author_facet Azevedo, Rita I.
Soares, Maria Vieira D.
Barata, João T.
Tendeiro, Rita
Serra-Caetano, Ana
Victorino, Rui M. M.
Sousa, Ana E.
Azevedo, Rita I.
Soares, Maria Vieira D.
Barata, João T.
Tendeiro, Rita
Serra-Caetano, Ana
Victorino, Rui M. M.
Sousa, Ana E.
author Azevedo, Rita I.
Soares, Maria Vieira D.
Barata, João T.
Tendeiro, Rita
Serra-Caetano, Ana
Victorino, Rui M. M.
Sousa, Ana E.
spellingShingle Azevedo, Rita I.
Soares, Maria Vieira D.
Barata, João T.
Tendeiro, Rita
Serra-Caetano, Ana
Victorino, Rui M. M.
Sousa, Ana E.
Blood
IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
Cell Biology
Hematology
Immunology
Biochemistry
author_sort azevedo, rita i.
spelling Azevedo, Rita I. Soares, Maria Vieira D. Barata, João T. Tendeiro, Rita Serra-Caetano, Ana Victorino, Rui M. M. Sousa, Ana E. 0006-4971 1528-0020 American Society of Hematology Cell Biology Hematology Immunology Biochemistry http://dx.doi.org/10.1182/blood-2008-07-166223 <jats:title>Abstract</jats:title><jats:p>The CD31+ subset of human naive CD4+ T cells is thought to contain the population of cells that have recently emigrated from the thymus, while their CD31− counterparts have been proposed to originate from CD31+ cells after homeostatic cell division. Naive T-cell maintenance is known to involve homeostatic cytokines such as interleukin-7 (IL-7). It remains to be investigated what role this cytokine has in the homeostasis of naive CD4+ T-cell subsets defined by CD31 expression. We provide evidence that IL-7 exerts a preferential proliferative effect on CD31+ naive CD4+ T cells from adult peripheral blood compared with the CD31− subset. IL-7–driven proliferation did not result in loss of CD31 expression, suggesting that CD31+ naive CD4+ T cells can undergo cytokine-driven homeostatic proliferation while preserving CD31. Furthermore, IL-7 sustained or increased CD31 expression even in nonproliferating cells. Both proliferation and CD31 maintenance were dependent on the activation of phosphoinositide 3-kinase (PI3K) signaling. Taken together, our data suggest that during adulthood CD31+ naive CD4+ T cells are maintained by IL-7 and that IL-7–based therapies may exert a preferential effect on this population.</jats:p> IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner Blood
doi_str_mv 10.1182/blood-2008-07-166223
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source_id 49
title IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
title_unstemmed IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
title_full IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
title_fullStr IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
title_full_unstemmed IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
title_short IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
title_sort il-7 sustains cd31 expression in human naive cd4+ t cells and preferentially expands the cd31+ subset in a pi3k-dependent manner
topic Cell Biology
Hematology
Immunology
Biochemistry
url http://dx.doi.org/10.1182/blood-2008-07-166223
publishDate 2009
physical 2999-3007
description <jats:title>Abstract</jats:title><jats:p>The CD31+ subset of human naive CD4+ T cells is thought to contain the population of cells that have recently emigrated from the thymus, while their CD31− counterparts have been proposed to originate from CD31+ cells after homeostatic cell division. Naive T-cell maintenance is known to involve homeostatic cytokines such as interleukin-7 (IL-7). It remains to be investigated what role this cytokine has in the homeostasis of naive CD4+ T-cell subsets defined by CD31 expression. We provide evidence that IL-7 exerts a preferential proliferative effect on CD31+ naive CD4+ T cells from adult peripheral blood compared with the CD31− subset. IL-7–driven proliferation did not result in loss of CD31 expression, suggesting that CD31+ naive CD4+ T cells can undergo cytokine-driven homeostatic proliferation while preserving CD31. Furthermore, IL-7 sustained or increased CD31 expression even in nonproliferating cells. Both proliferation and CD31 maintenance were dependent on the activation of phosphoinositide 3-kinase (PI3K) signaling. Taken together, our data suggest that during adulthood CD31+ naive CD4+ T cells are maintained by IL-7 and that IL-7–based therapies may exert a preferential effect on this population.</jats:p>
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author Azevedo, Rita I., Soares, Maria Vieira D., Barata, João T., Tendeiro, Rita, Serra-Caetano, Ana, Victorino, Rui M. M., Sousa, Ana E.
author_facet Azevedo, Rita I., Soares, Maria Vieira D., Barata, João T., Tendeiro, Rita, Serra-Caetano, Ana, Victorino, Rui M. M., Sousa, Ana E., Azevedo, Rita I., Soares, Maria Vieira D., Barata, João T., Tendeiro, Rita, Serra-Caetano, Ana, Victorino, Rui M. M., Sousa, Ana E.
author_sort azevedo, rita i.
container_issue 13
container_start_page 2999
container_title Blood
container_volume 113
description <jats:title>Abstract</jats:title><jats:p>The CD31+ subset of human naive CD4+ T cells is thought to contain the population of cells that have recently emigrated from the thymus, while their CD31− counterparts have been proposed to originate from CD31+ cells after homeostatic cell division. Naive T-cell maintenance is known to involve homeostatic cytokines such as interleukin-7 (IL-7). It remains to be investigated what role this cytokine has in the homeostasis of naive CD4+ T-cell subsets defined by CD31 expression. We provide evidence that IL-7 exerts a preferential proliferative effect on CD31+ naive CD4+ T cells from adult peripheral blood compared with the CD31− subset. IL-7–driven proliferation did not result in loss of CD31 expression, suggesting that CD31+ naive CD4+ T cells can undergo cytokine-driven homeostatic proliferation while preserving CD31. Furthermore, IL-7 sustained or increased CD31 expression even in nonproliferating cells. Both proliferation and CD31 maintenance were dependent on the activation of phosphoinositide 3-kinase (PI3K) signaling. Taken together, our data suggest that during adulthood CD31+ naive CD4+ T cells are maintained by IL-7 and that IL-7–based therapies may exert a preferential effect on this population.</jats:p>
doi_str_mv 10.1182/blood-2008-07-166223
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imprint American Society of Hematology, 2009
imprint_str_mv American Society of Hematology, 2009
institution DE-D275, DE-Bn3, DE-Brt1, DE-Zwi2, DE-D161, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229
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spelling Azevedo, Rita I. Soares, Maria Vieira D. Barata, João T. Tendeiro, Rita Serra-Caetano, Ana Victorino, Rui M. M. Sousa, Ana E. 0006-4971 1528-0020 American Society of Hematology Cell Biology Hematology Immunology Biochemistry http://dx.doi.org/10.1182/blood-2008-07-166223 <jats:title>Abstract</jats:title><jats:p>The CD31+ subset of human naive CD4+ T cells is thought to contain the population of cells that have recently emigrated from the thymus, while their CD31− counterparts have been proposed to originate from CD31+ cells after homeostatic cell division. Naive T-cell maintenance is known to involve homeostatic cytokines such as interleukin-7 (IL-7). It remains to be investigated what role this cytokine has in the homeostasis of naive CD4+ T-cell subsets defined by CD31 expression. We provide evidence that IL-7 exerts a preferential proliferative effect on CD31+ naive CD4+ T cells from adult peripheral blood compared with the CD31− subset. IL-7–driven proliferation did not result in loss of CD31 expression, suggesting that CD31+ naive CD4+ T cells can undergo cytokine-driven homeostatic proliferation while preserving CD31. Furthermore, IL-7 sustained or increased CD31 expression even in nonproliferating cells. Both proliferation and CD31 maintenance were dependent on the activation of phosphoinositide 3-kinase (PI3K) signaling. Taken together, our data suggest that during adulthood CD31+ naive CD4+ T cells are maintained by IL-7 and that IL-7–based therapies may exert a preferential effect on this population.</jats:p> IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner Blood
spellingShingle Azevedo, Rita I., Soares, Maria Vieira D., Barata, João T., Tendeiro, Rita, Serra-Caetano, Ana, Victorino, Rui M. M., Sousa, Ana E., Blood, IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner, Cell Biology, Hematology, Immunology, Biochemistry
title IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
title_full IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
title_fullStr IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
title_full_unstemmed IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
title_short IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
title_sort il-7 sustains cd31 expression in human naive cd4+ t cells and preferentially expands the cd31+ subset in a pi3k-dependent manner
title_unstemmed IL-7 sustains CD31 expression in human naive CD4+ T cells and preferentially expands the CD31+ subset in a PI3K-dependent manner
topic Cell Biology, Hematology, Immunology, Biochemistry
url http://dx.doi.org/10.1182/blood-2008-07-166223