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Proteome analysis of the macroscopically affected colonic mucosa of Crohn’s disease and intestinal tuberculosis

Differentiation between intestinal tuberculosis (ITB) and Crohn’s disease (CD) is challenging in geographical regions where both these diseases are prevalent. There is a need of biomarkers for differentiation between these two disorders. Colonic biopsies from inflamed mucosa of treatment-naive patie...

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Autores principales: Rukmangadachar, Lokesh A., Makharia, Govind K., Mishra, Asha, Das, Prasenjit, Hariprasad, Gururao, Srinivasan, Alagiri, Gupta, Siddhartha Datta, Ahuja, Vineet, Acharya, Subrat K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4796817/
https://www.ncbi.nlm.nih.gov/pubmed/26988818
http://dx.doi.org/10.1038/srep23162
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author Rukmangadachar, Lokesh A.
Makharia, Govind K.
Mishra, Asha
Das, Prasenjit
Hariprasad, Gururao
Srinivasan, Alagiri
Gupta, Siddhartha Datta
Ahuja, Vineet
Acharya, Subrat K.
author_facet Rukmangadachar, Lokesh A.
Makharia, Govind K.
Mishra, Asha
Das, Prasenjit
Hariprasad, Gururao
Srinivasan, Alagiri
Gupta, Siddhartha Datta
Ahuja, Vineet
Acharya, Subrat K.
author_sort Rukmangadachar, Lokesh A.
collection PubMed
description Differentiation between intestinal tuberculosis (ITB) and Crohn’s disease (CD) is challenging in geographical regions where both these diseases are prevalent. There is a need of biomarkers for differentiation between these two disorders. Colonic biopsies from inflamed mucosa of treatment-naive patients with ITB, CD and controls were used for analysis. Protein extracted from biopsies was digested with trypsin and resulting peptides were labeled with iTRAQ reagents. The peptides were subsequently analyzed using LC-MS/MS for identification and quantification. Gene ontology annotation for proteins was analyzed in PANTHER. Validation experiments were done for six differentially expressed proteins using immunohistochemistry. 533 proteins were identified and 241 proteins were quantified from 5 sets of iTRAQ experiments. While 63 were differentially expressed in colonic mucosa of patients with CD and ITB in at least one set of iTRAQ experiment, 11 proteins were differentially expressed in more than one set of experiments. Six proteins used for validation using immunohistochemistry in a larger cohort of patients; none of them however was differentially expressed in patients with ITB and CD. There are differentially expressed proteins in tissue proteome of CD and ITB. Further experiments are required using a larger cohort of homogeneous tissue samples.
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spelling pubmed-47968172016-03-18 Proteome analysis of the macroscopically affected colonic mucosa of Crohn’s disease and intestinal tuberculosis Rukmangadachar, Lokesh A. Makharia, Govind K. Mishra, Asha Das, Prasenjit Hariprasad, Gururao Srinivasan, Alagiri Gupta, Siddhartha Datta Ahuja, Vineet Acharya, Subrat K. Sci Rep Article Differentiation between intestinal tuberculosis (ITB) and Crohn’s disease (CD) is challenging in geographical regions where both these diseases are prevalent. There is a need of biomarkers for differentiation between these two disorders. Colonic biopsies from inflamed mucosa of treatment-naive patients with ITB, CD and controls were used for analysis. Protein extracted from biopsies was digested with trypsin and resulting peptides were labeled with iTRAQ reagents. The peptides were subsequently analyzed using LC-MS/MS for identification and quantification. Gene ontology annotation for proteins was analyzed in PANTHER. Validation experiments were done for six differentially expressed proteins using immunohistochemistry. 533 proteins were identified and 241 proteins were quantified from 5 sets of iTRAQ experiments. While 63 were differentially expressed in colonic mucosa of patients with CD and ITB in at least one set of iTRAQ experiment, 11 proteins were differentially expressed in more than one set of experiments. Six proteins used for validation using immunohistochemistry in a larger cohort of patients; none of them however was differentially expressed in patients with ITB and CD. There are differentially expressed proteins in tissue proteome of CD and ITB. Further experiments are required using a larger cohort of homogeneous tissue samples. Nature Publishing Group 2016-03-18 /pmc/articles/PMC4796817/ /pubmed/26988818 http://dx.doi.org/10.1038/srep23162 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Rukmangadachar, Lokesh A.
Makharia, Govind K.
Mishra, Asha
Das, Prasenjit
Hariprasad, Gururao
Srinivasan, Alagiri
Gupta, Siddhartha Datta
Ahuja, Vineet
Acharya, Subrat K.
Proteome analysis of the macroscopically affected colonic mucosa of Crohn’s disease and intestinal tuberculosis
title Proteome analysis of the macroscopically affected colonic mucosa of Crohn’s disease and intestinal tuberculosis
title_full Proteome analysis of the macroscopically affected colonic mucosa of Crohn’s disease and intestinal tuberculosis
title_fullStr Proteome analysis of the macroscopically affected colonic mucosa of Crohn’s disease and intestinal tuberculosis
title_full_unstemmed Proteome analysis of the macroscopically affected colonic mucosa of Crohn’s disease and intestinal tuberculosis
title_short Proteome analysis of the macroscopically affected colonic mucosa of Crohn’s disease and intestinal tuberculosis
title_sort proteome analysis of the macroscopically affected colonic mucosa of crohn’s disease and intestinal tuberculosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4796817/
https://www.ncbi.nlm.nih.gov/pubmed/26988818
http://dx.doi.org/10.1038/srep23162
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