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Immunohistochemical analysis of pyroptosis‐related protein expression in IgG4‐related sialadenitis
BACKGROUND: NLRP3 (NOD‐, LRR‐ and pyrin domain‐containing protein 3)‐induced pyroptosis is involved in the development of a variety of autoimmune diseases, but its role in IgG4‐related sialadenitis (IgG4‐RS) is unclear. METHODS: Salivary gland tissues from 19 patients with IgG4‐RS were designated th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310745/ https://www.ncbi.nlm.nih.gov/pubmed/35218237 http://dx.doi.org/10.1111/jop.13290 |
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author | Pu, Jiao Jia, Mengying Shi, Wei Hu, Lulu Wang, Fang Niu, Yaqi Tong, Qiaoying Gong, Zhongcheng |
author_facet | Pu, Jiao Jia, Mengying Shi, Wei Hu, Lulu Wang, Fang Niu, Yaqi Tong, Qiaoying Gong, Zhongcheng |
author_sort | Pu, Jiao |
collection | PubMed |
description | BACKGROUND: NLRP3 (NOD‐, LRR‐ and pyrin domain‐containing protein 3)‐induced pyroptosis is involved in the development of a variety of autoimmune diseases, but its role in IgG4‐related sialadenitis (IgG4‐RS) is unclear. METHODS: Salivary gland tissues from 19 patients with IgG4‐RS were designated the experimental group, and peritumoral tissues from 20 patients with benign salivary gland tumours were designated the control group. The cell morphology and fibrosis in the IgG4‐RS samples were observed by haematoxylin‐eosin (H&E) and Masson trichrome (MT) staining. Immunohistochemical (IHC) staining was used to determine pyroptosis‐related proteins (NLRP3, ASC (apoptosis‐associated speck‐like protein containing a CARD), Caspase‐1, GSDMD (gasdermin family members, including digestive dermatin D), interleukin 1β (IL‐1β), and interleukin 18 (IL‐18)) expression levels. RESULTS: Increased lymphoid follicle proliferation, germinal centre plasma cell infiltration, and irregular fibrosis were observed in the experimental group compared with the control group. The NLRP3, ASC, Caspase‐1, GSDMD, IL‐1β, and IL‐18 levels were significantly higher in the experimental group than in the control group (p < 0.0001). CONCLUSION: This study suggested that pyroptosis‐related proteins might be involved in IgG4‐RS pathogenesis. However, the specific cellular pathway involved and whether multiple cell death pathways contribute to the occurrence of IgG4‐RS still need to be further studied. |
format | Online Article Text |
id | pubmed-9310745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93107452022-07-29 Immunohistochemical analysis of pyroptosis‐related protein expression in IgG4‐related sialadenitis Pu, Jiao Jia, Mengying Shi, Wei Hu, Lulu Wang, Fang Niu, Yaqi Tong, Qiaoying Gong, Zhongcheng J Oral Pathol Med Original Articles BACKGROUND: NLRP3 (NOD‐, LRR‐ and pyrin domain‐containing protein 3)‐induced pyroptosis is involved in the development of a variety of autoimmune diseases, but its role in IgG4‐related sialadenitis (IgG4‐RS) is unclear. METHODS: Salivary gland tissues from 19 patients with IgG4‐RS were designated the experimental group, and peritumoral tissues from 20 patients with benign salivary gland tumours were designated the control group. The cell morphology and fibrosis in the IgG4‐RS samples were observed by haematoxylin‐eosin (H&E) and Masson trichrome (MT) staining. Immunohistochemical (IHC) staining was used to determine pyroptosis‐related proteins (NLRP3, ASC (apoptosis‐associated speck‐like protein containing a CARD), Caspase‐1, GSDMD (gasdermin family members, including digestive dermatin D), interleukin 1β (IL‐1β), and interleukin 18 (IL‐18)) expression levels. RESULTS: Increased lymphoid follicle proliferation, germinal centre plasma cell infiltration, and irregular fibrosis were observed in the experimental group compared with the control group. The NLRP3, ASC, Caspase‐1, GSDMD, IL‐1β, and IL‐18 levels were significantly higher in the experimental group than in the control group (p < 0.0001). CONCLUSION: This study suggested that pyroptosis‐related proteins might be involved in IgG4‐RS pathogenesis. However, the specific cellular pathway involved and whether multiple cell death pathways contribute to the occurrence of IgG4‐RS still need to be further studied. John Wiley and Sons Inc. 2022-03-09 2022-04 /pmc/articles/PMC9310745/ /pubmed/35218237 http://dx.doi.org/10.1111/jop.13290 Text en © 2022 The Authors. Journal of Oral Pathology & Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Pu, Jiao Jia, Mengying Shi, Wei Hu, Lulu Wang, Fang Niu, Yaqi Tong, Qiaoying Gong, Zhongcheng Immunohistochemical analysis of pyroptosis‐related protein expression in IgG4‐related sialadenitis |
title | Immunohistochemical analysis of pyroptosis‐related protein expression in IgG4‐related sialadenitis |
title_full | Immunohistochemical analysis of pyroptosis‐related protein expression in IgG4‐related sialadenitis |
title_fullStr | Immunohistochemical analysis of pyroptosis‐related protein expression in IgG4‐related sialadenitis |
title_full_unstemmed | Immunohistochemical analysis of pyroptosis‐related protein expression in IgG4‐related sialadenitis |
title_short | Immunohistochemical analysis of pyroptosis‐related protein expression in IgG4‐related sialadenitis |
title_sort | immunohistochemical analysis of pyroptosis‐related protein expression in igg4‐related sialadenitis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310745/ https://www.ncbi.nlm.nih.gov/pubmed/35218237 http://dx.doi.org/10.1111/jop.13290 |
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