Identification of novel spinal cholinergic genetic subtypes disclose Chodl and Pitx2 as markers for fast motor neurons and partition cells

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Anders Enjin - , Uppsala University (Author)
  • Nadine Rabe - , Department of Psychiatry and Psychotherapy, Uppsala University (Author)
  • Stan T Nakanishi - (Author)
  • Anna Vallstedt - (Author)
  • Henrik Gezelius - (Author)
  • Fatima Memic - (Author)
  • Magnus Lind - (Author)
  • Tord Hjalt - (Author)
  • Warren G Tourtellotte - (Author)
  • Carl Bruder - (Author)
  • Gregor Eichele - (Author)
  • Patrick J Whelan - (Author)
  • Klas Kullander - (Author)

Abstract

Spinal cholinergic neurons are critical for motor function in both the autonomic and somatic nervous systems and are affected in spinal cord injury and in diseases such as amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy. Using two screening approaches and in situ hybridization, we identified 159 genes expressed in typical cholinergic patterns in the spinal cord. These include two general cholinergic neuron markers, one gene exclusively expressed in motor neurons, and nine genes expressed in unknown subtypes of somatic motor neurons. Further, we present evidence that chondrolectin (Chodl) is expressed by fast motor neurons and that estrogen-related receptor beta (ERRbeta) is a candidate marker for slow motor neurons. In addition, we suggest paired-like homeodomain transcription factor 2 (Pitx2) as a marker for cholinergic partition cells.

Details

Original languageEnglish
Pages (from-to)2284-304
Number of pages21
JournalThe Journal of comparative neurology
Volume518
Issue number12
Publication statusPublished - 15 Jun 2010
Peer-reviewedYes

External IDs

Scopus 77952150453
ORCID /0000-0002-3188-8431/work/142251773

Keywords

Keywords

  • Animals, Fluorescent Antibody Technique, Homeodomain Proteins/genetics, In Situ Hybridization, Lectins, C-Type/genetics, Mice, Mice, Inbred C57BL, Motor Neurons/cytology, Oligonucleotide Array Sequence Analysis, Patch-Clamp Techniques, Receptors, Estrogen/genetics, Spinal Cord/cytology, Transcription Factors/genetics