Medical Journals

Enhanced Yield of Neuroepithelial Precursors and Midbrain-like Dopaminergic Neurons from Human Embryonic Stem Cells Using the Bone Morphogenic Protein Antagonist Noggin.

Authors:
  • Sonntag Kai-Christian
  • Pruszak Jan
  • Yoshizaki Takahito
  • van Arensbergen Joris
  • Sanchez-Pernaute Rosario
  • Isacson Ole

From: Center for Neuroregeneration Research, Udall Parkinson’s Disease Center of Excellence, McLean Hospital, Harvard Medical School, Belmont, Massachusetts 02478, USA. kai.sonntag@mclean.harvard.edu

Stem cells (Dayton, Ohio)

  • Publish Date: Feb 2007
  • ISSN: 1066-5099
  • Volume: 25
  • Issue: 2
  • Pages: 411-8
  • Medium: Print
  • Language: English
  • Citation (JAMA): Sonntag Kai-Christian, Pruszak Jan, Yoshizaki Takahito, et al. Enhanced Yield of Neuroepithelial Precursors and Midbrain-like Dopaminergic Neurons from Human Embryonic Stem Cells Using the Bone Morphogenic Protein Antagonist Noggin.. Stem Cells Feb 2007;25:411-8

Abstract

It is currently not known whether dopamine (DA) neurons derived from human embryonic stem cells (hESCs) can survive in vivo and alleviate symptoms in models of Parkinson disease (PD). Here, we report the use of Noggin (a bone morphogenic protein antagonist) to induce neuroectodermal cell development and increase the yield of DA neurons from hESCs. A combination of stromal-derived inducing activity and Noggin markedly enhanced the generation of neuroepithelial progenitors that could give rise to DA neurons. In addition, Noggin diminished the occurrence of a fibroblast-like Nestin-positive precursor population that differentiated into myocytes. After transplantation of differentiated hESCs to a rodent model of PD, some grafts contained human midbrain-like DA neurons. This protocol demonstrates hESC derivation and survival of human DA neurons appropriate for cell therapy in PD.

Mesh Headings (Keywords): Animals, Biological Markers, Bone Morphogenetic Proteins, Carrier Proteins, Cells, Cultured, Dopamine, Embryonic Stem Cells, Female, Gene Expression Regulation, Humans, Mesencephalon, Neuroepithelial Cells, Neurons, Phenotype, RNA, Messenger, Rats, Rats, Sprague-Dawley, Stem Cell Transplantation


Check for Full Text / PubMed Unique Identifier (PMID): 17038668


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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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