The receptor tyrosine kinase, Cek8, is transiently expressed on subtypes of motoneurons in the spinal cord during development

Mech Dev. 1996 Jan;54(1):59-69. doi: 10.1016/0925-4773(95)00461-0.

Abstract

Receptor tyrosine kinases (RTKs) play important roles in cellular proliferation, differentiation, and survival. We performed reverse transcriptase-polymerase chain reactions (RT-PCR) from enriched embryonic day 5 (E5) chick motoneurons by panning to identify RTKs involved in the early development of motoneuron. In situ hybridization revealed that Cek8, a member of the eph family, was specifically expressed on motoneurons at the brachial and lumbar segments of the spinal cord which innervate limb muscles, and disappeared after the naturally occurring cell death period (E6-E11). Immunohistochemistry using an anti-Cek8 monoclonal antibody showed the localization of Cek8 protein at the cell bodies and axonal fibers of motoneurons and muscles. The unique expression of Cek8 suggests its involvement in cellular survival or cell-cell interactions for specific subpopulations of developing motoneurons.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antibodies, Monoclonal / immunology
  • Apoptosis
  • Base Sequence
  • Cell Line
  • Cell Line, Transformed
  • Chick Embryo
  • Chlorocebus aethiops
  • Cloning, Molecular
  • DNA, Complementary / genetics
  • Enzyme Induction
  • Extremities / embryology
  • Extremities / innervation
  • Gene Expression Regulation, Developmental*
  • Humans
  • In Situ Hybridization
  • Kidney
  • Molecular Sequence Data
  • Motor Neurons / enzymology*
  • Nerve Tissue Proteins / biosynthesis*
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / immunology
  • Nerve Tissue Proteins / physiology
  • Neuromuscular Junction / enzymology
  • Neuropeptides / biosynthesis*
  • Neuropeptides / genetics
  • Neuropeptides / immunology
  • Neuropeptides / physiology
  • Polymerase Chain Reaction
  • Receptor Protein-Tyrosine Kinases / biosynthesis*
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptor Protein-Tyrosine Kinases / immunology
  • Receptor Protein-Tyrosine Kinases / physiology
  • Receptor, EphA4
  • Sequence Alignment
  • Spinal Cord / cytology
  • Spinal Cord / embryology*
  • Spinal Cord / enzymology
  • Transfection

Substances

  • Antibodies, Monoclonal
  • DNA, Complementary
  • Nerve Tissue Proteins
  • Neuropeptides
  • Receptor Protein-Tyrosine Kinases
  • Receptor, EphA4

Associated data

  • GENBANK/D38174