Morphological phenotypes of olfactory ensheathing cells display different migratory responses upon Slit-2

Exp Cell Res. 2012 Sep 10;318(15):1889-900. doi: 10.1016/j.yexcr.2012.05.024. Epub 2012 Jun 5.

Abstract

Olfactory ensheathing cells (OECs) are a type of glial cells with morphological plasticity in the olfactory system. Cultured OECs display the process-bearing and flattened shape. Our previous studies have shown that the frontal application of Slit-2 gradient induced the collapse of leading front, and reversed the soma translocation of process-bearing OECs. However, the migratory properties of flattened OECs upon Slit-2 gradient remain elusive. Here, we found that Slit-2 gradient induced the collapse of their plasma membrane, and inhibited migration of flattened OECs. Upon to Slit-2 gradient, the leading front of flattened type 1 OECs firstly showed collapse and retraction, then gradually re-grew a new lamellipodia, finally, showed collapse again (this phenomenon was called as adaptation), while flattened type 2 OECs only showed collapse of plasma membrane. These different migratory responses upon Slit-2 stimulation were possibly due to their different sub-cellular distribution of Robo receptor. Furthermore, F-actin at the peripheral region of leading front was more sensitive to the Slit-2 stimulation than microtubules and the loss of F-actin might be implicated in initiating the collapse of flattened OECs. Finally, the adaptation of flattened type 1 OECs induced by Slit-2 was independent on protein synthesis. Taken together, these results demonstrate that morphological phenotypes of OECs display different migratory properties upon Slit-2 and an unexpected finding that the protein synthesis-independent adaptation in OECs induced by Slit-2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Movement / drug effects
  • Cell Movement / physiology
  • Cell Polarity
  • Cell Shape / drug effects
  • Cell Shape / physiology
  • Cells, Cultured
  • Cycloheximide / pharmacology
  • Intercellular Signaling Peptides and Proteins / pharmacology*
  • Intercellular Signaling Peptides and Proteins / physiology*
  • Nerve Tissue Proteins / pharmacology*
  • Nerve Tissue Proteins / physiology*
  • Neuroglia / cytology
  • Neuroglia / drug effects*
  • Neuroglia / physiology*
  • Olfactory Pathways / cytology*
  • Olfactory Pathways / drug effects*
  • Olfactory Pathways / physiology
  • Protein Synthesis Inhibitors / pharmacology
  • Rats
  • Receptors, Immunologic / genetics
  • Receptors, Immunologic / metabolism
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Recombinant Proteins / pharmacology
  • Subcellular Fractions / metabolism

Substances

  • Intercellular Signaling Peptides and Proteins
  • Nerve Tissue Proteins
  • Protein Synthesis Inhibitors
  • Receptors, Immunologic
  • Recombinant Proteins
  • Robo2 protein, rat
  • Cycloheximide
  • Slit homolog 2 protein