Involvement of inducible nitric oxide synthase and receptor for advanced glycation end products in periapical granulomas

被引:20
|
作者
Hama, Shinji
Takeichi, Osamu
Saito, Ichiro
Ito, Koichi
机构
[1] Nihon Univ, Sch Dent, Dept Endodont, Chiyoda Ku, Tokyo 1018310, Japan
[2] Nihon Univ, Sch Dent, Dent Res Ctr, Div Adv Dent Treatment, Tokyo, Japan
[3] Tsurumi Univ, Sch Dent Med, Dept Pathol, Yokohama, Kanagawa, Japan
[4] Nihon Univ, Sch Dent, Dent Res Ctr, Div Adv Dent Treatment, Tokyo 1018310, Japan
[5] Nihon Univ, Sch Dent, Dept Periodontol, Tokyo 1018310, Japan
关键词
immunohistochemistry; inducible nitric oxide synthase; periapical granulomas; periapical periodontitis; receptor for advanced glycation end products;
D O I
10.1016/j.joen.2006.11.011
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
We examined the presence of the receptor for advanced glycation end products (RAGE) in periapical granulomas and analyzed the interaction between RAGE and inducible nitric oxide synthase (iNOS) to elucidate inflammatory reaction mechanisms. Periapical lesions were surgically removed from 37 patients with chronic periapical periodontitis and halved, Paraffin sections were prepared from half of each lesion and stained with hematoxylin and eosin, whereas cryostat sections were prepared from the other half. Based on the histological evaluation, 33 of the lesions were diagnosed as periapical granulomas. These were examined by immunohistochemistry using serial cryostat sections probed with anti-human iNOS or RAGE antibodies. Macrophages, lymphocytes, and endothelial cells expressed RAGE and these cell types, in addition to plasma cells, exhibited anti-iNOS immunoreactivity. Serial cryostat sections demonstrated the infiltration of RAGE-expressing cells around iNOS-producing cells, suggesting that these molecules may be important in the tissue injury associated with periapical periodontitis.
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页码:137 / 141
页数:5
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