RAGE/Diaph1, Diabetes, and Kidney Disease: Mechanisms and Novel Therapeutic Strategies

Abstract

In Year One of the funded grant, we have substantial progress in three critical areas: First, we have established the breeding colonies for all four of the key mouse lines to test the roles of RAGE and DIAPH1 in podocytes and monocytes/macrophages in the pathogenesis of diabetes associated nephropathic changes in the kidney. As detailed in the full progress report, many of these animals (males and females) have already been rendered diabetic and are on time course. Second, we have optimized podocyte isolation procedures as indicated in the grant application. This is a key step which will enable us to probe mechanisms of RAGE and DIAPH1 biology in these cells. Third, Dr. Ramasamy identifies substantial progress in the development and validation of metabolomics and lipidomics assays here at NYU in order to understand detailed mechanisms of the role of these molecules in the diabetic kidney. Taken together, our work in Year 1 ensures that the feasibility of our proposed studies is assured and that through the coming year, our research team will begin to obtain important data to address the questions proposed in our Specific Aims.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2018
Accession Number
AD1063817

Entities

People

  • Ann M. Schmidt
  • Ravichandran Ramasamy

Organizations

  • Grossman School of Medicine

Tags

DTIC Thesaurus Topics

  • Cells
  • Cytoskeleton
  • Department Of Defense
  • Diseases And Disorders
  • Genetics
  • Kidney Diseases
  • Kidneys
  • Macrophages
  • Medical Personnel
  • Metabolic Diseases
  • Metabolism
  • Metabolomics
  • Molecules
  • Myeloid Cells
  • Small Molecules
  • Therapy
  • Vascular Diseases

Readers

  • Molecular and Cellular Biology
  • Research Science/Academic Research