Semaphorin 3F and neuropilin-2 control the migration of human T-cell precursors.

Neuropilins and semaphorins are known as modulators of axon guidance, angiogenesis, and organogenesis in the developing nervous system, but have been recently evidenced as also playing a role in the immune system. Here we describe the expression and role of semaphorin 3F (SEMA3F) and its receptor ne...

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Autores principales: Daniella Arêas Mendes-da-Cruz, Anne Colette Brignier, Vahid Asnafi, Frederic Baleydier, Carolina Valença Messias, Yves Lepelletier, Nawel Bedjaoui, Amedée Renand, Salete Smaniotto, Danielle Canioni, Pierre Milpied, Karl Balabanian, Philippe Bousso, Stéphane Leprêtre, Yves Bertrand, Hervé Dombret, Norbert Ifrah, Mireille Dardenne, Elizabeth Macintyre, Wilson Savino, Olivier Hermine
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Publicado: Public Library of Science (PLoS) 2014
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Acceso en línea:https://doaj.org/article/e929d10fb6bf40a49a91edc2a5b6e629
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spelling oai:doaj.org-article:e929d10fb6bf40a49a91edc2a5b6e6292021-11-25T06:06:56ZSemaphorin 3F and neuropilin-2 control the migration of human T-cell precursors.1932-620310.1371/journal.pone.0103405https://doaj.org/article/e929d10fb6bf40a49a91edc2a5b6e6292014-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/25068647/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Neuropilins and semaphorins are known as modulators of axon guidance, angiogenesis, and organogenesis in the developing nervous system, but have been recently evidenced as also playing a role in the immune system. Here we describe the expression and role of semaphorin 3F (SEMA3F) and its receptor neuropilin-2 (NRP2) in human T cell precursors. NRP2 and SEMA3F are expressed in the human thymus, in both lymphoid and non-lymphoid compartments. SEMA3F have a repulsive effect on thymocyte migration and inhibited CXCL12- and sphingosine-1-phosphate (S1P)-induced thymocyte migration by inhibiting cytoskeleton reorganization prior to stimuli. Moreover, NRP2 and SEMA3F are expressed in human T-cell acute lymphoblastic leukemia/lymphoma primary cells. In these tumor cells, SEMA3F also blocks their migration induced by CXCL12 and S1P. Our data show that SEMA3F and NRP2 are further regulators of human thymocyte migration in physiological and pathological conditions.Daniella Arêas Mendes-da-CruzAnne Colette BrignierVahid AsnafiFrederic BaleydierCarolina Valença MessiasYves LepelletierNawel BedjaouiAmedée RenandSalete SmaniottoDanielle CanioniPierre MilpiedKarl BalabanianPhilippe BoussoStéphane LeprêtreYves BertrandHervé DombretNorbert IfrahMireille DardenneElizabeth MacintyreWilson SavinoOlivier HerminePublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 7, p e103405 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Daniella Arêas Mendes-da-Cruz
Anne Colette Brignier
Vahid Asnafi
Frederic Baleydier
Carolina Valença Messias
Yves Lepelletier
Nawel Bedjaoui
Amedée Renand
Salete Smaniotto
Danielle Canioni
Pierre Milpied
Karl Balabanian
Philippe Bousso
Stéphane Leprêtre
Yves Bertrand
Hervé Dombret
Norbert Ifrah
Mireille Dardenne
Elizabeth Macintyre
Wilson Savino
Olivier Hermine
Semaphorin 3F and neuropilin-2 control the migration of human T-cell precursors.
description Neuropilins and semaphorins are known as modulators of axon guidance, angiogenesis, and organogenesis in the developing nervous system, but have been recently evidenced as also playing a role in the immune system. Here we describe the expression and role of semaphorin 3F (SEMA3F) and its receptor neuropilin-2 (NRP2) in human T cell precursors. NRP2 and SEMA3F are expressed in the human thymus, in both lymphoid and non-lymphoid compartments. SEMA3F have a repulsive effect on thymocyte migration and inhibited CXCL12- and sphingosine-1-phosphate (S1P)-induced thymocyte migration by inhibiting cytoskeleton reorganization prior to stimuli. Moreover, NRP2 and SEMA3F are expressed in human T-cell acute lymphoblastic leukemia/lymphoma primary cells. In these tumor cells, SEMA3F also blocks their migration induced by CXCL12 and S1P. Our data show that SEMA3F and NRP2 are further regulators of human thymocyte migration in physiological and pathological conditions.
format article
author Daniella Arêas Mendes-da-Cruz
Anne Colette Brignier
Vahid Asnafi
Frederic Baleydier
Carolina Valença Messias
Yves Lepelletier
Nawel Bedjaoui
Amedée Renand
Salete Smaniotto
Danielle Canioni
Pierre Milpied
Karl Balabanian
Philippe Bousso
Stéphane Leprêtre
Yves Bertrand
Hervé Dombret
Norbert Ifrah
Mireille Dardenne
Elizabeth Macintyre
Wilson Savino
Olivier Hermine
author_facet Daniella Arêas Mendes-da-Cruz
Anne Colette Brignier
Vahid Asnafi
Frederic Baleydier
Carolina Valença Messias
Yves Lepelletier
Nawel Bedjaoui
Amedée Renand
Salete Smaniotto
Danielle Canioni
Pierre Milpied
Karl Balabanian
Philippe Bousso
Stéphane Leprêtre
Yves Bertrand
Hervé Dombret
Norbert Ifrah
Mireille Dardenne
Elizabeth Macintyre
Wilson Savino
Olivier Hermine
author_sort Daniella Arêas Mendes-da-Cruz
title Semaphorin 3F and neuropilin-2 control the migration of human T-cell precursors.
title_short Semaphorin 3F and neuropilin-2 control the migration of human T-cell precursors.
title_full Semaphorin 3F and neuropilin-2 control the migration of human T-cell precursors.
title_fullStr Semaphorin 3F and neuropilin-2 control the migration of human T-cell precursors.
title_full_unstemmed Semaphorin 3F and neuropilin-2 control the migration of human T-cell precursors.
title_sort semaphorin 3f and neuropilin-2 control the migration of human t-cell precursors.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/e929d10fb6bf40a49a91edc2a5b6e629
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