| Literature DB >> 25303535 |
Felicia W Pagliuca1, Jeffrey R Millman1, Mads Gürtler1, Michael Segel1, Alana Van Dervort1, Jennifer Hyoje Ryu1, Quinn P Peterson1, Dale Greiner2, Douglas A Melton3.
Abstract
The generation of insulin-producing pancreatic β cells from stem cells in vitro would provide an unprecedented cell source for drug discovery and cell transplantation therapy in diabetes. However, insulin-producing cells previously generated from human pluripotent stem cells (hPSC) lack many functional characteristics of bona fide β cells. Here, we report a scalable differentiation protocol that can generate hundreds of millions of glucose-responsive β cells from hPSC in vitro. These stem-cell-derived β cells (SC-β) express markers found in mature β cells, flux Ca(2+) in response to glucose, package insulin into secretory granules, and secrete quantities of insulin comparable to adult β cells in response to multiple sequential glucose challenges in vitro. Furthermore, these cells secrete human insulin into the serum of mice shortly after transplantation in a glucose-regulated manner, and transplantation of these cells ameliorates hyperglycemia in diabetic mice.Entities:
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Year: 2014 PMID: 25303535 PMCID: PMC4617632 DOI: 10.1016/j.cell.2014.09.040
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582