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Early Detection of T cell Transfer-induced Autoimmune Colitis by In Vivo Imaging System
Inflammatory bowel disease is a chronic and progressive inflammatory intestinal disease that includes two major types, namely ulcerative colitis and Crohn’s disease (CD). CD is characterized by intestinal epithelial hyperplasia and inflammatory cell infiltration. Transfer of CD25(−)CD45RB(hi)CD4(+)...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071899/ https://www.ncbi.nlm.nih.gov/pubmed/27762297 http://dx.doi.org/10.1038/srep35635 |
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author | Chen, Yu-Ling Chen, Yi-Ting Lo, Cheng-Feng Hsieh, Ching-I Chiu, Shang-Yi Wu, Chang-Yen Yeh, Yu-Shan Hung, Shu-Hsuan Cheng, Po-Hao Su, Yu-Hsuan Jiang, Si-Tse Chin, Hsian-Jean Su, Yu-Chia |
author_facet | Chen, Yu-Ling Chen, Yi-Ting Lo, Cheng-Feng Hsieh, Ching-I Chiu, Shang-Yi Wu, Chang-Yen Yeh, Yu-Shan Hung, Shu-Hsuan Cheng, Po-Hao Su, Yu-Hsuan Jiang, Si-Tse Chin, Hsian-Jean Su, Yu-Chia |
author_sort | Chen, Yu-Ling |
collection | PubMed |
description | Inflammatory bowel disease is a chronic and progressive inflammatory intestinal disease that includes two major types, namely ulcerative colitis and Crohn’s disease (CD). CD is characterized by intestinal epithelial hyperplasia and inflammatory cell infiltration. Transfer of CD25(−)CD45RB(hi)CD4(+) (naïve) T cells into immunodeficiency mice induces autoimmune colitis with pathological lesions similar to CD and loss of body weight 4 weeks after cell transfer. However, weight loss neither has sufficient sensitivity nor totally matches the pathological findings of CD. To establish an early and sensitive indicator of autoimmune colitis model, the transferred T cell-induced colitis mouse model was modified by transferring luciferase-expressing donor T cells and determining the colitis by in vivo imaging system (IVIS). Colitis was detected with IVIS 7–10 days before the onset of body weight loss and diarrhea. IVIS was also applied in the dexamethasone treatment trial, and was a more sensitive indicator than body weight changes. All IVIS signals were parallel to the pathological abnormalities of the gut and immunological analysis results. In summary, IVIS provides both sensitive and objective means to monitor the disease course of transferred T cell-induced CD and fulfills the 3Rs principle of humane care of laboratory animals. |
format | Online Article Text |
id | pubmed-5071899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50718992016-10-26 Early Detection of T cell Transfer-induced Autoimmune Colitis by In Vivo Imaging System Chen, Yu-Ling Chen, Yi-Ting Lo, Cheng-Feng Hsieh, Ching-I Chiu, Shang-Yi Wu, Chang-Yen Yeh, Yu-Shan Hung, Shu-Hsuan Cheng, Po-Hao Su, Yu-Hsuan Jiang, Si-Tse Chin, Hsian-Jean Su, Yu-Chia Sci Rep Article Inflammatory bowel disease is a chronic and progressive inflammatory intestinal disease that includes two major types, namely ulcerative colitis and Crohn’s disease (CD). CD is characterized by intestinal epithelial hyperplasia and inflammatory cell infiltration. Transfer of CD25(−)CD45RB(hi)CD4(+) (naïve) T cells into immunodeficiency mice induces autoimmune colitis with pathological lesions similar to CD and loss of body weight 4 weeks after cell transfer. However, weight loss neither has sufficient sensitivity nor totally matches the pathological findings of CD. To establish an early and sensitive indicator of autoimmune colitis model, the transferred T cell-induced colitis mouse model was modified by transferring luciferase-expressing donor T cells and determining the colitis by in vivo imaging system (IVIS). Colitis was detected with IVIS 7–10 days before the onset of body weight loss and diarrhea. IVIS was also applied in the dexamethasone treatment trial, and was a more sensitive indicator than body weight changes. All IVIS signals were parallel to the pathological abnormalities of the gut and immunological analysis results. In summary, IVIS provides both sensitive and objective means to monitor the disease course of transferred T cell-induced CD and fulfills the 3Rs principle of humane care of laboratory animals. Nature Publishing Group 2016-10-20 /pmc/articles/PMC5071899/ /pubmed/27762297 http://dx.doi.org/10.1038/srep35635 Text en Copyright © 2016, The Author(s) 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 Chen, Yu-Ling Chen, Yi-Ting Lo, Cheng-Feng Hsieh, Ching-I Chiu, Shang-Yi Wu, Chang-Yen Yeh, Yu-Shan Hung, Shu-Hsuan Cheng, Po-Hao Su, Yu-Hsuan Jiang, Si-Tse Chin, Hsian-Jean Su, Yu-Chia Early Detection of T cell Transfer-induced Autoimmune Colitis by In Vivo Imaging System |
title | Early Detection of T cell Transfer-induced Autoimmune Colitis by In Vivo Imaging System |
title_full | Early Detection of T cell Transfer-induced Autoimmune Colitis by In Vivo Imaging System |
title_fullStr | Early Detection of T cell Transfer-induced Autoimmune Colitis by In Vivo Imaging System |
title_full_unstemmed | Early Detection of T cell Transfer-induced Autoimmune Colitis by In Vivo Imaging System |
title_short | Early Detection of T cell Transfer-induced Autoimmune Colitis by In Vivo Imaging System |
title_sort | early detection of t cell transfer-induced autoimmune colitis by in vivo imaging system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5071899/ https://www.ncbi.nlm.nih.gov/pubmed/27762297 http://dx.doi.org/10.1038/srep35635 |
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