PROTEIN-MINERAL INTERACTIONS AND CALCIUM OXALATE STONES

Information

  • Research Project
  • 7216704
  • ApplicationId
    7216704
  • Core Project Number
    R01DK064050
  • Full Project Number
    5R01DK064050-04
  • Serial Number
    64050
  • FOA Number
    PA-03-65
  • Sub Project Id
  • Project Start Date
    4/1/2004 - 20 years ago
  • Project End Date
    3/31/2009 - 15 years ago
  • Program Officer Name
    RASOOLY, REBEKAH S.
  • Budget Start Date
    4/1/2007 - 17 years ago
  • Budget End Date
    3/31/2008 - 16 years ago
  • Fiscal Year
    2007
  • Support Year
    4
  • Suffix
  • Award Notice Date
    4/9/2007 - 17 years ago

PROTEIN-MINERAL INTERACTIONS AND CALCIUM OXALATE STONES

DESCRIPTION (provided by applicant): Urolithiasis is a serious, debilitating and costly problem in societies throughout the world. The role of urinary proteins in calcium oxalate (CaOx) kidney stone formation, particularly intracrystalline proteins, remains a mystery. The planned work will clarify the role of superficial and intracrystalline CaOx proteins, especially OPN and UPTF1, in the attachment of urinary crystals to renal epithelial cells, as well as their subsequent disintegration and dissolution. Using a Madin-Darby canine kidney (MDCK) cell line model of crystal-cell interaction, the studies will: (1) determine the effects of intracrystalline and surface-bound OPN and UPTF1 on the binding, phagocytosis, intracellular disintegration and dissolution of CaOx crystals. (2) (a) identify which lysosomal proteases digest intracrystalline OPN and UPTF1 and (b) determine the effects of crystal phagocytosis on their individual specific activities, as well as that of total protease specific activity. (3) (a) determine the effects of intracrystalline OPN and UPTF1 on the gene expression (mRNA) of individual proteases identified in Aim 2 and on the gene expression (mRNA) and further cellular production of UPTF1 and OPN. (b) Determine the effects of [Ca] and [Ox] on the gene expression (mRNA) of OPN and UPTFI. (4) (a) compare the ability of urinary CaOx crystals from male and female stone formers and controls to be bound, phagocytosed and destroyed intracellularly; (b) determine the effects of those crystals on the specific activity and cellular synthesis of the lysosomal enzymes identified in Aim 2, as well as the cellular synthesis of OPN and UPTF1; (c) quantify the urinary activities of those enzymes in stone formers and healthy subjects. The proposed studies will use a combination of cell culture, high-resolution microscopy, enzymatic analysis, protein chemistry and molecular biological techniques. The data generated will offer boundless promise in the design of drugs for stone prophylaxis, the construction of porous crystals for medical and industrial applications, and for understanding the cycle of biomineral formation, destruction and reclamation throughout the natural world.

IC Name
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
  • Activity
    R01
  • Administering IC
    DK
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    176252
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    849
  • Ed Inst. Type
  • Funding ICs
    NIDDK:176252\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    FLINDERS UNIVERSITY OF SOUTH AUSTRALIA
  • Organization Department
  • Organization DUNS
  • Organization City
    ADELAIDE
  • Organization State
  • Organization Country
    AUSTRALIA
  • Organization Zip Code
    5001
  • Organization District
    AUSTRALIA