Characterization and changes in neurotrophin receptor p75-Expressing motor neurons in SOD1(G93A) G1H mice [corrected]

J Comp Neurol. 2015 Aug 1;523(11):1664-82. doi: 10.1002/cne.23763. Epub 2015 Apr 30.

Abstract

Mice with high numbers of the Cu/Zn superoxide dismutase-1 G93A transgene (SOD1(G93A) G1H) have become the most commonly used animal model to study amyotrophic lateral sclerosis. This study investigated changes in size, numbers, and cell stress/death markers of motor neuron numbers in G1H mice that re-express the common p75 neurotrophin receptor (p75NTR). SOD1(G93A) G1H mice and age-matched C57BL/6J controls at 60, 80, 100, 120 days and end stage/140 days were analyzed for p75NTR, choline acetyltransferase (ChAT), activating transcription factor 3 (ATF3), and cleaved caspase-3. In addition, motor neuron counts and soma sizes were recorded. Motor neurons re-expressing p75NTR in SOD1(G93A) G1H mice were first observed at 80 days, and this continued to 140 days, peaking at 100-120 days at ∼5%. The soma area of motor neurons re-expressing p75NTR was always 600-800 µm(2) , suggesting that these are alpha motor neurons, which was confirmed after examination of somas post injection of a retrogradely transported antibody to p75NTR in 110-day-old SOD1(G93A) G1H mice. In motor neurons not re-expressing p75NTR, the frequency of small soma 200-400 µm2 motor neurons increased, whereas the larger 600-900 µm2 motor neurons decreased with progression, indicating that large motor neurons were dying off and shrinking in the process. There was minimal coexpression of p75NTR with ATF3, a marker for cell stress, but 85% coexpressed the apoptotic marker cleaved caspase-3. These findings indicate that in SOD1(G93A) G1H mice, p75NTR re-expression is detectable from 80 days in a small population of large motor neurons that represent 5% of the total motor neurons. Furthermore, p75NTR re-expression occurs in larger alpha motor neurons that express cleaved caspsase-3 and are destined to die.

Keywords: RRID: AB_1852703; RRID: AB_2258513; RRID: AB_2314091; RRID: AB_2314176; RRID: AB_791009; RRID: IMSR_JAX:000664; RRID: IMSR_JAX:002300; RRID: nif-0000-30467; RRID: rid_000042; RRID: rid_000081; SOD1G93A; amyotrophic lateral sclerosis; p75NTR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activating Transcription Factor 3 / metabolism
  • Aging / metabolism
  • Aging / pathology
  • Amyotrophic Lateral Sclerosis / metabolism*
  • Amyotrophic Lateral Sclerosis / pathology*
  • Animals
  • Caspase 3 / metabolism
  • Cell Count
  • Cell Size
  • Choline O-Acetyltransferase / metabolism
  • Disease Models, Animal
  • Disease Progression
  • Humans
  • Immunohistochemistry
  • Lumbar Vertebrae
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Motor Neurons / metabolism*
  • Motor Neurons / pathology*
  • Neurites / metabolism
  • Neurites / pathology
  • Receptors, Nerve Growth Factor / metabolism*
  • Spinal Cord / metabolism
  • Spinal Cord / pathology
  • Superoxide Dismutase / genetics

Substances

  • Activating Transcription Factor 3
  • Atf3 protein, mouse
  • Receptors, Nerve Growth Factor
  • Ngfr protein, mouse
  • SOD1 G93A protein
  • Superoxide Dismutase
  • Choline O-Acetyltransferase
  • Casp3 protein, mouse
  • Caspase 3