Proteomic profile of vitreous in patients with tubercular uveitis
To elucidate disease-specific host protein profile in vitreous fluid of patients with intraocular inflammation due to tubercular uveitis (TBU). Vitreous samples from 13 patients with TBU (group A), 7 with non-TBU (group B) and 9 with no uveitis (group C) were analysed by shotgun proteomics using Liq...
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Published in | Tuberculosis (Edinburgh, Scotland) Vol. 126; p. 102036 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Scotland
Elsevier Ltd
01.01.2021
Elsevier Science Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | To elucidate disease-specific host protein profile in vitreous fluid of patients with intraocular inflammation due to tubercular uveitis (TBU).
Vitreous samples from 13 patients with TBU (group A), 7 with non-TBU (group B) and 9 with no uveitis (group C) were analysed by shotgun proteomics using Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS). Differentially expressed proteins (DEPs) were subjected to pathway analysis using WEB-based Gene SeT Analysis Toolkit software.
Compared to control groups (B + C combined), group A (TBU) displayed 32 (11 upregulated, 21 downregulated) DEPs, which revealed an upregulation of coagulation cascades, complement and classic pathways, and downregulation of metabolism of carbohydrates, gluconeogenesis, glucose metabolism and glycolysis/gluconeogenesis pathways. When compared to group B (non-TBU) alone, TBU displayed 58 DEPs (21 upregulated, 37 downregulated), with an upregulation of apoptosis, KRAS signaling, diabetes pathways, classic pathways, and downregulation of MTORC1 signaling, glycolysis/gluconeogenesis, and glucose metabolism.
This differential protein profile provides novel insights into the molecular mechanisms of TBU and a baseline to explore vitreous biomarkers to differentiate TBU from non-TBU, warranting future studies to identify and validate them as a diagnostic tool in TBU. The enriched pathways generate interesting hypotheses and drive further research. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Present Address: Booz Allen Hamilton, McLean, VA, USA. IV: in charge of overall direction and planning, critical revision of the article. VG: sample collection, critical revision of the article. RB, MK, DRG: Designed and performed the experiments. Visiting Professor, University of Gdansk, Gdansk, Poland, EU SD: processed the experimental data, performed the analysis, supervised the manuscript and designed the figures and tables. AC: inputs in manuscript writing. Author contribution statement MK, NM, AN-L: sample processing, analysis and interpretation. MRD, JR: critical revision of the article. Both authors have contributed equally. All authors discussed the results and contributed to the final manuscript. SPS, AK, NS: experimental work. RB: Writing and editing of the manuscript, conducting the proteomics experiment, sample collection, literature search. AG: Conception or design of the work, sample collection, critical revision of the article, in charge of overall direction and planning, final approval of the version to be published SL: in charge of overall direction and planning. |
ISSN: | 1472-9792 1873-281X |
DOI: | 10.1016/j.tube.2020.102036 |