Expression of receptors for advanced glycosylated end-products in renal disease
M Abel, U Ritthaler, Y Zhang, Y Deng… - Nephrology Dialysis …, 1995 - academic.oup.com
M Abel, U Ritthaler, Y Zhang, Y Deng, AM Schmidt, J Greten, T Sernau, P Wahl, K Andrassy…
Nephrology Dialysis Transplantation, 1995•academic.oup.comAbstract Background Advanced glycation endproducts (AGEs) are believed to mediate long-
term complications in diabetes mellitus. In this context we studied the expression of the
receptor for AGEs (RAGE) in the kidney of patients with a variety of different renal diseases.
Methods RAGE was detected by immunocytochemistry in renal biopsies. We compared the
staining for RAGE in nine patients with diabetic nephropathy, 20 with inflammatory and/or
immune complex and 10 with non-inflammatory renal diseases. Normal renal tissue from …
term complications in diabetes mellitus. In this context we studied the expression of the
receptor for AGEs (RAGE) in the kidney of patients with a variety of different renal diseases.
Methods RAGE was detected by immunocytochemistry in renal biopsies. We compared the
staining for RAGE in nine patients with diabetic nephropathy, 20 with inflammatory and/or
immune complex and 10 with non-inflammatory renal diseases. Normal renal tissue from …
Background
Advanced glycation endproducts (AGEs) are believed to mediate long-term complications in diabetes mellitus. In this context we studied the expression of the receptor for AGEs (RAGE) in the kidney of patients with a variety of different renal diseases.
Methods
RAGE was detected by immunocytochemistry in renal biopsies. We compared the staining for RAGE in nine patients with diabetic nephropathy, 20 with inflammatory and/or immune complex and 10 with non-inflammatory renal diseases. Normal renal tissue from seven patients with tumour nephrectomies served as controls.
Results
In controls the only cells expressing RAGE constitutively were interstitial cells and vascular smooth muscle cells (6/7), while distal tubular cells were rarely positive (1/7). Endothelial cells of arteries/arterioles, glomerular endothelial cells, podocytes, and capsular epithelial cells were consistently negative.
In diabetic nephropathy, inflammatory and/or immune complex, and non-inflammatory renal diseases, all cell types mentioned above became positive for RAGE. Whilst the distribution of RAGE in the tissue was quite similar, staining intensity in inflammatory and/or immune complex diseases was higher than in diabetic nephropathy.
Conclusion
RAGE induction in the kidney is not specific for diabetic nephropathy and occurs in other types of renal diseases as well.
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