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X-ray irradiation selectively kills thymocytes of different stages and impairs the maturation of donor-derived CD4(+)CD8(+) thymocytes in recipient thymus

The aim of the present study was to determine whether the sensitivity of thymocytes to X-ray radiation depends on their proliferative states and whether radiation impairs the maturation of donor-derived thymocytes in recipient thymus. We assigned 8-week-old C57BL/6J mice into three treatment groups:...

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Autores principales: Li, Jinbo, Cai, Hongquan, Jin, Jianliang, Wang, Qian, Miao, Dengshun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Department of Journal of Biomedical Research 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613732/
https://www.ncbi.nlm.nih.gov/pubmed/23554771
http://dx.doi.org/10.7555/JBR.26.20120003
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author Li, Jinbo
Cai, Hongquan
Jin, Jianliang
Wang, Qian
Miao, Dengshun
author_facet Li, Jinbo
Cai, Hongquan
Jin, Jianliang
Wang, Qian
Miao, Dengshun
author_sort Li, Jinbo
collection PubMed
description The aim of the present study was to determine whether the sensitivity of thymocytes to X-ray radiation depends on their proliferative states and whether radiation impairs the maturation of donor-derived thymocytes in recipient thymus. We assigned 8-week-old C57BL/6J mice into three treatment groups: 1) untreated; 2) X-ray radiation; 3) X-ray radiation plus bone marrow transplantation with donor bone marrow cells from transgenic mice expressing enhanced green fluorescent protein (GFP) on a universal promoter. After 4 weeks, the size of the thymus, the number and proliferation of thymocytes and ratios of different stage thymocytes were analyzed by immunohistochemistry and flow cytometry. The results showed that: 1) CD4(+)CD8(+) thymocytes were more sensitive to X-ray radiation-induced cell death than other thymocytes; 2) the proliferative capacity of CD4(+)CD8(+) thymocytes was higher than that of other thymocytes; 3) the size of the thymus, the number of thymocytes and ratios of thymocytes of different stages in irradiated mice recovered to the normal level of untreated mice by bone marrow transplantation; 4) the ratio of GFP-positive CD4(+)CD8(+) thymocytes increased significantly, whereas the ratio of GFP-positive CD4(+) or CD8(+) thymocytes decreased significantly. These results indicate that the degree of sensitivity of thymocytes to X-ray radiation depends on their proliferative states and radiation impairs the maturation of donor-derived CD4(+)CD8(+) thymocytes in recipient thymus.
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spelling pubmed-36137322013-04-02 X-ray irradiation selectively kills thymocytes of different stages and impairs the maturation of donor-derived CD4(+)CD8(+) thymocytes in recipient thymus Li, Jinbo Cai, Hongquan Jin, Jianliang Wang, Qian Miao, Dengshun J Biomed Res Research Paper The aim of the present study was to determine whether the sensitivity of thymocytes to X-ray radiation depends on their proliferative states and whether radiation impairs the maturation of donor-derived thymocytes in recipient thymus. We assigned 8-week-old C57BL/6J mice into three treatment groups: 1) untreated; 2) X-ray radiation; 3) X-ray radiation plus bone marrow transplantation with donor bone marrow cells from transgenic mice expressing enhanced green fluorescent protein (GFP) on a universal promoter. After 4 weeks, the size of the thymus, the number and proliferation of thymocytes and ratios of different stage thymocytes were analyzed by immunohistochemistry and flow cytometry. The results showed that: 1) CD4(+)CD8(+) thymocytes were more sensitive to X-ray radiation-induced cell death than other thymocytes; 2) the proliferative capacity of CD4(+)CD8(+) thymocytes was higher than that of other thymocytes; 3) the size of the thymus, the number of thymocytes and ratios of thymocytes of different stages in irradiated mice recovered to the normal level of untreated mice by bone marrow transplantation; 4) the ratio of GFP-positive CD4(+)CD8(+) thymocytes increased significantly, whereas the ratio of GFP-positive CD4(+) or CD8(+) thymocytes decreased significantly. These results indicate that the degree of sensitivity of thymocytes to X-ray radiation depends on their proliferative states and radiation impairs the maturation of donor-derived CD4(+)CD8(+) thymocytes in recipient thymus. Editorial Department of Journal of Biomedical Research 2012-09 2012-06-08 /pmc/articles/PMC3613732/ /pubmed/23554771 http://dx.doi.org/10.7555/JBR.26.20120003 Text en © 2012 by the Journal of Biomedical Research. All rights reserved. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Research Paper
Li, Jinbo
Cai, Hongquan
Jin, Jianliang
Wang, Qian
Miao, Dengshun
X-ray irradiation selectively kills thymocytes of different stages and impairs the maturation of donor-derived CD4(+)CD8(+) thymocytes in recipient thymus
title X-ray irradiation selectively kills thymocytes of different stages and impairs the maturation of donor-derived CD4(+)CD8(+) thymocytes in recipient thymus
title_full X-ray irradiation selectively kills thymocytes of different stages and impairs the maturation of donor-derived CD4(+)CD8(+) thymocytes in recipient thymus
title_fullStr X-ray irradiation selectively kills thymocytes of different stages and impairs the maturation of donor-derived CD4(+)CD8(+) thymocytes in recipient thymus
title_full_unstemmed X-ray irradiation selectively kills thymocytes of different stages and impairs the maturation of donor-derived CD4(+)CD8(+) thymocytes in recipient thymus
title_short X-ray irradiation selectively kills thymocytes of different stages and impairs the maturation of donor-derived CD4(+)CD8(+) thymocytes in recipient thymus
title_sort x-ray irradiation selectively kills thymocytes of different stages and impairs the maturation of donor-derived cd4(+)cd8(+) thymocytes in recipient thymus
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613732/
https://www.ncbi.nlm.nih.gov/pubmed/23554771
http://dx.doi.org/10.7555/JBR.26.20120003
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