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Expression of ICOS in the salivary glands of patients with primary Sjogren's syndrome and its molecular mechanism
The present study aimed to explore latent markers for identifying primary Sjogren's syndrome (pSS), as well as their expression and molecular mechanism. Hub inducible T cell co-stimulator genes were retrieved from the Gene Expression Omnibus. A total of 95 patients with pSS and 68 healthy indiv...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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D.A. Spandidos
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551409/ https://www.ncbi.nlm.nih.gov/pubmed/36177915 http://dx.doi.org/10.3892/mmr.2022.12864 |
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author | Li, Ping Jin, Yi Zhao, Rui Xue, Zhonghui Ji, Juan |
author_facet | Li, Ping Jin, Yi Zhao, Rui Xue, Zhonghui Ji, Juan |
author_sort | Li, Ping |
collection | PubMed |
description | The present study aimed to explore latent markers for identifying primary Sjogren's syndrome (pSS), as well as their expression and molecular mechanism. Hub inducible T cell co-stimulator genes were retrieved from the Gene Expression Omnibus. A total of 95 patients with pSS and 68 healthy individuals from Affiliated Hospital of Nantong University (Nantong, China) were included in the study. The expression of inducible T cell co-stimulator (ICOS) in whole blood and saliva was evaluated using ELISA. Western blotting was performed to investigate aquaporin 5 (AQP5) protein expression, as well as the inflammatory effects of ICOS in patients with pSS compared with healthy individuals. Differentially expressed mRNAs were analyzed in whole blood (GSE84844) and salivary gland (GSE40611) of patients with pSS. In total, 15 hub genes were identified, among which ICOS was indicated to serve a role in the most pivotal immunity pathways. pSS was markedly associated with inflammatory pathways. Results from the present study found that ICOS was upregulated in the salivary gland, whole blood and saliva of patients with pSS. Salivary weight was negatively correlated with the levels of ICOS in the saliva of patients with pSS. The expression of AQP5 was markedly lower in patients with pSS. The expression of AQP5 was negatively associated with ICOS. Compared with that of healthy individuals, the expression of ICOS and inflammatory factors was higher and the expression of AQP5 was lower in pSS patients as assessed by western blotting. These data demonstrated that ICOS may affect AQP5 expression by promoting inflammation in the salivary glands of patients with pSS. |
format | Online Article Text |
id | pubmed-9551409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-95514092022-10-15 Expression of ICOS in the salivary glands of patients with primary Sjogren's syndrome and its molecular mechanism Li, Ping Jin, Yi Zhao, Rui Xue, Zhonghui Ji, Juan Mol Med Rep Articles The present study aimed to explore latent markers for identifying primary Sjogren's syndrome (pSS), as well as their expression and molecular mechanism. Hub inducible T cell co-stimulator genes were retrieved from the Gene Expression Omnibus. A total of 95 patients with pSS and 68 healthy individuals from Affiliated Hospital of Nantong University (Nantong, China) were included in the study. The expression of inducible T cell co-stimulator (ICOS) in whole blood and saliva was evaluated using ELISA. Western blotting was performed to investigate aquaporin 5 (AQP5) protein expression, as well as the inflammatory effects of ICOS in patients with pSS compared with healthy individuals. Differentially expressed mRNAs were analyzed in whole blood (GSE84844) and salivary gland (GSE40611) of patients with pSS. In total, 15 hub genes were identified, among which ICOS was indicated to serve a role in the most pivotal immunity pathways. pSS was markedly associated with inflammatory pathways. Results from the present study found that ICOS was upregulated in the salivary gland, whole blood and saliva of patients with pSS. Salivary weight was negatively correlated with the levels of ICOS in the saliva of patients with pSS. The expression of AQP5 was markedly lower in patients with pSS. The expression of AQP5 was negatively associated with ICOS. Compared with that of healthy individuals, the expression of ICOS and inflammatory factors was higher and the expression of AQP5 was lower in pSS patients as assessed by western blotting. These data demonstrated that ICOS may affect AQP5 expression by promoting inflammation in the salivary glands of patients with pSS. D.A. Spandidos 2022-09-28 /pmc/articles/PMC9551409/ /pubmed/36177915 http://dx.doi.org/10.3892/mmr.2022.12864 Text en Copyright: © Li et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , 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 | Articles Li, Ping Jin, Yi Zhao, Rui Xue, Zhonghui Ji, Juan Expression of ICOS in the salivary glands of patients with primary Sjogren's syndrome and its molecular mechanism |
title | Expression of ICOS in the salivary glands of patients with primary Sjogren's syndrome and its molecular mechanism |
title_full | Expression of ICOS in the salivary glands of patients with primary Sjogren's syndrome and its molecular mechanism |
title_fullStr | Expression of ICOS in the salivary glands of patients with primary Sjogren's syndrome and its molecular mechanism |
title_full_unstemmed | Expression of ICOS in the salivary glands of patients with primary Sjogren's syndrome and its molecular mechanism |
title_short | Expression of ICOS in the salivary glands of patients with primary Sjogren's syndrome and its molecular mechanism |
title_sort | expression of icos in the salivary glands of patients with primary sjogren's syndrome and its molecular mechanism |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551409/ https://www.ncbi.nlm.nih.gov/pubmed/36177915 http://dx.doi.org/10.3892/mmr.2022.12864 |
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