AI Article Synopsis

  • Oligodendrocytes are crucial for myelination in the central nervous system and play significant roles in neurodegenerative diseases.
  • The protocol outlines a fast and reliable method to differentiate human oligodendrocytes from pluripotent stem cells (PSCs) within 75 days, detailing key cell marker transitions throughout the differentiation process.
  • An alternative, cost-effective approach reduces differentiation time to around 55 days, achieving approximately 30% oligodendrocyte progenitor cells (O4(+)) more quickly.

Article Abstract

In the CNS, oligodendrocytes act as the myelinating cells. Oligodendrocytes have been identified to be key players in several neurodegenerative disorders. This protocol describes a robust, fast and reproducible differentiation protocol to generate human oligodendrocytes from pluripotent stem cells (PSCs) using a chemically defined, growth factor-rich medium. Within 8 d, PSCs differentiate into paired box 6-positive (PAX6(+)) neural stem cells, which give rise to OLIG2(+) progenitors by day 12. Oligodendrocyte lineage transcription factor 2-positive (OLIG2(+)) cells begin to express the transcription factor NKX2.2 around day 18, followed by SRY-box 10 (SOX10) around day 40. Oligodendrocyte progenitor cells (OPCs) that are positive for the cell surface antigen recognized by the O4 antibody (O4(+)) appear around day 50 and reach, on average, 43% of the cell population after 75 d of differentiation. O4(+) OPCs can be isolated by cell sorting for myelination studies, or they can be terminally differentiated to myelin basic protein-positive (MBP(+)) oligodendrocytes. This protocol also describes an alternative strategy for markedly reducing the length and the costs of the differentiation and generating ∼30% O4(+) cells after only 55 d of culture.

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Source
http://dx.doi.org/10.1038/nprot.2015.075DOI Listing

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