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The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.
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How to make an oligodendrocyte.

Steven A Goldman1, Nicholas J Kuypers2

  • 1Center for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY 14642, USA Center for Basic and Translational Neuroscience, University of Copenhagen, Faculty of Health and Medical Sciences, Copenhagen 2200, Denmark Neuroscience Center, Rigshospitalet, Copenhagen 2100, Denmark steven_goldman@urmc.rochester.edu.

Development (Cambridge, England)
|December 3, 2015
PubMed
Summary
This summary is machine-generated.

Replacing lost oligodendrocytes offers therapeutic potential for central white matter diseases. This primer explores oligodendrocyte development, stem cell-derived progenitor production, and transplantation safety for myelin repair.

Keywords:
AstrocyteGlial progenitor cellLeukodystrophyMultiple sclerosisMyelinNeural stem cellRemyelinationStem cellWhite matter

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Area of Science:

  • Neuroscience
  • Cell Biology
  • Regenerative Medicine

Background:

  • Oligodendrocytes produce myelin, essential for axonal impulse conduction.
  • Oligodendrocyte loss causes demyelination, leading to neurological impairments in various diseases.
  • Replacing lost oligodendrocytes is a promising therapeutic strategy for central white matter disorders.

Purpose of the Study:

  • To describe molecular events in oligodendrocyte development.
  • To outline methods for producing oligodendrocyte progenitor cells (OPCs) from stem cells and somatic cells.
  • To discuss the safety and in vivo modulation of transplanted OPCs.

Main Methods:

  • Review of molecular mechanisms regulating oligodendrocyte development.
  • Description of stem cell (embryonic and induced pluripotent) and somatic cell differentiation protocols for OPC production.
  • Analysis of safety data and strategies for modulating engrafted OPC differentiation and myelinogenesis.

Main Results:

  • Detailed understanding of oligodendrocyte development pathways.
  • Established methods for generating OPCs from various cell sources.
  • Insights into the safety and therapeutic potential of stem cell-derived OPC transplantation.

Conclusions:

  • Oligodendrocyte replacement therapy holds significant promise for treating demyelinating diseases.
  • Advances in cell production and transplantation techniques are crucial for therapeutic success.
  • Further research on in vivo modulation will optimize myelin repair strategies.