Role of vimentin in mammalian cell motility

Information

  • Research Project
  • 10276323
  • ApplicationId
    10276323
  • Core Project Number
    R35GM142963
  • Full Project Number
    1R35GM142963-01
  • Serial Number
    142963
  • FOA Number
    PAR-20-117
  • Sub Project Id
  • Project Start Date
    8/16/2021 - 2 years ago
  • Project End Date
    7/31/2026 - 2 years from now
  • Program Officer Name
    XU, JIANHUA
  • Budget Start Date
    8/16/2021 - 2 years ago
  • Budget End Date
    7/31/2022 - a year ago
  • Fiscal Year
    2021
  • Support Year
    01
  • Suffix
  • Award Notice Date
    8/11/2021 - 2 years ago
Organizations

Role of vimentin in mammalian cell motility

ABSTRACT Cell migration is essential to many fundamental processes, including embryonic development, wound repair, and cancer metastasis. Central to this process is the cellular cytoskeleton comprised of three polymeric networks: F-actin, microtubules, and intermediate filaments (IFs). Vimentin is an IF protein that is essential to the mechanical resilience of cells and regulates cross-talk amongst the cytoskeleton, but its role in how cells squeeze through small pores in tissues is poorly understood. We have shown that loss of vimentin enhances cell motility through three-dimensional 3D micro-fluidic channels and protects the nucleus from damage during migration. Vimentin is thought to play a distinct role in the transfer of forces from cell surface matrix adhesions to the nuclear surface, but new evidence suggests that vimentin may also play a more active role in persistent cell motility via its interactions with actin stress fiber formation and microtubule positioning. Still, the specific mechanisms by which vimentin enables 3D migration through dense tissue remains unclear. This project addresses the overarching question: how does vimentin influence cytoskeletal functions, adhesions with the extracellular matrix, and cell-cell interactions to coordinate 3D cell migration? To address this question, we will pursue three sub-projects. First, we will determine the effects of vimentin in cytoskeletal- mediated 3D cell motility. Second, we will identify vimentin?s role in integrin expression and focal adhesion activation, and third, we will identify the mechanisms by which vimentin mediates collective cell migration through extracellular matrix networks. These studies will be conducted in both 2D and 3D settings to define how changes in the cellular environment impact the critical determinants of cytoskeletal polymers in cell motility. We expected that these projects will determine new functional roles of vimentin in cell migration, which has important implications for understanding healthy tissue maintenance and diseases that progress by the migration of cells through tissues.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R35
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
    250000
  • Indirect Cost Amount
    125000
  • Total Cost
    375000
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIGMS:375000\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    SYRACUSE UNIVERSITY
  • Organization Department
    PHYSICS
  • Organization DUNS
    002257350
  • Organization City
    SYRACUSE
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    132441200
  • Organization District
    UNITED STATES