Neuronal progenitors identified by their inability to express class I histocompatibility antigens in response to interferon-gamma

J Neurosci Res. 1994 Oct 1;39(2):166-77. doi: 10.1002/jnr.490390207.

Abstract

Interferon-gamma (IFN-gamma) can induce class I major histocompatibility complex (MHC) antigen (H-2) expression on virtually all neuroepithelial cells isolated from embryonic day 9 (E9) mice. However, a subpopulation of cells become refractory to H-2 induction (H-21-) by E10 and the percentage of H-2 noninducible cells increases during development. Cell sorting, by flow cytometry or magnetic bead immunoselection, has shown that H-21- cells give rise exclusively to neuronal cells, and by E12, the majority of the neuronal progenitors are found within this population. It has also been found that 98% of the H-21- also express the neuron-associated marker, A2B5. Cells of the glial cell lineage retain the ability to express class I antigens throughout development. From these studies, it is clear that the neuroepithelium contains cells committed to the neuronal cell lineage as early as E10 in the mouse.

MeSH terms

  • Animals
  • Antigens, Surface / analysis
  • Cell Differentiation
  • Cell Separation
  • Cells, Cultured
  • Epithelial Cells
  • Epithelium / immunology
  • Flow Cytometry
  • Gene Expression Regulation, Developmental / drug effects*
  • Gestational Age
  • H-2 Antigens / biosynthesis*
  • H-2 Antigens / genetics
  • Immunomagnetic Separation
  • Interferon-gamma / pharmacology*
  • Mesencephalon / cytology
  • Mesencephalon / embryology
  • Mesencephalon / immunology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Nerve Tissue Proteins / biosynthesis*
  • Nerve Tissue Proteins / genetics
  • Neurons / cytology*
  • Recombinant Proteins
  • Stem Cells / drug effects*
  • Stem Cells / immunology
  • Stem Cells / metabolism
  • Telencephalon / cytology
  • Telencephalon / embryology
  • Telencephalon / immunology

Substances

  • Antigens, Surface
  • H-2 Antigens
  • Nerve Tissue Proteins
  • Recombinant Proteins
  • Interferon-gamma