Abstract
Achieving efficient distribution of neural stem cells throughout the central nervous system (CNS) and robust generation of specific neurons is a major challenge for the development of cell-mediated therapy for neurodegenerative diseases. We isolated a primitive neural stem cell subset, double positive for LeX(Le) and CXCR4(CX) antigens that possesses CNS homing potential and extensive neuronal repopulating capacity. Le+CX+ cells are multipotential and can generate neurons as well as myogenic and endothelial cells. In vivo Le+CX+ cells displayed widespread incorporation and differentiated into cortical and hippocampal pyramidal neurons. Since intravenous delivery could be a less invasive route of transplantation, we investigated whether Le+CX+ cells could migrate across endothelial monolayers. Intracerebral coadministration of SDF enabled migration of intravenously injected Le+CX+ cells into the CNS and a small, yet significant, number of donor cells differentiated into neurons. The isolation of a specific neural stem cell population could offer major advantages to neuronal replacement strategies.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Actins / metabolism
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Animals
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Apoptosis
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Bacterial Proteins / metabolism
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Blotting, Western
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Brain / embryology
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Brain / metabolism
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Cell Differentiation
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Cell Lineage
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Cell Movement
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Cell Proliferation
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Cell Separation
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Cell Survival
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Central Nervous System / metabolism*
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Chemotaxis
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Flow Cytometry
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Green Fluorescent Proteins / metabolism
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Hematopoietic Stem Cells / cytology
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Hippocampus / metabolism
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Humans
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Immunohistochemistry
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In Situ Hybridization, Fluorescence
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Lewis X Antigen / genetics
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Luminescent Proteins / metabolism
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Mice
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Mice, Inbred C57BL
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Microscopy, Fluorescence
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Models, Biological
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Muscle, Skeletal / pathology
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Neurodegenerative Diseases / metabolism
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Neurodegenerative Diseases / therapy
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Neurons / cytology*
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Neurons / metabolism
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Phenotype
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Receptors, CXCR4 / biosynthesis
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Reverse Transcriptase Polymerase Chain Reaction
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Signal Transduction
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Stem Cell Transplantation / methods*
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Stem Cells / cytology*
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Time Factors
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Transcription, Genetic
Substances
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Actins
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Bacterial Proteins
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Lewis X Antigen
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Luminescent Proteins
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Receptors, CXCR4
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yellow fluorescent protein, Bacteria
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Green Fluorescent Proteins