A versatile reporter for visualization of myelin plasticity in the genetically modified rat

Information

  • Research Project
  • 10303241
  • ApplicationId
    10303241
  • Core Project Number
    R21NS117983
  • Full Project Number
    1R21NS117983-01A1
  • Serial Number
    117983
  • FOA Number
    PA-18-358
  • Sub Project Id
  • Project Start Date
    7/1/2021 - 4 years ago
  • Project End Date
    12/31/2022 - 2 years ago
  • Program Officer Name
    MORRIS, JILL A
  • Budget Start Date
    7/1/2021 - 4 years ago
  • Budget End Date
    12/31/2022 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    01
  • Suffix
    A1
  • Award Notice Date
    6/28/2021 - 4 years ago

A versatile reporter for visualization of myelin plasticity in the genetically modified rat

Abstract Myelin structure is a critical regulator of nerve conduction and an essential factor in axon development and homeostasis. In recent years, a number of seminal observations have dispelled a long-standing dogma that myelin is a static, inflexible structure. Advances in imaging techniques as well as in the methods used to label myelin have revealed that myelin plasticity occurs at the level of wrap number and sheath length during post- natal development, aging, and regeneration after injury. Observations of myelin plasticity indicate a more profound role of myelin axon function, and thereby highlight a critical need for better tools to investigate the mechanisms of myelin formation and remodeling. Here, we propose that the limited availability of tools for myelin reporting has significantly hindered our understanding of myelin biology. Illuminating the mechanisms of myelin plasticity will dramatically impact our understanding of the function of myelin in the nervous system and how myelin contributes to aging, injury, and disease. Our lab and others have developed myelin reporter systems in the mouse, but many of the behavioral and physiological studies that could inform myelin function are better modeled in the rat. The rat nervous system is unique from the mouse in terms of critical elements of behavior, endocrine function, epigenetics, and neurogenesis. Rats are also considered superior for modeling and translating regenerative therapies. We propose to develop a versatile myelin membrane reporter system in the rat capable of discriminating between new and old myelin in the nervous system with spatial and temporal precision. To generate the first myelin reporter rat system, we propose: Aim 1: Develop a rat myelin reporter system and Aim 2: Test the specificity and efficiency of myelin promoters in the rat reporter system. Results from this research will produce a myelin tagging system that will have unique functional advantages for the study of myelin development, myelin regeneration, and myelin in aging.

IC Name
NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
  • Activity
    R21
  • Administering IC
    NS
  • Application Type
    1
  • Direct Cost Amount
    275000
  • Indirect Cost Amount
    169125
  • Total Cost
    444125
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    853
  • Ed Inst. Type
  • Funding ICs
    NINDS:444125\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    CMBG
  • Study Section Name
    Cellular and Molecular Biology of Glia Study Section
  • Organization Name
    METHODIST HOSPITAL RESEARCH INSTITUTE
  • Organization Department
  • Organization DUNS
    185641052
  • Organization City
    HOUSTON
  • Organization State
    TX
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    77030
  • Organization District
    UNITED STATES