髓鞘
神经干细胞
轴突
细胞生物学
神经突
生物
诱导多能干细胞
干细胞
神经科学
中枢神经系统
生物化学
体外
胚胎干细胞
基因
作者
Gunnar Poplawski,Richard Lie,Matthew A. Hunt,Hiromi Kumamaru,Riki Kawaguchi,Paul Lu,Michael K. E. Schäfer,Grace Woodruff,Jacob Robinson,Philip Canete,Jennifer N. Dulin,Cédric G. Geoffroy,Lutz Menzel,Binhai Zheng,Giovanni Coppola,Mark H. Tuszynski
出处
期刊:Science Translational Medicine
[American Association for the Advancement of Science (AAAS)]
日期:2018-05-23
卷期号:10 (442)
被引量:33
标识
DOI:10.1126/scitranslmed.aal2563
摘要
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.
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