Microalbuminuria in type 1 diabetes is associated with enhanced excretion of the endocytic multiligand receptors megalin and cubilin

Diabetes Care. 2009 Jul;32(7):1266-8. doi: 10.2337/dc09-0112. Epub 2009 Apr 14.

Abstract

Objective: Proteinuria is the hallmark of diabetic nephropathy; yet, glomerular histology does not fully explain mechanisms contributing to proteinuria. Our objective was to identify proteins in the urine of individuals with type 1 diabetes and microalbuminuria that might implicate a mechanistic pathway operative in proteinuria.

Research design and methods: Using a GeLC/MS platform proteomics approach, we compared the urine proteome from 12 healthy nondiabetic individuals, 12 subjects with type 1 diabetes yet normal urinary albumin excretion rates, and 12 subjects with type 1 diabetes and microalbuminuria (type 1 diabetes + microalbuminuria).

Results: The abundance of megalin and cubilin, two multiligand receptors expressed in kidney proximal tubule cells and involved with the reuptake of filtered albumin and megalin/cubilin ligands, was significantly increased in type 1 diabetes + microalbuminuria urine, compared with both nonalbuminuric groups.

Conclusions: Aberrant shedding of megalin and cubilin could contribute to albuminuria in diabetes and to deficiency states of important vitamins and hormones.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / urine*
  • Albuminuria / epidemiology
  • Albuminuria / etiology*
  • Albuminuria / urine
  • Blood Pressure
  • Diabetes Mellitus, Type 1 / urine*
  • Diabetic Nephropathies / urine
  • Female
  • Glomerular Filtration Rate
  • Humans
  • Low Density Lipoprotein Receptor-Related Protein-2
  • Male
  • Proteomics / methods
  • Receptors, Cell Surface / metabolism*
  • Reference Values

Substances

  • Adaptor Proteins, Signal Transducing
  • LRP2BP protein, human
  • Low Density Lipoprotein Receptor-Related Protein-2
  • Receptors, Cell Surface
  • intrinsic factor-cobalamin receptor