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Microalbuminuria in type 1 diabetes is associated with enhanced excretion of the endocytic multiligand receptors megalin and cubilin.
- Source :
-
Diabetes care [Diabetes Care] 2009 Jul; Vol. 32 (7), pp. 1266-8. Date of Electronic Publication: 2009 Apr 14. - Publication Year :
- 2009
-
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.<br />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).<br />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.<br />Conclusions: Aberrant shedding of megalin and cubilin could contribute to albuminuria in diabetes and to deficiency states of important vitamins and hormones.
- Subjects :
- Albuminuria epidemiology
Albuminuria urine
Blood Pressure
Diabetic Nephropathies urine
Female
Glomerular Filtration Rate
Humans
Low Density Lipoprotein Receptor-Related Protein-2
Male
Proteomics methods
Reference Values
Adaptor Proteins, Signal Transducing urine
Albuminuria etiology
Diabetes Mellitus, Type 1 urine
Receptors, Cell Surface metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1935-5548
- Volume :
- 32
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Diabetes care
- Publication Type :
- Academic Journal
- Accession number :
- 19366958
- Full Text :
- https://doi.org/10.2337/dc09-0112