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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...

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Autores principales: Pu, Jiao, Jia, Mengying, Shi, Wei, Hu, Lulu, Wang, Fang, Niu, Yaqi, Tong, Qiaoying, Gong, Zhongcheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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