Spinal cord-specific deletion of the glutamate transporter GLT1 causes motor neuron death in mice

Biochem Biophys Res Commun. 2018 Mar 4;497(2):689-693. doi: 10.1016/j.bbrc.2018.02.132. Epub 2018 Feb 16.

Abstract

Amyotrophic lateral sclerosis (ALS) is a chronic neurodegenerative disorder characterized by the selective loss of motor neurons. The precise mechanisms that cause the selective death of motor neurons remain unclear, but a growing body of evidence suggests that glutamate-mediated excitotoxicity has been considered to play an important role in the mechanisms of motor neuron degeneration in ALS. Reductions in glutamate transporter GLT1 have been reported in animal models of ALS and the motor cortex and spinal cord of ALS patients. However, it remains unknown whether the reduction in GLT1 has a primary role in the induction of motor neuron degeneration in ALS. Here, we generated conditional knockout mice that lacked GLT1 specifically in the spinal cord by crossing floxed-GLT1 mice and Hoxb8-Cre mice. Hoxb8-Cre/GLT1flox/flox mice showed motor deficits and motor neuron loss. Thus, loss of the glial glutamate transporter GLT1 is sufficient to cause motor neuron death in mice.

Keywords: Amyotrophic lateral sclerosis; Excitotoxicity; GLT1; Glutamate transporter; Motor neuron.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyotrophic Lateral Sclerosis / genetics*
  • Amyotrophic Lateral Sclerosis / pathology
  • Animals
  • Cell Death
  • Excitatory Amino Acid Transporter 2 / genetics*
  • Gene Deletion*
  • Gliosis / genetics*
  • Gliosis / pathology
  • Male
  • Mice
  • Mice, Knockout
  • Motor Neurons / metabolism
  • Motor Neurons / pathology*
  • Spinal Cord / metabolism
  • Spinal Cord / pathology*

Substances

  • Excitatory Amino Acid Transporter 2
  • Slc1a2 protein, mouse