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Enhanced migration and adhesion of peripheral blood neutrophils from SAPHO patients revealed by RNA-Seq
BACKGROUND: SAPHO syndrome is a rare disease characterized by inflammatory lesions on skin and bones. Diversified manifestation and inadequate understanding of etiology has limited its diagnosis and treatment. The co-occurrence of other immune-mediated diseases strongly suggests an involvement of au...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688242/ https://www.ncbi.nlm.nih.gov/pubmed/31395074 http://dx.doi.org/10.1186/s13023-019-1169-3 |
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author | Sun, Yuxiu Li, Chen Zhu, Mengmeng Zhang, Shen Cao, Yihan Yang, Qiao Zhao, Pengfei Huang, Guangrui Xu, Anlong |
author_facet | Sun, Yuxiu Li, Chen Zhu, Mengmeng Zhang, Shen Cao, Yihan Yang, Qiao Zhao, Pengfei Huang, Guangrui Xu, Anlong |
author_sort | Sun, Yuxiu |
collection | PubMed |
description | BACKGROUND: SAPHO syndrome is a rare disease characterized by inflammatory lesions on skin and bones. Diversified manifestation and inadequate understanding of etiology has limited its diagnosis and treatment. The co-occurrence of other immune-mediated diseases strongly suggests an involvement of autoimmunity in SAPHO syndrome. However, the role of the largest population of circulating immune cells, neutrophils, is still not well explored. In this study, we performed RNA sequencing to profile the mRNA expression of neutrophils purified from peripheral blood of SAPHO patients to identify key genes associated with SAPHO syndrome, trying to find new functional molecules or biomarkers for this rare disease. RESULTS: A total of 442 differentially expressed genes were identified (p < 0.05, fold change > 2), in which 294 genes were upregulated and 148 genes were downregulated. Five differentially expressed genes of interest were verified by quantitative Real-Time Polymerase Chain Reaction (qRT-PCR), among which S100A12 was upregulated and positively related to high-sensitivity C-reactive protein (hsCRP), while the downregulated gene MYADM was positively related to osteocalcin. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis showed that differentially expressed genes were enriched in “systemic lupus erythematosus” and “ECM-receptor interaction”. Gene ontology (GO) enrichment showed that differentially expressed genes may participate in biological processes such as “cell migration” and “cell adhesion”. CONCLUSIONS: In conclusion, this study provides a first insight into transcriptome characteristics of SAPHO syndrome, indicating an over-active neutrophil recruitment in patients and possibly suggesting molecular candidates for further study on diagnosis and pathology of this disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-019-1169-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6688242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66882422019-08-14 Enhanced migration and adhesion of peripheral blood neutrophils from SAPHO patients revealed by RNA-Seq Sun, Yuxiu Li, Chen Zhu, Mengmeng Zhang, Shen Cao, Yihan Yang, Qiao Zhao, Pengfei Huang, Guangrui Xu, Anlong Orphanet J Rare Dis Research BACKGROUND: SAPHO syndrome is a rare disease characterized by inflammatory lesions on skin and bones. Diversified manifestation and inadequate understanding of etiology has limited its diagnosis and treatment. The co-occurrence of other immune-mediated diseases strongly suggests an involvement of autoimmunity in SAPHO syndrome. However, the role of the largest population of circulating immune cells, neutrophils, is still not well explored. In this study, we performed RNA sequencing to profile the mRNA expression of neutrophils purified from peripheral blood of SAPHO patients to identify key genes associated with SAPHO syndrome, trying to find new functional molecules or biomarkers for this rare disease. RESULTS: A total of 442 differentially expressed genes were identified (p < 0.05, fold change > 2), in which 294 genes were upregulated and 148 genes were downregulated. Five differentially expressed genes of interest were verified by quantitative Real-Time Polymerase Chain Reaction (qRT-PCR), among which S100A12 was upregulated and positively related to high-sensitivity C-reactive protein (hsCRP), while the downregulated gene MYADM was positively related to osteocalcin. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis showed that differentially expressed genes were enriched in “systemic lupus erythematosus” and “ECM-receptor interaction”. Gene ontology (GO) enrichment showed that differentially expressed genes may participate in biological processes such as “cell migration” and “cell adhesion”. CONCLUSIONS: In conclusion, this study provides a first insight into transcriptome characteristics of SAPHO syndrome, indicating an over-active neutrophil recruitment in patients and possibly suggesting molecular candidates for further study on diagnosis and pathology of this disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-019-1169-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-08 /pmc/articles/PMC6688242/ /pubmed/31395074 http://dx.doi.org/10.1186/s13023-019-1169-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Sun, Yuxiu Li, Chen Zhu, Mengmeng Zhang, Shen Cao, Yihan Yang, Qiao Zhao, Pengfei Huang, Guangrui Xu, Anlong Enhanced migration and adhesion of peripheral blood neutrophils from SAPHO patients revealed by RNA-Seq |
title | Enhanced migration and adhesion of peripheral blood neutrophils from SAPHO patients revealed by RNA-Seq |
title_full | Enhanced migration and adhesion of peripheral blood neutrophils from SAPHO patients revealed by RNA-Seq |
title_fullStr | Enhanced migration and adhesion of peripheral blood neutrophils from SAPHO patients revealed by RNA-Seq |
title_full_unstemmed | Enhanced migration and adhesion of peripheral blood neutrophils from SAPHO patients revealed by RNA-Seq |
title_short | Enhanced migration and adhesion of peripheral blood neutrophils from SAPHO patients revealed by RNA-Seq |
title_sort | enhanced migration and adhesion of peripheral blood neutrophils from sapho patients revealed by rna-seq |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688242/ https://www.ncbi.nlm.nih.gov/pubmed/31395074 http://dx.doi.org/10.1186/s13023-019-1169-3 |
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