Identification of CD14 and lipopolysaccharide-binding protein as novel biomarkers for sarcoidosis using proteomics of serum extracellular vesicles. (16th March 2022)
- Record Type:
- Journal Article
- Title:
- Identification of CD14 and lipopolysaccharide-binding protein as novel biomarkers for sarcoidosis using proteomics of serum extracellular vesicles. (16th March 2022)
- Main Title:
- Identification of CD14 and lipopolysaccharide-binding protein as novel biomarkers for sarcoidosis using proteomics of serum extracellular vesicles
- Authors:
- Futami, Yu
Takeda, Yoshito
Koba, Taro
Narumi, Ryohei
Nojima, Yosui
Ito, Mari
Nakayama, Mana
Ishida, Mimiko
Yoshimura, Hanako
Naito, Yujiro
Fukushima, Kiyoharu
Takimoto, Takayuki
Edahiro, Ryuya
Matsuki, Takanori
Nojima, Satoshi
Hirata, Haruhiko
Koyama, Shohei
Iwahori, Kota
Nagatomo, Izumi
Shirai, Yuya
Suga, Yasuhiko
Satoh, Shingo
Futami, Shinji
Miyake, Kotaro
Shiroyama, Takayuki
Inoue, Yoshikazu
Adachi, Jun
Tomonaga, Takeshi
Ueda, Koji
Kumanogoh, Atsushi - Abstract:
- Abstract: Sarcoidosis is a complex, polygenic, inflammatory granulomatous multi-organ disease of unknown cause. The granulomatous inflammation in sarcoidosis is driven by the interplay between T cells and macrophages. Extracellular vesicles (EVs) play important roles in intercellular communication. We subjected serum EVs, isolated by size exclusion chromatography, from seven patients with sarcoidosis and five control subjects to non-targeted proteomics analysis. Non-targeted, label-free proteomics analysis detected 2292 proteins in serum EVs; 42 proteins were up-regulated in patients with sarcoidosis relative to control subjects; and 324 proteins were down-regulated. The protein signature of EVs from patients with sarcoidosis reflected disease characteristics such as antigen presentation and immunological disease. Candidate biomarkers were further verified by targeted proteomics analysis (selected reaction monitoring) in 46 patients and 10 control subjects. Notably, CD14 and lipopolysaccharide-binding protein (LBP) were validated by targeted proteomics analysis. Up-regulation of these proteins was further confirmed by immunoblotting, and their expression was strongly increased in macrophages of lung granulomatous lesions. Consistent with these findings, CD14 levels were increased in lipopolysaccharide-stimulated macrophages during multinucleation, concomitant with increased levels of CD14 and LBP in EVs. The area under the curve values of CD14 and LBP were 0.81 and 0.84,Abstract: Sarcoidosis is a complex, polygenic, inflammatory granulomatous multi-organ disease of unknown cause. The granulomatous inflammation in sarcoidosis is driven by the interplay between T cells and macrophages. Extracellular vesicles (EVs) play important roles in intercellular communication. We subjected serum EVs, isolated by size exclusion chromatography, from seven patients with sarcoidosis and five control subjects to non-targeted proteomics analysis. Non-targeted, label-free proteomics analysis detected 2292 proteins in serum EVs; 42 proteins were up-regulated in patients with sarcoidosis relative to control subjects; and 324 proteins were down-regulated. The protein signature of EVs from patients with sarcoidosis reflected disease characteristics such as antigen presentation and immunological disease. Candidate biomarkers were further verified by targeted proteomics analysis (selected reaction monitoring) in 46 patients and 10 control subjects. Notably, CD14 and lipopolysaccharide-binding protein (LBP) were validated by targeted proteomics analysis. Up-regulation of these proteins was further confirmed by immunoblotting, and their expression was strongly increased in macrophages of lung granulomatous lesions. Consistent with these findings, CD14 levels were increased in lipopolysaccharide-stimulated macrophages during multinucleation, concomitant with increased levels of CD14 and LBP in EVs. The area under the curve values of CD14 and LBP were 0.81 and 0.84, respectively, and further increased to 0.98 in combination with angiotensin-converting enzyme and soluble interleukin-2 receptor. These findings suggest that CD14 and LBP in serum EVs, which are associated with granulomatous pathogenesis, can improve the diagnostic accuracy in patients with sarcoidosis. Abstract : Proteomics of extracellular vesicles reveals new sarcoidosis biomarkers Graphical Abstract: … (more)
- Is Part Of:
- International immunology. Volume 34:Number 6(2022)
- Journal:
- International immunology
- Issue:
- Volume 34:Number 6(2022)
- Issue Display:
- Volume 34, Issue 6 (2022)
- Year:
- 2022
- Volume:
- 34
- Issue:
- 6
- Issue Sort Value:
- 2022-0034-0006-0000
- Page Start:
- 327
- Page End:
- 340
- Publication Date:
- 2022-03-16
- Subjects:
- bioinformatics -- exosome -- liquid biopsy -- omics -- precision medicine
Immunology -- Periodicals
616.079 - Journal URLs:
- http://intimm.oxfordjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/intimm/dxac009 ↗
- Languages:
- English
- ISSNs:
- 0953-8178
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4541.038930
British Library DSC - BLDSS-3PM
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- 21766.xml