Mutual effects of caveolin and nerve growth factor signaling in pig oligodendrocytes

J Neurosci Res. 2010 Feb 15;88(3):572-88. doi: 10.1002/jnr.22235.

Abstract

Signaling of growth factors may depend on the recruitment of their receptors to specialized microdomains. Previous reports on PC12 cells indicated an interaction of raft-organized caveolin and TrkA signaling. Because porcine oligodendrocytes (OLs) respond to nerve growth factor (NGF), we were interested to know whether caveolin also plays a role in oligodendroglial NGF/TrkA signaling. OLs expressed caveolin at the plasma membrane but also intracellularly. This was partially organized in the classically Omega-shaped invaginations, which may represent caveolae. We could show that caveolin and TrkA colocalize by using a discontinuous sucrose gradient (Song et al. [1996] J. Biol. Chem. 271:9690-9697), MACS technology, and immunoprecipitation. However, differential extraction of caveolin and TrkA with Triton X-100 at 4 degrees C indicated that caveolin and TrkA are probably not exclusively present in detergent-resistant, caveolin-containing rafts (CCRs). NGF treatment of OLs up-regulated the expression of caveolin-1 (cav-1) and stimulated tyrosine-14 phosphorylation of cav-1. Furthermore, OLs were transfected with cav-1-specific small interfering RNA (siRNA). A knockdown of cav-1 resulted in a reduced activation of downstream components of the NGF signaling cascade, such as p21Ras and mitogen-activated protein kinase (MAPK) after NGF exposure of OLs. Subsequently, increased oligodendroglial process formation via NGF was impaired. The present study indicates that CCRs/caveolin could play a modulating role during oligodendroglial differentiation and regeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / metabolism*
  • Caveolin 1 / genetics
  • Caveolin 1 / metabolism
  • Caveolins / genetics
  • Caveolins / metabolism*
  • Cell Membrane / metabolism
  • Cells, Cultured
  • Down-Regulation
  • Gene Knockdown Techniques
  • Intracellular Space / metabolism
  • Mitogen-Activated Protein Kinases / metabolism
  • Myelin Sheath / metabolism
  • Nerve Growth Factor / metabolism*
  • Oligodendroglia / metabolism*
  • Phosphorylation
  • Proto-Oncogene Proteins p21(ras) / metabolism
  • RNA, Small Interfering
  • Receptor, trkA / metabolism
  • Signal Transduction
  • Swine

Substances

  • Caveolin 1
  • Caveolins
  • RNA, Small Interfering
  • Nerve Growth Factor
  • Receptor, trkA
  • Mitogen-Activated Protein Kinases
  • Proto-Oncogene Proteins p21(ras)