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Disruption of the neurotrophin-3 receptor gene trkC eliminates la muscle afferents and results in abnormal movements

doi: 10.1038/368249a0
pmid: 8145824
Disruption of the neurotrophin-3 receptor gene trkC eliminates la muscle afferents and results in abnormal movements
The trkC gene is expressed throughout the mammalian nervous system and encodes a series of tyrosine protein kinase isoforms that serve as receptors for neurotrophin-3 (NT3), a member of the nerve growth factor (NGF) family of neurotrophic factors. One of these isoforms, gp145trkC/TrkC K1, mediates the trophic properties of NT3 in cultured cells. Here we show that homozygous mice defective for TrkC tyrosine protein kinase receptors lack Ia muscle afferent projections to spinal motor neurons and have fewer large myelinated axons in the dorsal root and posterior columns of the spinal cord. These mice display abnormal movements and postures, indicating that NT3/TrkC-dependent sensor; neurons may play a primary role in proprioception, the sense of position and movement of the limbs.
- University of Mary United States
- Washington State University United States
- Bristol-Myers Squibb (Germany) Germany
- European Molecular Biology Laboratory Germany
Heterozygote, Movement Disorders, Base Sequence, Muscles, RNA Splicing, Homozygote, Molecular Sequence Data, Posture, Receptor Protein-Tyrosine Kinases, Cell Count, DNA, Proprioception, Clone Cells, Mice, Inbred C57BL, Mice, Ganglia, Spinal, Mutation, Animals, Amino Acid Sequence, Neurons, Afferent
Heterozygote, Movement Disorders, Base Sequence, Muscles, RNA Splicing, Homozygote, Molecular Sequence Data, Posture, Receptor Protein-Tyrosine Kinases, Cell Count, DNA, Proprioception, Clone Cells, Mice, Inbred C57BL, Mice, Ganglia, Spinal, Mutation, Animals, Amino Acid Sequence, Neurons, Afferent
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