Enhanced expression of 14-3-3 family members in injured motoneurons

Brain Res Mol Brain Res. 1998 Apr;55(2):315-20. doi: 10.1016/s0169-328x(98)00012-6.

Abstract

An increase in 14-3-3 mRNA expression after hypoglossal nerve injury was demonstrated by RNA finger printing using the arbitrary primed polymerase chain reaction (RAP-PCR). RAP-PCR was carried out to compare differences in mRNA expression between axotomized (6 h after the transection) and normal hypoglossal nuclei in mice. The expression of several gene fragments was increased after nerve injury; one fragment was identified as 14-3-3 which is an activator of Raf-1. Since a family of 14-3-3 genes are identified in the rat, we examined the expression of five members of the rat 14-3-3 family after injury (beta, gamma, zeta, eta and theta). Among these family members, a substantial up-regulation in mRNA expression was observed for the zeta and θ forms. Subsequent emulsion autoradiography of hybridization tissue sections revealed an increase in zeta and theta mRNA in injured motoneurons. Since 14-3-3 has the ability to dimerize and activate Raf-1, the up-regulation of 14-3-3 expression would be expected to facilitate the Ras-Erk signal pathway by Raf-1 activation. Our previous results have demonstrated that Shc, Erk1 and Mek1 mRNAs are up-regulated during nerve regeneration, whereas PKA which inhibits the Ras-Erk pathway via Raf-1 was down-regulated. Taken together, the present results suggest that enhancement in expression of molecules involved in the Ras-Erk signaling is required for peripheral nerve regeneration.

Publication types

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

MeSH terms

  • 14-3-3 Proteins
  • Animals
  • Axotomy
  • Hypoglossal Nerve / physiology
  • In Situ Hybridization
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Motor Neurons / metabolism*
  • Multigene Family
  • Primed In Situ Labeling
  • Protein Biosynthesis*
  • Proteins / genetics
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Wistar
  • Sequence Analysis, DNA
  • Tyrosine 3-Monooxygenase*

Substances

  • 14-3-3 Proteins
  • Proteins
  • RNA, Messenger
  • Tyrosine 3-Monooxygenase