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The Stem Cell Factor Sox2 Is a Positive Timer of Oligodendrocyte Development in the Postnatal Murine Spinal Cord
Authors:Sheng Zhang  Abeer Rasai  Yan Wang  Jie Xu  Peter Bannerman  Daffcar Erol  Danayit Tsegaye  Aijun Wang  Athena Soulika  Xiangjiang Zhan  Fuzheng Guo
Institution:1.Institute for Pediatric Regenerative Medicine,Shriners Hospitals for Children/UC Davis School of Medicine,Sacramento,USA;2.Department of Neurology, School of Medicine,UC Davis,Davis,USA;3.Department of Cell Biology and Human Anatomy, School of Medicine,UC Davis,Davis,USA;4.Department of Surgery, School of Medicine,UC Davis,Davis,USA;5.Department of Dermatology, School of Medicine,UC Davis,Davis,USA;6.Key Laboratory of Animal Ecology and Conservation Biology, Institute of Zoology,Chinese Academy of Sciences,Beijing,China;7.Department of Neurology, UC Davis School of Medicine,c/o Shriners Hospitals for Children,Sacramento,USA
Abstract:Myelination in the central nervous system takes place predominantly during the postnatal development of humans and rodents by myelinating oligodendrocytes (OLs), which are differentiated from oligodendrocyte progenitor cells (OPCs). We recently reported that Sox2 is essential for developmental myelination in the murine brain and spinal cord. It is still controversial regarding the role of Sox2 in oligodendroglial lineage progression in the postnatal murine spinal cord. Analyses of a series of cell- and stage-specific Sox2 mutants reveal that Sox2 plays a biphasic role in regulating oligodendroglial lineage progression in the postnatal murine spinal cord. Sox2 controls the number of OPCs for subsequent differentiation through regulating their proliferation. In addition, Sox2 regulates the timing of OL differentiation and modulates the rate of oligodendrogenesis. Our experimental data prove that Sox2 is an intrinsic positive timer of oligodendroglial lineage progression and suggest that interventions affecting oligodendroglial Sox2 expression may be therapeutic for overcoming OPC differentiation arrest in dysmyelinating and demyelinating disorders.
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