Molecular mechanisms regulating motor neuron development and degeneration
- Author(s)
- Kilpatrick, TJ; Soilu-Hanninen, M;
- Details
- Publication Year 1999-06,Volume 19,Issue #3,Page 205-228
- Journal Title
- MOLECULAR NEUROBIOLOGY
- Publication Type
- Journal Article
- Abstract
- Motor neurons are a well-defined, although heterogeneous group of cells responsible for transmitting information from the central nervous system to the locomotor system. Spinal motor neurons are specified by soluble factors produced by structures adjacent to the primordial spinal cord, signaling through homeodomain proteins. Axonal pathfinding is regulated by cell-surface receptors that interact with extracellular ligands and once synaptic connections have formed, the survival of the somatic motor neuron is dependent on the provision of target-derived growth factors, although nontarget-derived factors, produced by either astrocytes or Schwann cells, are also potentially implicated. Somatic motor neuron degeneration leads to profound disability, and multiple pathogenetic mechanisms including aberrant growth factor signaling, abnormal neurofilament accumulation, excitotoxicity, and autoimmunity have been postulated to be responsible. Even when specific deficits have been identified, for example, mutations of the superoxide dismutase-l gene in familial amyotrophic sclerosis and polyglutamine expansion of the androgen receptor in spinal and bulbar muscular atrophy, the mechanisms by which somatic motor neuronal degeneration occurs remain unclear. In order to treat motor system degeneration effectively, we will need to understand these mechanisms more thoroughly.
- Publisher
- HUMANA PRESS INC
- Keywords
- AMYOTROPHIC-LATERAL-SCLEROSIS; NERVE GROWTH-FACTOR; CILIARY NEUROTROPHIC FACTOR; LEUKEMIA INHIBITORY FACTOR; SPINAL MUSCULAR-ATROPHY; INDUCED CELL-DEATH; RECEPTOR TYROSINE KINASE; CU,ZN SUPEROXIDE-DISMUTASE; AFFINITY NGF RECEPTOR; DISEASE GENE-PRODUCT
- Publisher's Version
- https://doi.org/10.1007/BF02821714
- Terms of Use/Rights Notice
- Refer to copyright notice on published article.
Creation Date: 1999-06-01 12:00:00