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Differential fate of multipotent and lineage-restricted neural precursors following transplantation into the adult CNS
Journal article   Open access

Differential fate of multipotent and lineage-restricted neural precursors following transplantation into the adult CNS

ANGELO C. Lepore, STEVEN S.W. Han, CARLA J. TYLER-POLSZ, JINGLI Cai, MAHENDRA S. Rao and ITZHAK Fischer
Neuron glia biology, v 1(2), pp 113-126
01 May 2004
PMID: 16520830
url
https://europepmc.org/articles/pmc1389711View
Accepted (AM)Open Access (License Unspecified) Open

Abstract

glial cells neural progenitors neurons spinal cord injury Stem cells
Multiple classes of precursor cells have been isolated and characterized from the developing spinal cord including multipotent neuroepithelial (NEP) stem cells and lineage-restricted precursors for neurons (NRPs) and glia (GRPs). We have compared the survival, differentiation and integration of multipotent NEP cells with lineage-restricted NRPs and GRPs using cells isolated from transgenic rats that express the human placental alkaline phosphatase gene. Our results demonstrate that grafted NEP cells survive poorly, with no cells observed 3 days after transplant in the adult hippocampus, striatum and spinal cord, indicating that most CNS regions are not compatible with transplants of multipotent cells derived from fetal CNS. By contrast, at 3 weeks and 5 weeks post-engraftment, lineage-restricted precursors showed selective migration along white-matter tracts and robust survival in all three CNS regions. The grafted precursors expressed the mature neuronal markers NeuN and MAP2, the astrocytic marker GFAP, the oligodendrocytic markers RIP, NG2 and Sox-10, and the synaptic marker synaptophysin. Similar behavior was observed when these precursors were transplanted into the injured spinal cord. Predifferentiated, multipotent NEP cells also survive and integrate, which indicates that lineage-restricted CNS precursors are well suited for transplantation into the adult CNS and provide a promising cellular replacement candidate.

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Collaboration types
Domestic collaboration
Web of Science research areas
Neurosciences
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