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Survey of the distribution of a newly characterized receptor for advanced glycation end products in tissues
J Brett1, A M Schmidt, S D Yan
1Department of Physiology and Cellular Biophysics and Surgery, Columbia University, College of Physicians and Surgeons, New York, New York 10032.
Abstract:
Advanced glycation end products (AGEs), the final products of nonenzymatic glycation and oxidation of proteins, are found in the plasma and accumulate in the tissues during aging and at an accelerated rate in diabetes. A novel integral membrane protein, termed receptor for AGE (RAGE), forms a central part of the cell surface binding site for AGEs. Using monospecific, polyclonal antibody raised to human recombinant and bovine RAGE, immunostaining of bovine tissues showed RAGE in the vasculature, endothelium, and smooth muscle cells and in mononuclear cells in the tissues. Consistent with these data, RAGE antigen and mRNA were identified in cultured bovine endothelium, vascular smooth muscle, and monocyte-derived macrophages. RAGE antigen was also visualized in bovine cardiac myocytes as well as in cultures of neonatal rat cardiac myocytes and in neural tissue where motor neurons, peripheral nerves, and a population of cortical neurons were positive. In situ hybridization confirmed the presence of RAGE mRNA in the tissues, and studies with rat PC12 pheochromocytes indicated that they provide a neuronal-related cell culture model for examining RAGE expression. Pathological studies of human atherosclerotic plaques showed infiltration of RAGE-expressing cells in the expanded intima. These results indicate that RAGE is present in multiple tissues and suggest the potential relevance of AGE-RAGE interactions for modulating properties of the vasculature as well as neural and cardiac function, prominent areas of involvement in diabetes and in the normal aging process.
Insights
Advanced glycation end products (AGEs) bind to the receptor for AGE (RAGE). This study identifies RAGE in various tissues, suggesting its role in aging and diabetes-related vascular, neural, and cardiac conditions.
Area of Science:
- Biochemistry
- Cell Biology
- Pathology
Background:
- Advanced glycation end products (AGEs) are formed through nonenzymatic glycation and oxidation of proteins.
- AGEs accumulate in tissues during aging and are accelerated in diabetes.
- The receptor for AGE (RAGE) is a cell surface protein that binds AGEs.
Purpose of the Study:
- To investigate the presence and distribution of RAGE in various bovine and rat tissues.
- To explore the potential role of AGE-RAGE interactions in physiological and pathological processes.
Main Methods:
- Immunostaining using polyclonal antibodies against RAGE.
- Identification of RAGE antigen and mRNA in cultured cells (endothelium, vascular smooth muscle, macrophages, cardiac myocytes, pheochromocytes).
- In situ hybridization to confirm RAGE mRNA presence in tissues.
- Examination of human atherosclerotic plaques for RAGE-expressing cells.
Main Results:
- RAGE was detected in bovine vasculature, endothelium, smooth muscle cells, and mononuclear cells.
- RAGE antigen and mRNA were found in cultured endothelial cells, vascular smooth muscle cells, and macrophages.
- RAGE was visualized in cardiac myocytes and neural tissues (motor neurons, peripheral nerves, cortical neurons).
- RAGE-expressing cells were observed infiltrating human atherosclerotic plaques.
Conclusions:
- RAGE is expressed in multiple tissues, including vasculature, cardiac, and neural systems.
- AGE-RAGE interactions may influence vascular, neural, and cardiac functions.
- These interactions are potentially relevant to normal aging and diabetes complications.
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