DEVELOPMENT OF THE SYNAPSE

Information

  • Research Project
  • 6393389
  • ApplicationId
    6393389
  • Core Project Number
    R01NS023583
  • Full Project Number
    7R01NS023583-16
  • Serial Number
    23583
  • FOA Number
  • Sub Project Id
  • Project Start Date
    4/1/1986 - 38 years ago
  • Project End Date
    6/30/2003 - 21 years ago
  • Program Officer Name
    NICHOLS, PAUL L
  • Budget Start Date
    8/1/2001 - 23 years ago
  • Budget End Date
    6/30/2002 - 22 years ago
  • Fiscal Year
    2001
  • Support Year
    16
  • Suffix
  • Award Notice Date
    9/18/2001 - 23 years ago

DEVELOPMENT OF THE SYNAPSE

DESCRIPTION (Adapted from the applicant's abstract): At vertebrate neuromuscular junctions, the transmission of signal from the nerve to the muscle which causes muscle contraction is mediated by the release of acetylcholine from the nerve terminal and the sensing of this molecule by the receptors in the muscle. This is accomplished by the clustering of acetylcholine receptors in the postsynaptic membrane opposite to the nerve terminal and the focal accumulation of synaptic vesicles, which contain acetylcholine in the nerve terminal. The objective of this study is to understand the development of this prototypical synapse. In particular, the investigator seeks to unravel cellular and molecular mechanisms that govern the development of the postsynaptic membrane of the neuromuscular junction. The specific aims are: (1) to understand the interplay between agrin, heparin-binding growth factors and receptor tyrosine kinases in the signaling of the postsynaptic development; (2) to examine the role of the postsynaptic actin-based cytoskeleton in serving as a scaffolding for the assembly and the stabilization of postsynaptic specializations; and (3) to study the mechanism for the clustering of acetylcholinesterase in the postsynaptic membrane and the cellular machinery for generating the transmembrane macromolecular complex at the neuromuscular junction. Tissue cultures of spinal cord neurons and muscle cells from amphibian embryos will be used as the model system in this study. A range of techniques, including microscopy, immunocytochemistry, protein biochemistry, molecular biology and electrophysiology, will be used to observe the development of the neuromuscular junction in tissue culture. These studies should lead to advancement in our understanding of the biogenesis of this peripheral synapse. The principles garnered from this study should also be useful in understanding synaptic development in the central nervous system. Many neurological and neuromuscular disorders are results of malfunctions of synaptic connections in the nervous system. The fundamental knowledge on the motor innervation of the muscle obtained from this study should also lead to a better understanding of the causes of these maladies.

IC Name
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
  • Activity
    R01
  • Administering IC
    NS
  • Application Type
    7
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    192186
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    853
  • Ed Inst. Type
  • Funding ICs
    NINDS:192186\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    HONG KONG UNIV OF SCIENCE &TECHNOLOGY
  • Organization Department
  • Organization DUNS
  • Organization City
    KOWLOON
  • Organization State
  • Organization Country
    HONG KONG
  • Organization Zip Code
  • Organization District
    HONG KONG