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Proteomic Analysis of Colonic Mucosal Tissue from Tuberculous and Ulcerative Colitis Patients
Changes in the expression profiles of specific proteins leads to serious human diseases, including colitis. The proteomic changes related to colitis and the differential expression between tuberculous (TC) and ulcerative colitis (UC) in colon tissue from colitis patients has not been defined. We the...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Physiological Society and The Korean Society of Pharmacology
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394922/ https://www.ncbi.nlm.nih.gov/pubmed/22802701 http://dx.doi.org/10.4196/kjpp.2012.16.3.193 |
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author | Kwon, Seong-Chun Won, Kyung Jong Jung, Seoung Hyo Lee, Kang Pa Lee, Dong-Youb Park, Eun-Seok Kim, Bokyung Cheon, Gab Jin Han, Koon Hee |
author_facet | Kwon, Seong-Chun Won, Kyung Jong Jung, Seoung Hyo Lee, Kang Pa Lee, Dong-Youb Park, Eun-Seok Kim, Bokyung Cheon, Gab Jin Han, Koon Hee |
author_sort | Kwon, Seong-Chun |
collection | PubMed |
description | Changes in the expression profiles of specific proteins leads to serious human diseases, including colitis. The proteomic changes related to colitis and the differential expression between tuberculous (TC) and ulcerative colitis (UC) in colon tissue from colitis patients has not been defined. We therefore performed a proteomic analysis of human TC and UC mucosal tissue. Total protein was obtained from the colon mucosal tissue of normal, TC, and UC patients, and resolved by 2-dimensional electrophoresis (2-DE). The results were analyzed with PDQuest using silver staining. We used matrix-assisted laser desorption ionization time-of-flight/time-of-flight spectrometry (MALDI TOF/TOF) to identify proteins differentially expressed in TC and UC. Of the over 1,000 proteins isolated, three in TC tissue and two in UC tissue displayed altered expression when compared to normal tissue. Moreover, two proteins were differentially expressed in a comparative analysis between TC and UC. These were identified as mutant β-actin, α-enolase and Charcot-Leyden crystal protein. In particular, the expression of α-enolase was significantly greater in TC compared with normal tissue, but decreased in comparison to UC, implying that α-enolase may represent a biomarker for differential diagnosis of TC and UC. This study therefore provides a valuable resource for the molecular and diagnostic analysis of human colitis. |
format | Online Article Text |
id | pubmed-3394922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Korean Physiological Society and The Korean Society of Pharmacology |
record_format | MEDLINE/PubMed |
spelling | pubmed-33949222012-07-16 Proteomic Analysis of Colonic Mucosal Tissue from Tuberculous and Ulcerative Colitis Patients Kwon, Seong-Chun Won, Kyung Jong Jung, Seoung Hyo Lee, Kang Pa Lee, Dong-Youb Park, Eun-Seok Kim, Bokyung Cheon, Gab Jin Han, Koon Hee Korean J Physiol Pharmacol Original Article Changes in the expression profiles of specific proteins leads to serious human diseases, including colitis. The proteomic changes related to colitis and the differential expression between tuberculous (TC) and ulcerative colitis (UC) in colon tissue from colitis patients has not been defined. We therefore performed a proteomic analysis of human TC and UC mucosal tissue. Total protein was obtained from the colon mucosal tissue of normal, TC, and UC patients, and resolved by 2-dimensional electrophoresis (2-DE). The results were analyzed with PDQuest using silver staining. We used matrix-assisted laser desorption ionization time-of-flight/time-of-flight spectrometry (MALDI TOF/TOF) to identify proteins differentially expressed in TC and UC. Of the over 1,000 proteins isolated, three in TC tissue and two in UC tissue displayed altered expression when compared to normal tissue. Moreover, two proteins were differentially expressed in a comparative analysis between TC and UC. These were identified as mutant β-actin, α-enolase and Charcot-Leyden crystal protein. In particular, the expression of α-enolase was significantly greater in TC compared with normal tissue, but decreased in comparison to UC, implying that α-enolase may represent a biomarker for differential diagnosis of TC and UC. This study therefore provides a valuable resource for the molecular and diagnostic analysis of human colitis. The Korean Physiological Society and The Korean Society of Pharmacology 2012-06 2012-06-26 /pmc/articles/PMC3394922/ /pubmed/22802701 http://dx.doi.org/10.4196/kjpp.2012.16.3.193 Text en Copyright © 2012 The Korean Physiological Society and The Korean Society of Pharmacology http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kwon, Seong-Chun Won, Kyung Jong Jung, Seoung Hyo Lee, Kang Pa Lee, Dong-Youb Park, Eun-Seok Kim, Bokyung Cheon, Gab Jin Han, Koon Hee Proteomic Analysis of Colonic Mucosal Tissue from Tuberculous and Ulcerative Colitis Patients |
title | Proteomic Analysis of Colonic Mucosal Tissue from Tuberculous and Ulcerative Colitis Patients |
title_full | Proteomic Analysis of Colonic Mucosal Tissue from Tuberculous and Ulcerative Colitis Patients |
title_fullStr | Proteomic Analysis of Colonic Mucosal Tissue from Tuberculous and Ulcerative Colitis Patients |
title_full_unstemmed | Proteomic Analysis of Colonic Mucosal Tissue from Tuberculous and Ulcerative Colitis Patients |
title_short | Proteomic Analysis of Colonic Mucosal Tissue from Tuberculous and Ulcerative Colitis Patients |
title_sort | proteomic analysis of colonic mucosal tissue from tuberculous and ulcerative colitis patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394922/ https://www.ncbi.nlm.nih.gov/pubmed/22802701 http://dx.doi.org/10.4196/kjpp.2012.16.3.193 |
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