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.

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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