Selective reduction of post-selection CD8 thymocyte proliferation in IL-15Rα deficient mice.

Peripheral CD8(+) T cells are defective in both IL-15 and IL-15Rα knock-out (KO) mice; however, whether IL-15/IL-15Rα deficiency has a similar effect on CD8 single-positive (SP) thymocytes remains unclear. In this study, we investigated whether the absence of IL-15 transpresentation in IL-15Rα KO mi...

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Main Authors: Kai-Ping N Chow, Jian-Tai Qiu, Jam-Mou Lee, Shuo-Lun Hsu, Shan-Che Yang, Ning-Ning Wu, Wei Huang, Tzong-Shoon Wu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3308975?pdf=render
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author Kai-Ping N Chow
Jian-Tai Qiu
Jam-Mou Lee
Shuo-Lun Hsu
Shan-Che Yang
Ning-Ning Wu
Wei Huang
Tzong-Shoon Wu
author_facet Kai-Ping N Chow
Jian-Tai Qiu
Jam-Mou Lee
Shuo-Lun Hsu
Shan-Che Yang
Ning-Ning Wu
Wei Huang
Tzong-Shoon Wu
author_sort Kai-Ping N Chow
collection DOAJ
description Peripheral CD8(+) T cells are defective in both IL-15 and IL-15Rα knock-out (KO) mice; however, whether IL-15/IL-15Rα deficiency has a similar effect on CD8 single-positive (SP) thymocytes remains unclear. In this study, we investigated whether the absence of IL-15 transpresentation in IL-15Rα KO mice results in a defect in thymic CD8 single positive (SP) TCR(hi) thymocytes. Comparison of CD8SP TCR(hi) thymocytes from IL-15Rα KO mice with their wild type (WT) counterparts by flow cytometry showed a significant reduction in the percentage of CD69(-) CD8SP TCR(hi) thymocytes, which represent thymic premigrants. In addition, analysis of in vivo 5-bromo-2-deoxyuridine (BrdU) incorporation demonstrated that premigrant expansion of CD8SP TCR(hi) thymocytes was reduced in IL-15Rα KO mice. The presence of IL-15 transpresentation-dependent expansion in CD8SP TCR(hi) thymocytes was assessed by culturing total thymocytes in IL-15Rα-Fc fusion protein-pre-bound plates that were pre-incubated with IL-15 to mimic IL-15 transpresentation in vitro. The results demonstrated that CD8SP thymocytes selectively outgrew other thymic subsets. The contribution of the newly divided CD8SP thymocytes to the peripheral CD8(+) T cell pool was examined using double labeling with intrathymically injected FITC and intravenously injected BrdU. A marked decrease in FITC(+) BrdU(+) CD8(+) T cells was observed in the IL-15Rα KO lymph nodes. Through these experiments, we identified an IL-15 transpresentation-dependent proliferation process selective for the mature CD8SP premigrant subpopulation. Importantly, this process may contribute to the maintenance of the normal peripheral CD8(+) T cell pool.
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spelling doaj.art-d100bc280cb24ac0a79eae0b9ba11e762022-12-21T23:21:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0173e3315210.1371/journal.pone.0033152Selective reduction of post-selection CD8 thymocyte proliferation in IL-15Rα deficient mice.Kai-Ping N ChowJian-Tai QiuJam-Mou LeeShuo-Lun HsuShan-Che YangNing-Ning WuWei HuangTzong-Shoon WuPeripheral CD8(+) T cells are defective in both IL-15 and IL-15Rα knock-out (KO) mice; however, whether IL-15/IL-15Rα deficiency has a similar effect on CD8 single-positive (SP) thymocytes remains unclear. In this study, we investigated whether the absence of IL-15 transpresentation in IL-15Rα KO mice results in a defect in thymic CD8 single positive (SP) TCR(hi) thymocytes. Comparison of CD8SP TCR(hi) thymocytes from IL-15Rα KO mice with their wild type (WT) counterparts by flow cytometry showed a significant reduction in the percentage of CD69(-) CD8SP TCR(hi) thymocytes, which represent thymic premigrants. In addition, analysis of in vivo 5-bromo-2-deoxyuridine (BrdU) incorporation demonstrated that premigrant expansion of CD8SP TCR(hi) thymocytes was reduced in IL-15Rα KO mice. The presence of IL-15 transpresentation-dependent expansion in CD8SP TCR(hi) thymocytes was assessed by culturing total thymocytes in IL-15Rα-Fc fusion protein-pre-bound plates that were pre-incubated with IL-15 to mimic IL-15 transpresentation in vitro. The results demonstrated that CD8SP thymocytes selectively outgrew other thymic subsets. The contribution of the newly divided CD8SP thymocytes to the peripheral CD8(+) T cell pool was examined using double labeling with intrathymically injected FITC and intravenously injected BrdU. A marked decrease in FITC(+) BrdU(+) CD8(+) T cells was observed in the IL-15Rα KO lymph nodes. Through these experiments, we identified an IL-15 transpresentation-dependent proliferation process selective for the mature CD8SP premigrant subpopulation. Importantly, this process may contribute to the maintenance of the normal peripheral CD8(+) T cell pool.http://europepmc.org/articles/PMC3308975?pdf=render
spellingShingle Kai-Ping N Chow
Jian-Tai Qiu
Jam-Mou Lee
Shuo-Lun Hsu
Shan-Che Yang
Ning-Ning Wu
Wei Huang
Tzong-Shoon Wu
Selective reduction of post-selection CD8 thymocyte proliferation in IL-15Rα deficient mice.
PLoS ONE
title Selective reduction of post-selection CD8 thymocyte proliferation in IL-15Rα deficient mice.
title_full Selective reduction of post-selection CD8 thymocyte proliferation in IL-15Rα deficient mice.
title_fullStr Selective reduction of post-selection CD8 thymocyte proliferation in IL-15Rα deficient mice.
title_full_unstemmed Selective reduction of post-selection CD8 thymocyte proliferation in IL-15Rα deficient mice.
title_short Selective reduction of post-selection CD8 thymocyte proliferation in IL-15Rα deficient mice.
title_sort selective reduction of post selection cd8 thymocyte proliferation in il 15rα deficient mice
url http://europepmc.org/articles/PMC3308975?pdf=render
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