Targeted proteomics of isolated glomeruli from the kidneys of diabetic rats: sorbin and SH3 domain containing 2 is a novel protein associated with diabetic nephropathy

Exp Diabetes Res. 2011:2011:979354. doi: 10.1155/2011/979354. Epub 2011 Oct 5.

Abstract

To evaluate proteins associated with the development of diabetic nephropathy, a major cause of the end-stage renal disease, we analyzed protein expression in isolated glomeruli from spontaneous type 2 diabetic (OLETF) rats and their age-matched control littermates (LETO) in the early and proteinuric stages of diabetic nephropathy using QSTAR Elite LC-MS/MS. Among the 191 and 218 proteins that were altered significantly in the OLETF rats, twenty-four were actin cytoskeleton-associated proteins implicated in the formation of stress fibers, and the impairment of actin polymerization, intermediate filaments and microtubules. Importantly, sorbin and SH3 domain containing 2 (SORBS2), which is involved in the formation of stress fibers, was significantly upregulated in both stages of diabetic nephropathy (1.49- and 1.97-fold, resp.). Immunohistochemical and quantitative-PCR analyses revealed upregulation of SORBS2 in podocytes of glomeruli of OLETF rats. Our findings suggested that SORBS2 may be associated with the development of diabetic nephropathy possibility by reorganization of actin filaments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Diabetes Mellitus, Type 2 / complications*
  • Diabetic Nephropathies / metabolism*
  • Diabetic Nephropathies / pathology
  • Diabetic Nephropathies / physiopathology
  • Diabetic Nephropathies / urine
  • Disease Progression
  • Down-Regulation
  • Immunohistochemistry
  • Kidney Glomerulus / metabolism*
  • Kidney Glomerulus / ultrastructure
  • Microfilament Proteins / genetics
  • Microfilament Proteins / metabolism
  • Peptide Fragments / chemistry
  • Peptide Fragments / metabolism
  • Podocytes / metabolism
  • Podocytes / ultrastructure
  • Proteinuria / etiology
  • Proteomics / methods*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Inbred OLETF
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Up-Regulation*

Substances

  • Adaptor Proteins, Signal Transducing
  • Microfilament Proteins
  • Peptide Fragments
  • RNA, Messenger
  • Sorbs2 protein, rat