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Stem Cells Transl Med. 2018 Nov;7(11):806-818. doi: 10.1002/sctm.17-0269. Epub 2018 Aug 7.

Human Spinal Oligodendrogenic Neural Progenitor Cells Promote Functional Recovery After Spinal Cord Injury by Axonal Remyelination and Tissue Sparing.

Author information

1
Division of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
2
Department of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
3
New World Laboratories, Laval, Quebec, Canada.
4
Institute of Medical Sciences, University of Toronto, Toronto, Ontario, Canada.
5
Department of Surgery and Spine Program, University of Toronto, Toronto, Ontario, Canada.
6
Electron Microscope Laboratory, Keio University School of Medicine, Tokyo, Japan.

Abstract

Cell transplantation therapy utilizing neural precursor cells (NPCs) is a conceptually attractive strategy for traumatic spinal cord injury (SCI) to replace lost cells, remyelinate denuded host axons and promote tissue sparing. However, the number of mature oligodendrocytes that differentiate from typical NPCs remains limited. Herein, we describe a novel approach to bias the differentiation of directly reprogrammed human NPCs (drNPCs) toward a more oligodendrogenic fate (oNPCs) while preserving their tripotency. The oNPCs derived from different lines of human NPCs showed similar characteristics in vitro. To assess the in vivo efficacy of this approach, we used oNPCs derived from drNPCs and transplanted them into a SCI model in immunodeficient Rowett Nude (RNU) rats. The transplanted cells showed significant migration along the rostrocaudal axis and proportionally greater differentiation into oligodendrocytes. These cells promoted perilesional tissue sparing and axonal remyelination, which resulted in recovery of motor function. Moreover, after transplantation of the oNPCs into intact spinal cords of immunodeficient NOD/SCID mice, we detected no evidence of tumor formation even after 5 months of observation. Thus, biasing drNPC differentiation along an oligodendroglial lineage represents a promising approach to promote tissue sparing, axonal remyelination, and neural repair after traumatic SCI. Stem Cells Translational Medicine 2018;7:806-818.

KEYWORDS:

Oligodendrocytes; Oligodendrogenic neural progenitor cells; Regeneration; Remyelination; Spinal cord injury; Stem cells

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