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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Main Authors: Rafik Terra, Xuehai Wang, Yan Hu, Tania Charpentier, Alain Lamarre, Ming Zhong, Hui Sun, Jianning Mao, Shijie Qi, Hongyu Luo, Jiangping Wu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3876989?pdf=render
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spelling 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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