Expression profiling of endogenous secretory receptor for advanced glycation end products in human organs

被引:126
作者
Cheng, CM
Tsuneyama, K
Kominami, R
Shinohara, H
Sakurai, S
Yonekura, H
Watanabe, T
Takano, Y
Yamamoto, H
Yamamoto, Y
机构
[1] Toyama Med & Pharmaceut Univ, Dept Pathol, COE Program 21, Toyama 9300194, Japan
[2] Kanazawa Med Univ, Dept Anat, Ishikawa, Japan
[3] Kanazawa Univ, Grad Sch Med Sci, Dept Biochem & Mol Vasc Biol, Kanazawa, Ishikawa 920, Japan
基金
日本学术振兴会;
关键词
receptor for advanced glycation end products (RAGE); endogenous secretory RAGE (esRAGE); immunohistochemistry; normal human organs;
D O I
10.1038/modpathol.3800450
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The receptor for advanced glycation end products ( RAGE) is a cell surface multiligand receptor of the immunoglobulin superfamily, which participates in physiological and pathological processes such as neuronal development, diabetes, inflammation, neurodegenerative disorders, and cancer. A novel splice variant of RAGE- endogenous secretory decoy form ( esRAGE) was recently identified and is thought to be a prospective candidate to modify these RAGE- associated conditions. Here, we investigated the expression and distribution of esRAGE and RAGE proteins with domain- specific antibodies. We studied a wide variety of adult normal human preparations obtained from surgical and autopsy specimens using a tissue microarray technique. The results revealed that esRAGE was widely distributed and we classified its expression into four patterns. In pattern A, the cytoplasm is stained diffusely in neurons, vascular endothelium, pneumocytes, mesothelium, pancreatic beta cells, and macrophages/ monocytes. In pattern B, dot- like granules are stained in the supranuclear regions facing the luminal surface of the bile ducts, salivary glands, digestive tracts, renal tubules, prostate, skin, thyroid, and bronchioles. Pattern C is represented by diffuse staining in the stromal area of the arterial walls. Pattern D shows diffuse and strong staining of secreted materials such as thyroidal colloid, crystals in renal tubular lumen, and glandular lumen in prostate. This study provides, for the first time, a histopathological basis for understanding the physiological roles of esRAGE in humans, and will contribute to elucidating the participation of esRAGE in pathological processes and to exploring novel diagnostic and therapeutic concepts.
引用
收藏
页码:1385 / 1396
页数:12
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