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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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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. |
format | Online Article Text |
id | pubmed-5448067 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
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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