Cell-surface markers for the isolation of pancreatic cell types derived from human embryonic stem cells |
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Authors: | Kelly Olivia G Chan Man Yin Martinson Laura A Kadoya Kuniko Ostertag Traci M Ross Kelly G Richardson Mike Carpenter Melissa K D'Amour Kevin A Kroon Evert Moorman Mark Baetge Emmanuel E Bang Anne G |
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Affiliation: | ViaCyte, Inc. (formerly Novocell, Inc.), San Diego, California, USA. okelly@viacyte.com |
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Abstract: | Using a flow cytometry-based screen of commercial antibodies, we have identified cell-surface markers for the separation of pancreatic cell types derived from human embryonic stem (hES) cells. We show enrichment of pancreatic endoderm cells using CD142 and of endocrine cells using CD200 and CD318. After transplantation into mice, enriched pancreatic endoderm cells give rise to all the pancreatic lineages, including functional insulin-producing cells, demonstrating that they are pancreatic progenitors. In contrast, implanted, enriched polyhormonal endocrine cells principally give rise to glucagon cells. These antibodies will aid investigations that use pancreatic cells generated from pluripotent stem cells to study diabetes and pancreas biology. |
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