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High Expression of Galectin-3 in Patients with IgG4-Related Disease: A Proteomic Approach

OBJECTIVES: Immunoglobulin G4-related disease (IgG4-RD) is a multiorgan condition manifesting itself in different forms. This study aimed to investigate protein expression profiles and to find the possible biomarker for IgG4-RD by liquid chromatography mass spectrometry (LC-MS) using tissue sections...

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Autores principales: Salah, Adeeb, Yoshifuji, Hajime, Ito, Shinji, Kitagori, Koji, Kiso, Kaori, Yamada, Norishige, Nakajima, Toshiki, Haga, Hironori, Tsuruyama, Tatsuaki, Miyagawa-Hayashino, Aya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448067/
https://www.ncbi.nlm.nih.gov/pubmed/28593065
http://dx.doi.org/10.1155/2017/9312142
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author Salah, Adeeb
Yoshifuji, Hajime
Ito, Shinji
Kitagori, Koji
Kiso, Kaori
Yamada, Norishige
Nakajima, Toshiki
Haga, Hironori
Tsuruyama, Tatsuaki
Miyagawa-Hayashino, Aya
author_facet Salah, Adeeb
Yoshifuji, Hajime
Ito, Shinji
Kitagori, Koji
Kiso, Kaori
Yamada, Norishige
Nakajima, Toshiki
Haga, Hironori
Tsuruyama, Tatsuaki
Miyagawa-Hayashino, Aya
author_sort Salah, Adeeb
collection PubMed
description OBJECTIVES: Immunoglobulin G4-related disease (IgG4-RD) is a multiorgan condition manifesting itself in different forms. This study aimed to investigate protein expression profiles and to find the possible biomarker for IgG4-RD by liquid chromatography mass spectrometry (LC-MS) using tissue sections in IgG4-RD patients. METHODS: Protein expression profiles in five IgG4-related pancreatitis and three normal pancreatic samples were compared using LC-MS and were validated by quantitative real-time PCR (qRT-PCR), immunoblotting, and immunohistochemistry. ELISA was employed in the serum of 20 patients with systemic IgG4-RD before and during steroid treatment. RESULTS: LC-MS indicated that the levels of 17 proteins were significantly higher and 12 others were significantly lower in IgG4-related pancreatitis patients compared to controls. Among these proteins, galectin-3 levels were 13-fold higher in IgG4-related pancreatitis (P < 0.01). These results were confirmed by immunoblotting and qRT-PCR. The average number of galectin-3 + cells in various organs of IgG4-RD patients, including salivary glands, lungs, and lymph nodes, was higher than in controls. Galectin-3 was detectable in macrophages, dendritic cells, and stromal myofibroblast-like cells, but not in lymphocytes by immunofluorescence staining. Serum galectin-3 levels were higher in patients with IgG4-RD compared with healthy donors and remained high during steroid therapy. CONCLUSION: Galectin-3 was overexpressed in IgG4-RD and the levels were indirectly related to clinical activity.
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spelling pubmed-54480672017-06-07 High Expression of Galectin-3 in Patients with IgG4-Related Disease: A Proteomic Approach Salah, Adeeb Yoshifuji, Hajime Ito, Shinji Kitagori, Koji Kiso, Kaori Yamada, Norishige Nakajima, Toshiki Haga, Hironori Tsuruyama, Tatsuaki Miyagawa-Hayashino, Aya Patholog Res Int Research Article OBJECTIVES: Immunoglobulin G4-related disease (IgG4-RD) is a multiorgan condition manifesting itself in different forms. This study aimed to investigate protein expression profiles and to find the possible biomarker for IgG4-RD by liquid chromatography mass spectrometry (LC-MS) using tissue sections in IgG4-RD patients. METHODS: Protein expression profiles in five IgG4-related pancreatitis and three normal pancreatic samples were compared using LC-MS and were validated by quantitative real-time PCR (qRT-PCR), immunoblotting, and immunohistochemistry. ELISA was employed in the serum of 20 patients with systemic IgG4-RD before and during steroid treatment. RESULTS: LC-MS indicated that the levels of 17 proteins were significantly higher and 12 others were significantly lower in IgG4-related pancreatitis patients compared to controls. Among these proteins, galectin-3 levels were 13-fold higher in IgG4-related pancreatitis (P < 0.01). These results were confirmed by immunoblotting and qRT-PCR. The average number of galectin-3 + cells in various organs of IgG4-RD patients, including salivary glands, lungs, and lymph nodes, was higher than in controls. Galectin-3 was detectable in macrophages, dendritic cells, and stromal myofibroblast-like cells, but not in lymphocytes by immunofluorescence staining. Serum galectin-3 levels were higher in patients with IgG4-RD compared with healthy donors and remained high during steroid therapy. CONCLUSION: Galectin-3 was overexpressed in IgG4-RD and the levels were indirectly related to clinical activity. Hindawi 2017 2017-05-16 /pmc/articles/PMC5448067/ /pubmed/28593065 http://dx.doi.org/10.1155/2017/9312142 Text en Copyright © 2017 Adeeb Salah et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Salah, Adeeb
Yoshifuji, Hajime
Ito, Shinji
Kitagori, Koji
Kiso, Kaori
Yamada, Norishige
Nakajima, Toshiki
Haga, Hironori
Tsuruyama, Tatsuaki
Miyagawa-Hayashino, Aya
High Expression of Galectin-3 in Patients with IgG4-Related Disease: A Proteomic Approach
title High Expression of Galectin-3 in Patients with IgG4-Related Disease: A Proteomic Approach
title_full High Expression of Galectin-3 in Patients with IgG4-Related Disease: A Proteomic Approach
title_fullStr High Expression of Galectin-3 in Patients with IgG4-Related Disease: A Proteomic Approach
title_full_unstemmed High Expression of Galectin-3 in Patients with IgG4-Related Disease: A Proteomic Approach
title_short High Expression of Galectin-3 in Patients with IgG4-Related Disease: A Proteomic Approach
title_sort high expression of galectin-3 in patients with igg4-related disease: a proteomic approach
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5448067/
https://www.ncbi.nlm.nih.gov/pubmed/28593065
http://dx.doi.org/10.1155/2017/9312142
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