Multipotentiality, homing properties, and pyramidal neurogenesis of CNS-derived LeX(ssea-1)+/CXCR4+ stem cells

FASEB J. 2005 Nov;19(13):1860-2. doi: 10.1096/fj.05-4170fje. Epub 2005 Sep 8.

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

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism
  • Animals
  • Apoptosis
  • Bacterial Proteins / metabolism
  • Blotting, Western
  • Brain / embryology
  • Brain / metabolism
  • Cell Differentiation
  • Cell Lineage
  • Cell Movement
  • Cell Proliferation
  • Cell Separation
  • Cell Survival
  • Central Nervous System / metabolism*
  • Chemotaxis
  • Flow Cytometry
  • Green Fluorescent Proteins / metabolism
  • Hematopoietic Stem Cells / cytology
  • Hippocampus / metabolism
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization, Fluorescence
  • Lewis X Antigen / genetics
  • Luminescent Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Microscopy, Fluorescence
  • Models, Biological
  • Muscle, Skeletal / pathology
  • Neurodegenerative Diseases / metabolism
  • Neurodegenerative Diseases / therapy
  • Neurons / cytology*
  • Neurons / metabolism
  • Phenotype
  • Receptors, CXCR4 / biosynthesis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction
  • Stem Cell Transplantation / methods*
  • Stem Cells / cytology*
  • Time Factors
  • Transcription, Genetic

Substances

  • Actins
  • Bacterial Proteins
  • Lewis X Antigen
  • Luminescent Proteins
  • Receptors, CXCR4
  • yellow fluorescent protein, Bacteria
  • Green Fluorescent Proteins