| Literature DB >> 29794059 |
Gunnar H D Poplawski1, Richard Lie1, Matt Hunt1, Hiromi Kumamaru1, Riki Kawaguchi2, Paul Lu1,3, Michael K E Schäfer4, Grace Woodruff5, Jacob Robinson1, Philip Canete1, Jennifer N Dulin1, Cedric G Geoffroy1, Lutz Menzel4, Binhai Zheng1, Giovanni Coppola2, Mark H Tuszynski6,3.
Abstract
Axon regeneration after spinal cord injury (SCI) is attenuated by growth inhibitory molecules associated with myelin. We report that rat myelin stimulated the growth of axons emerging from rat neural progenitor cells (NPCs) transplanted into sites of SCI in adult rat recipients. When plated on a myelin substrate, neurite outgrowth from rat NPCs and from human induced pluripotent stem cell (iPSC)-derived neural stem cells (NSCs) was enhanced threefold. In vivo, rat NPCs and human iPSC-derived NSCs extended greater numbers of axons through adult central nervous system white matter than through gray matter and preferentially associated with rat host myelin. Mechanistic investigations excluded Nogo receptor signaling as a mediator of stem cell-derived axon growth in response to myelin. Transcriptomic screens of rodent NPCs identified the cell adhesion molecule neuronal growth regulator 1 (Negr1) as one mediator of permissive axon-myelin interactions. The stimulatory effect of myelin-associated proteins on rodent NPCs was developmentally regulated and involved direct activation of the extracellular signal-regulated kinase (ERK). The stimulatory effects of myelin on NPC/NSC axon outgrowth should be investigated further and could potentially be exploited for neural repair after SCI.Entities:
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Year: 2018 PMID: 29794059 DOI: 10.1126/scitranslmed.aal2563
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956