Alsin/Rac1 signaling controls survival and growth of spinal motoneurons

Ann Neurol. 2006 Jul;60(1):105-17. doi: 10.1002/ana.20886.

Abstract

Objective: Recessive mutations in alsin, a guanine-nucleotide exchange factor for the GTPases Rab5 and Rac1, cause juvenile amyotrophic lateral sclerosis (ALS2) and related motoneuron disorders. Alsin function in motoneurons remained unclear because alsin knock-out mice do not develop overt signs of motoneuron degeneration.

Methods: To generate an alsin loss-of-function model in an ALS-relevant cell type, we developed a new small interfering RNA electroporation technique that allows efficient knock down of alsin in embryonic rat spinal motoneurons.

Results: After small interfering RNA-mediated alsin knockdown, cultured motoneurons displayed a reduced apparent size of EEA1-labeled early endosomes and an increased intracellular accumulation of transferrin and L1CAM. Alsin knockdown induced cell death in 32 to 48% of motoneurons and significantly inhibited axon growth in the surviving neurons. Both cellular phenotypes were mimicked by expression of a dominant-negative Rac1 mutant and were completely blocked by expression of a constitutively active Rac1 mutant. Expression of dominant-negative or constitutively active forms of Rab5 had no such effects.

Interpretation: Our data demonstrate that alsin controls the growth and survival of motoneurons in a Rac1-dependant manner. The strategy reported here illustrates how small interfering RNA electroporation can be used to generate cellular models of neurodegenerative disease involving a loss-of-function mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axons / physiology
  • COS Cells
  • Cell Death / physiology
  • Cell Division / physiology
  • Cell Survival / physiology
  • Chlorocebus aethiops
  • Electroporation / methods
  • Endosomes / metabolism
  • Guanine Nucleotide Exchange Factors / genetics
  • Guanine Nucleotide Exchange Factors / metabolism*
  • Motor Neurons / cytology*
  • Motor Neurons / metabolism
  • Motor Neurons / ultrastructure
  • Neuropeptides / genetics
  • Neuropeptides / metabolism*
  • Phenotype
  • RNA, Small Interfering / pharmacokinetics
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / physiology*
  • Spinal Cord / cytology*
  • rac GTP-Binding Proteins / genetics
  • rac GTP-Binding Proteins / metabolism*
  • rac1 GTP-Binding Protein

Substances

  • Als2 protein, mouse
  • Guanine Nucleotide Exchange Factors
  • Neuropeptides
  • RNA, Small Interfering
  • Rac1 protein, mouse
  • rac GTP-Binding Proteins
  • rac1 GTP-Binding Protein