereby mimicking in vivo findings. Molecularly, Glc exposure increased oxidative stress and activated Forkhead box O3a (FOXO3a), promoting increased expression and activity of the ROS-removal enzymes superoxide dismutase and catalase and the cell-cycle inhibitors p21cip1 and p27kip1. Diabetic Glc also promoted β-catenin nuclear localization and the formation of a complex with FOXO3a that localized to the promoters of Sod2, p21cip1, and potentially p27kip1. Our results demonstrate an adaptive response to increases in oxidative stress induced by diabetic Glc conditions that promote ROS removal, but also result in a decrease in proliferation.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2213-6711
Relation: http://www.sciencedirect.com/science/article/pii/S2213671116300984; https://doaj.org/toc/2213-6711
DOI: 10.1016/j.stemcr.2016.06.006
URL الوصول: https://doaj.org/article/155d41934c0443c89ac18925c8299cc8
رقم الأكسشن: edsdoj.155d41934c0443c89ac18925c8299cc8
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:22136711
DOI:10.1016/j.stemcr.2016.06.006