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Disturbances in apoptosis of lamina propria lymphocytes in Crohn's disease
INTRODUCTION: The aim of this study was to assess the potential mechanisms providing resistance to apoptosis of lamina propria lymphocytes (LPL) directlyin intestinal tissues from patients with Crohn's disease (CD). MATERIAL AND METHODS: Fifty CD patients were enrolled in the study. The control...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4697047/ https://www.ncbi.nlm.nih.gov/pubmed/26788091 http://dx.doi.org/10.5114/aoms.2015.54203 |
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author | Eder, Piotr Łykowska-Szuber, Liliana Krela-Kaźmierczak, Iwona Stawczyk-Eder, Kamila Iwanik, Katarzyna Majewski, Przemysław Sterzyńska, Karolina Zabel, Maciej Linke, Krzysztof |
author_facet | Eder, Piotr Łykowska-Szuber, Liliana Krela-Kaźmierczak, Iwona Stawczyk-Eder, Kamila Iwanik, Katarzyna Majewski, Przemysław Sterzyńska, Karolina Zabel, Maciej Linke, Krzysztof |
author_sort | Eder, Piotr |
collection | PubMed |
description | INTRODUCTION: The aim of this study was to assess the potential mechanisms providing resistance to apoptosis of lamina propria lymphocytes (LPL) directlyin intestinal tissues from patients with Crohn's disease (CD). MATERIAL AND METHODS: Fifty CD patients were enrolled in the study. The control group consisted of healthy patients who underwent surveillance colonoscopy after endoscopic polypectomy. Each CD patient underwent colonoscopy with tissue sampling from inflamed areas of the colon with the assessment of immunohistochemical expression of active caspase 3, Fas, tumour necrosis factor receptor 1 (TNFR1), Bcl-2, Bax, CD4 and CD8. This was compared with healthy intestinal mucosa. RESULTS: The expression of active caspase 3 was significantly lower in LPL in CD (0.4 ±0.3 vs. 2.8 ±1.5; p = 0.0002). A statistically significant increase of CD4 and CD8 positive cells was noted in CD (2.3 ±0.5 vs. 1.2 ±0.2, p < 0.0001; 2.1 ±0.3 vs. 1.1 ±0.3, p < 0.0001, respectively). It was associated with a significant increase of the Bcl-2 (6.7 ±2.7 vs. 2.9 ±0.8; p < 0.0001) and a decrease of the Bax protein expression (3.4 ±2.1 vs. 5.5 ±1.8; p < 0.0001) in CD. The expression of Fas and TNFR1 did not differ between the study groups. CONCLUSIONS: LPL in CD are resistant to apoptosis when compared with physiological conditions. This is probably due to an imbalance in Bcl-2 family proteins. TNFR1-related pathway is probably not involved in disturbances of LPL apoptosis in CD. |
format | Online Article Text |
id | pubmed-4697047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-46970472016-01-19 Disturbances in apoptosis of lamina propria lymphocytes in Crohn's disease Eder, Piotr Łykowska-Szuber, Liliana Krela-Kaźmierczak, Iwona Stawczyk-Eder, Kamila Iwanik, Katarzyna Majewski, Przemysław Sterzyńska, Karolina Zabel, Maciej Linke, Krzysztof Arch Med Sci Basic Research INTRODUCTION: The aim of this study was to assess the potential mechanisms providing resistance to apoptosis of lamina propria lymphocytes (LPL) directlyin intestinal tissues from patients with Crohn's disease (CD). MATERIAL AND METHODS: Fifty CD patients were enrolled in the study. The control group consisted of healthy patients who underwent surveillance colonoscopy after endoscopic polypectomy. Each CD patient underwent colonoscopy with tissue sampling from inflamed areas of the colon with the assessment of immunohistochemical expression of active caspase 3, Fas, tumour necrosis factor receptor 1 (TNFR1), Bcl-2, Bax, CD4 and CD8. This was compared with healthy intestinal mucosa. RESULTS: The expression of active caspase 3 was significantly lower in LPL in CD (0.4 ±0.3 vs. 2.8 ±1.5; p = 0.0002). A statistically significant increase of CD4 and CD8 positive cells was noted in CD (2.3 ±0.5 vs. 1.2 ±0.2, p < 0.0001; 2.1 ±0.3 vs. 1.1 ±0.3, p < 0.0001, respectively). It was associated with a significant increase of the Bcl-2 (6.7 ±2.7 vs. 2.9 ±0.8; p < 0.0001) and a decrease of the Bax protein expression (3.4 ±2.1 vs. 5.5 ±1.8; p < 0.0001) in CD. The expression of Fas and TNFR1 did not differ between the study groups. CONCLUSIONS: LPL in CD are resistant to apoptosis when compared with physiological conditions. This is probably due to an imbalance in Bcl-2 family proteins. TNFR1-related pathway is probably not involved in disturbances of LPL apoptosis in CD. Termedia Publishing House 2015-12-11 2015-12-10 /pmc/articles/PMC4697047/ /pubmed/26788091 http://dx.doi.org/10.5114/aoms.2015.54203 Text en Copyright © 2015 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Basic Research Eder, Piotr Łykowska-Szuber, Liliana Krela-Kaźmierczak, Iwona Stawczyk-Eder, Kamila Iwanik, Katarzyna Majewski, Przemysław Sterzyńska, Karolina Zabel, Maciej Linke, Krzysztof Disturbances in apoptosis of lamina propria lymphocytes in Crohn's disease |
title | Disturbances in apoptosis of lamina propria lymphocytes in Crohn's disease |
title_full | Disturbances in apoptosis of lamina propria lymphocytes in Crohn's disease |
title_fullStr | Disturbances in apoptosis of lamina propria lymphocytes in Crohn's disease |
title_full_unstemmed | Disturbances in apoptosis of lamina propria lymphocytes in Crohn's disease |
title_short | Disturbances in apoptosis of lamina propria lymphocytes in Crohn's disease |
title_sort | disturbances in apoptosis of lamina propria lymphocytes in crohn's disease |
topic | Basic Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4697047/ https://www.ncbi.nlm.nih.gov/pubmed/26788091 http://dx.doi.org/10.5114/aoms.2015.54203 |
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