作者: Hussain Md Shahjalal , Nobuaki Shiraki , Daisuke Sakano , Kazuhide Kikawa , Soichiro Ogaki
DOI: 10.1093/JMCB/MJU029
关键词: Cell therapy 、 Cell biology 、 Internal medicine 、 Progenitor cell 、 Cellular differentiation 、 Induced pluripotent stem cell 、 Pancreas 、 Noggin 、 Chemistry 、 Insulin 、 Endocrinology 、 PDX1
摘要: Human induced pluripotent stem (hiPS) cells are considered a potential source for the generation of insulin-producing pancreatic β-cells because their differentiation capacity. In this study, we have developed five-step xeno-free culture system to efficiently differentiate hiPS into in vitro. We found that high NOGGIN concentration is crucial specifically inducing first and duodenal homeobox-1 (PDX1)-positive progenitors then neurogenin 3 (NGN3)-expressing endocrine progenitors, while suppressing hepatic or intestinal cells. also combination 3-isobutyl-1-methylxanthine (IBMX), exendin-4, nicotinamide was important insulin single-positive expressed various β-cell markers. Most notably, differentiated contained endogenous C-peptide pools were released response secretagogues levels glucose. Therefore, our results demonstrate feasibility generating hiPS-derived under conditions highlight treat patients with type 1 diabetes.