ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2012
Differential expression of laminin isoforms in diabetic nephropathy and other renal diseases.
Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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10 citing papers in PubMed, 21 citations in OpenAlex.
- The accumulation of methylglyoxal and acrolein impairs arginine homeostasis causing hyperglycemia and renal abnormalities in male zebrafish.Nature communications · 2026Article
- Review
- Diabetes and Renal Complications: An Overview on Pathophysiology, Biomarkers and Therapeutic Interventions.Biomedicines · 2024Review
- Novel biomarkers for prognosticating diabetic kidney disease progression.International urology and nephrology · 2023Review
- Comprehensive analysis ofFrontiers in molecular biosciences · 2022Article
- "Point of no return" in unilateral renal ischemia reperfusion injury in mice.Journal of biomedical science · 2020Article
- A novel biomarker of laminin turnover is associated with disease progression and mortality in chronic kidney disease.PloS one · 2018Article
- A comprehensive analysis and annotation of human normal urinary proteome.Scientific reports · 2017Article
- The Tubulointerstitial Pathophysiology of Progressive Kidney Disease.Advances in chronic kidney disease · 2017Review
- Podocyte-specific VEGF-a gain of function induces nodular glomerulosclerosis in eNOS null mice.Journal of the American Society of Nephrology : JASN · 2014Article
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Authors and funding
7 authors at 5 institutions in 2 countries.
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Abstract
Laminin a non-collagenous glycoprotein is a major component of the renal glomerular basement membrane and mesangium. Thus far eleven distinct chains have been described, permutations of which make up 15 laminin isoforms. Laminin molecules interact with cells and other matrix molecules during organ development and differentiation. We studied the distribution of laminin isoforms in patients with type 1 diabetic nephropathy, membranous nephropathy, membranoproliferative glomerulonephritis and IgA nephropathy/ Henoch-Schönlein purpura. Immunofluorescence microscopic studies with laminin-chain-specific antibodies to the α1, α2, α5, β1, β2 and γ1 chains detected α2, β1 and γ1 chain expression in the normal mesangium and α5, β2 and γ1 in normal glomerular basement membrane. Significantly, constituents of the glomerular basement membrane, α5, β2 and γ1 chains were overexpressed in kidneys with diabetic nephropathy. Initially the constituents of the mesangium increased commensurate with the degree of mesangial expansion and degree of diabetic nephropathy. Reduction in α2 chain intensity was observed with severe mesangial expansion and in the areas of nodular glomerulosclerosis. In addition, with late disease aberrant expression of α2 and β2 chains was observed in the mesangium. Glomerular basement membrane in renal disease overexpressed molecules normally present in that location. In summary, the alterations in basement membrane composition in various renal diseases seem to not only reflect the balance between synthesis and degradation of normal basement membrane constituents, but also their aberrant expression.
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