Localization and expression pattern of amelotin, odontogenic ameloblast-associated protein and follicular dendritic cell-secreted protein in the junctional epithelium of inflamed gingiva

• Published in: Odontology 2017-07, Vol.105 (3), p.329-337
• Main Authors: Nakayama, Yohei, Kobayashi, Ryoki, Matsui, Sari, Matsumura, Hiroyoshi, Iwai, Yasunobu, Noda, Keisuke, Yamazaki, Mizuho, Kurita-Ochiai, Tomoko, Yoshimura, Atsutoshi, Shinomura, Tamayuki, Ganss, Bernhard, Ogata, Yorimasa
• Format: Article
• Language: English
• Subjects: Aggregatibacter actinomycetemcomitans; Animals; Bacteroidaceae Infections - metabolism; Basal lamina; Dendritic cells; Dental Enamel Proteins - metabolism; Dentistry; Disease Models, Animal; Epithelial Attachment - metabolism; Epithelium; Gingiva; Gingiva - metabolism; Gum disease; Humans; Immunohistochemistry; Inflammation; Inflammation - metabolism; Localization; Medicine; Mice; Oral and Maxillofacial Surgery; Original Article; Pasteurellaceae Infections - metabolism; Periodontitis - metabolism; Porphyromonas gingivalis; Proteins; Proteins - metabolism
• ISSN: 1618-1247; 1618-1255
• DOI: 10.1007/s10266-016-0277-y

[Abstract] The purpose of this study is to elucidate the localization of amelotin (AMTN), odontogenic ameloblast-associated protein (ODAM) and follicular dendritic cell-secreted protein (FDC-SP) at the junctional epithelium (JE) in Porphyromonas gingivalis and Aggregatibacter actinomycetemcomitans infected mice and inflamed and non-inflamed human gingiva. We performed immunostaining to determine the localization and expression pattern of AMTN, ODAM and FDC-SP. AMTN, ODAM and FDC-SP in A. actinomycetemcomitans infected mice did not change dramatically compared with non-infected mice. AMTN and FDC-SP expressions were observed stronger in P. gingivalis infected mice at early stage. However, at the following stage, the coronal part of the AMTN expression disappeared from the JE, and FDC-SP expression decreased due to severe inflammation by P. gingivalis. ODAM expressed internal and external basal lamina, and the expression increased not only at early stage but also at the following stage in the inflammatory JE induced by P. gingivalis. In the human gingival tissues, AMTN was detected at the surface of the sulcular epithelium and JE in the non-inflamed and inflamed gingiva, and the localization did not change the process of inflammation. ODAM and FDC-SP were more widely detected at the sulcular epithelium and JE in the non-inflamed gingiva. In the inflamed gingiva, localization of ODAM and FDC-SP was spread into the gingival epithelium, compared to AMTN. These studies demonstrated that the expression pattern of AMTN, ODAM and FDC-SP at the JE were changed during inflammation process and these three proteins might play an important role in the resistance to inflammation.