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      Generation of Definitive Neural Progenitor Cells from Human Pluripotent Stem Cells for Transplantation into Spinal Cord Injury.

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          Abstract

          In this chapter, we first describe two interchangeable protocols optimized in our lab for deriving definitive neuronal progenitor cells from human pluripotent stem cells (hPSCs). The resultant NPCs can then be propagated and differentiated to produce differing proportions of neurons, oligodendrocytes, and astrocytes as required for in vitro cell culture studies or in vivo transplantation. Following these protocols, we explain the method for transplanting these cells into the rat model of spinal cord injury (SCI).

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          Author and article information

          Journal
          Methods Mol Biol
          Methods in molecular biology (Clifton, N.J.)
          Springer Science and Business Media LLC
          1940-6029
          1064-3745
          2019
          : 1919
          Affiliations
          [1 ] Division of Genetics and Development, Krembil Research Institute, Toronto, ON, Canada.
          [2 ] Institute of Medical Science, University of Toronto, Toronto, ON, Canada.
          [3 ] Division of Neurosurgery, University of Toronto, Toronto, ON, Canada.
          [4 ] Division of Genetics and Development, Krembil Research Institute, Toronto, ON, Canada. Michael.Fehlings@uhn.ca.
          [5 ] Institute of Medical Science, University of Toronto, Toronto, ON, Canada. Michael.Fehlings@uhn.ca.
          [6 ] Division of Neurosurgery, University of Toronto, Toronto, ON, Canada. Michael.Fehlings@uhn.ca.
          [7 ] Spinal Program, Toronto Western Hospital, University Health Network, Toronto, ON, Canada. Michael.Fehlings@uhn.ca.
          [8 ] Faculty of Medicine, University of Toronto, Toronto, ON, Canada. Michael.Fehlings@uhn.ca.
          Article
          10.1007/978-1-4939-9007-8_3
          30656619
          28f81b5f-e688-43d9-90e8-972d872a89b6
          History

          Pluripotent stem cells,Spinal cord injury,Neural progenitor cells,Cell transplantation

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