To investigate the necessity of STRA6 upregulation in T cells during T cell immune responses.
Our earlier study revealed that STRA6 (stimulated by retinoic acid gene 6) was up-regulated within 3 h of TCR stimulation. STRA6 is the high-affinity receptor for plasma retinol-binding protein (RBP) and mediates cellular vitamin A uptake. We generated STRA6 knockout (KO) mice to assess whether such...
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doaj-03ce5f3f8a9e4c6d9375ac36068884652020-11-24T20:50:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01812e8280810.1371/journal.pone.0082808To investigate the necessity of STRA6 upregulation in T cells during T cell immune responses.Rafik TerraXuehai WangYan HuTania CharpentierAlain LamarreMing ZhongHui SunJianning MaoShijie QiHongyu LuoJiangping WuOur earlier study revealed that STRA6 (stimulated by retinoic acid gene 6) was up-regulated within 3 h of TCR stimulation. STRA6 is the high-affinity receptor for plasma retinol-binding protein (RBP) and mediates cellular vitamin A uptake. We generated STRA6 knockout (KO) mice to assess whether such up-regulation was critical for T-cell activation, differentiation and function. STRA6 KO mice under vitamin A sufficient conditions were fertile without apparent anomalies upon visual inspection. The size, cellularity and lymphocyte subpopulations of STRA6 KO thymus and spleen were comparable to those of their wild type (WT) controls. KO and WT T cells were similar in terms of TCR-stimulated proliferation in vitro and homeostatic expansion in vivo. Naive KO CD4 cells differentiated in vitro into Th1, Th2, Th17 as well as regulatory T cells in an analogous manner as their WT counterparts. In vivo experiments revealed that anti-viral immune responses to lymphocytic choriomeningitis virus in KO mice were comparable to those of WT controls. We also demonstrated that STRA6 KO and WT mice had similar glucose tolerance. Total vitamin A levels are dramatically lower in the eyes of KO mice as compared to those of WT mice, but the levels in other organs were not significantly affected after STRA6 deletion under vitamin A sufficient conditions, indicating that the eye is the mouse organ most sensitive to the loss of STRA6. Our results demonstrate that 1) in vitamin A sufficiency, the deletion of STRA6 in T cells does no affect the T-cell immune responses so-far tested, including those depend on STAT5 signaling; 2) STRA6-independent vitamin A uptake compensated the lack of STRA6 in lymphoid organs under vitamin A sufficient conditions in mice; 3) STRA6 is critical for vitamin A uptake in the eyes even in vitamin A sufficiency.http://europepmc.org/articles/PMC3876989?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Rafik Terra Xuehai Wang Yan Hu Tania Charpentier Alain Lamarre Ming Zhong Hui Sun Jianning Mao Shijie Qi Hongyu Luo Jiangping Wu |
spellingShingle |
Rafik Terra Xuehai Wang Yan Hu Tania Charpentier Alain Lamarre Ming Zhong Hui Sun Jianning Mao Shijie Qi Hongyu Luo Jiangping Wu To investigate the necessity of STRA6 upregulation in T cells during T cell immune responses. PLoS ONE |
author_facet |
Rafik Terra Xuehai Wang Yan Hu Tania Charpentier Alain Lamarre Ming Zhong Hui Sun Jianning Mao Shijie Qi Hongyu Luo Jiangping Wu |
author_sort |
Rafik Terra |
title |
To investigate the necessity of STRA6 upregulation in T cells during T cell immune responses. |
title_short |
To investigate the necessity of STRA6 upregulation in T cells during T cell immune responses. |
title_full |
To investigate the necessity of STRA6 upregulation in T cells during T cell immune responses. |
title_fullStr |
To investigate the necessity of STRA6 upregulation in T cells during T cell immune responses. |
title_full_unstemmed |
To investigate the necessity of STRA6 upregulation in T cells during T cell immune responses. |
title_sort |
to investigate the necessity of stra6 upregulation in t cells during t cell immune responses. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2013-01-01 |
description |
Our earlier study revealed that STRA6 (stimulated by retinoic acid gene 6) was up-regulated within 3 h of TCR stimulation. STRA6 is the high-affinity receptor for plasma retinol-binding protein (RBP) and mediates cellular vitamin A uptake. We generated STRA6 knockout (KO) mice to assess whether such up-regulation was critical for T-cell activation, differentiation and function. STRA6 KO mice under vitamin A sufficient conditions were fertile without apparent anomalies upon visual inspection. The size, cellularity and lymphocyte subpopulations of STRA6 KO thymus and spleen were comparable to those of their wild type (WT) controls. KO and WT T cells were similar in terms of TCR-stimulated proliferation in vitro and homeostatic expansion in vivo. Naive KO CD4 cells differentiated in vitro into Th1, Th2, Th17 as well as regulatory T cells in an analogous manner as their WT counterparts. In vivo experiments revealed that anti-viral immune responses to lymphocytic choriomeningitis virus in KO mice were comparable to those of WT controls. We also demonstrated that STRA6 KO and WT mice had similar glucose tolerance. Total vitamin A levels are dramatically lower in the eyes of KO mice as compared to those of WT mice, but the levels in other organs were not significantly affected after STRA6 deletion under vitamin A sufficient conditions, indicating that the eye is the mouse organ most sensitive to the loss of STRA6. Our results demonstrate that 1) in vitamin A sufficiency, the deletion of STRA6 in T cells does no affect the T-cell immune responses so-far tested, including those depend on STAT5 signaling; 2) STRA6-independent vitamin A uptake compensated the lack of STRA6 in lymphoid organs under vitamin A sufficient conditions in mice; 3) STRA6 is critical for vitamin A uptake in the eyes even in vitamin A sufficiency. |
url |
http://europepmc.org/articles/PMC3876989?pdf=render |
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