Sphere formation of ocular epithelial cells in the ciliary body is a reprogramming system for neural differentiation

Brain Res. 2006 Jun 6;1093(1):54-70. doi: 10.1016/j.brainres.2006.03.093. Epub 2006 May 11.

Abstract

It is well known that neural stem/progenitor cells of the central nervous system (CNS) can proliferate to form neurospheres (CNS-neurospheres) that are positive for nestin, an intermediate filament for neural progenitors. Retinal stem/progenitor properties were also isolated from the ciliary body (CB) of the eye where, as in the CNS, such stem/progenitors also form spheres and have been considered to expand only via expansion by their proliferation even from the single-cell level (called spheres of pigment cells from the ciliary margin: PCM-spheres). We here found a new and distinct process underlying the growth of CB cell-derived spheres (CB-spheres) that is unlike the mechanism of CNS- and PCM-sphere expansion; this new process is a cell proliferation-independent incorporation of neighbor spheres and cells cultured at high density (200 cells/mul). The majority of cells in CB-spheres consisted of nestin-negative epithelia-like cells and started to express nestin during the course of their expansion by high-density cultivation. The growth of CNS-neurospheres was sensitive to a cell-cycle inhibitor, whereas the growth of CB-spheres was not seriously affected by cell proliferation; rather, the spheres grew by incorporating other CB-spheres and nestin-negative adherent cells, the latter of which started to express nestin and lost the expression of epithelial markers after being incorporated. These results indicate that CB-spheres do not form by the accumulation of neural progenitors but rather by a reprogramming system from epithelia-like cells for neural differentiation, a clearly distinct mechanism from sphere formation by single-cell expansion of retinal stem/progenitor populations.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aphidicolin / pharmacology
  • Cell Adhesion / physiology
  • Cell Culture Techniques
  • Cell Differentiation / physiology*
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Ciliary Body / cytology*
  • Ciliary Body / metabolism
  • Ciliary Body / ultrastructure
  • Enzyme Inhibitors / pharmacology
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism
  • Epithelial Cells / ultrastructure
  • Flow Cytometry
  • Immunohistochemistry
  • Intermediate Filament Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microscopy, Electron, Transmission
  • Nerve Tissue Proteins / metabolism
  • Nestin
  • Neurons / cytology*
  • Neurons / metabolism
  • Neurons / ultrastructure
  • Stem Cells / cytology*
  • Stem Cells / metabolism
  • Stem Cells / ultrastructure

Substances

  • Enzyme Inhibitors
  • Intermediate Filament Proteins
  • Nerve Tissue Proteins
  • Nes protein, mouse
  • Nestin
  • Aphidicolin