Ligand‐activated natural killer T lymphocytes promptly produce IL‐3 and GM‐CSF in vivo: relevance to peripheral myeloid recruitment
Natural killer (NK) T cells are prominent for their prompt IL‐4 and IFN‐γ production upon TCR ligation that enables them to influence acquired immune responses. In the present study we provide evidence that the regulatory functions of this particular T cell subset extend to the myeloid compartment o...
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Veröffentlicht in: | European journal of immunology 2002-07, Vol.32 (7), p.1897-1904 |
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container_title | European journal of immunology |
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creator | Leite‐de‐Moraes, Maria C. Lisbonne, Mariette Arnould, Anne Machavoine, François Herbelin, André Dy, Michel Schneider, Elke |
description | Natural killer (NK) T cells are prominent for their prompt IL‐4 and IFN‐γ production upon TCR ligation that enables them to influence acquired immune responses. In the present study we provide evidence that the regulatory functions of this particular T cell subset extend to the myeloid compartment of bone marrow and spleen through its production of hematopoietic growth factors. Bone marrow and spleen NKT cells responded to a single injection of their specific ligand α‐galactosylceramide (α‐GalCer) by producing both IL‐3 and granulocyte‐macrophage colony stimulating factor (GM‐CSF), whose colony‐stimulating activity became detectable in the serum as early as 1 h post treatment. These cytokines were not produced in mice lacking NKT cells (CD1d–/–), whose exclusive involvement in this biological activity was further confirmed by intracellular immuno‐staining. Growth factor production was accompanied by significant changes in the myeloid compartment of treated mice, namely mobilization of myeloid progenitors (colony‐forming unit cells, CFU‐C) and neutrophils from the bone marrow to the periphery. Taken together, our data support the notion that activated NKT cells influence innate immune responses by recruiting myeloid progenitors and granulocytes to the periphery through their production of hematopoietic growth factors. |
doi_str_mv | 10.1002/1521-4141(200207)32:7<1897::AID-IMMU1897>3.0.CO;2-Y |
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In the present study we provide evidence that the regulatory functions of this particular T cell subset extend to the myeloid compartment of bone marrow and spleen through its production of hematopoietic growth factors. Bone marrow and spleen NKT cells responded to a single injection of their specific ligand α‐galactosylceramide (α‐GalCer) by producing both IL‐3 and granulocyte‐macrophage colony stimulating factor (GM‐CSF), whose colony‐stimulating activity became detectable in the serum as early as 1 h post treatment. These cytokines were not produced in mice lacking NKT cells (CD1d–/–), whose exclusive involvement in this biological activity was further confirmed by intracellular immuno‐staining. Growth factor production was accompanied by significant changes in the myeloid compartment of treated mice, namely mobilization of myeloid progenitors (colony‐forming unit cells, CFU‐C) and neutrophils from the bone marrow to the periphery. 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In the present study we provide evidence that the regulatory functions of this particular T cell subset extend to the myeloid compartment of bone marrow and spleen through its production of hematopoietic growth factors. Bone marrow and spleen NKT cells responded to a single injection of their specific ligand α‐galactosylceramide (α‐GalCer) by producing both IL‐3 and granulocyte‐macrophage colony stimulating factor (GM‐CSF), whose colony‐stimulating activity became detectable in the serum as early as 1 h post treatment. These cytokines were not produced in mice lacking NKT cells (CD1d–/–), whose exclusive involvement in this biological activity was further confirmed by intracellular immuno‐staining. Growth factor production was accompanied by significant changes in the myeloid compartment of treated mice, namely mobilization of myeloid progenitors (colony‐forming unit cells, CFU‐C) and neutrophils from the bone marrow to the periphery. Taken together, our data support the notion that activated NKT cells influence innate immune responses by recruiting myeloid progenitors and granulocytes to the periphery through their production of hematopoietic growth factors.</description><subject>Animals</subject><subject>CD1d</subject><subject>Colony‐forming unit cell</subject><subject>Galactosylceramides - administration & dosage</subject><subject>Galactosylceramides - immunology</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - biosynthesis</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - genetics</subject><subject>Granulocytes - cytology</subject><subject>Granulocytes - immunology</subject><subject>Hematopoiesis, Extramedullary</subject><subject>Injections</subject><subject>Interferon-gamma - genetics</subject><subject>Interleukin-3 - biosynthesis</subject><subject>Interleukin-3 - genetics</subject><subject>Interleukin-4 - genetics</subject><subject>Killer Cells, Natural - drug effects</subject><subject>Killer Cells, Natural - immunology</subject><subject>Ligands</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Myeloid Cells - cytology</subject><subject>Myeloid Cells - immunology</subject><subject>Neutrophil</subject><subject>NKT lymphocyte</subject><subject>T-Lymphocytes - drug effects</subject><subject>T-Lymphocytes - immunology</subject><subject>α‐Galactosylceramide</subject><issn>0014-2980</issn><issn>1521-4141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkc9u1DAQxi0EokvhFZBPCA5ZxnYSJ9sKqUppWWlXe2gr0ZPlTSbU4PzBSbbKjSs3npEnwdEu5YQQJ8-Mv_k-2T9CThjMGQB_yyLOgpCF7DX3Lcg3gi_kKUtSuVicLc-D5Xp9M3XvxBzm2eaEB7ePyOxh6zGZAbAw4GkCR-RZ130GgDSO0qfkiHHGohjSGfm-Mp90Xfz89kPnvdnpHgta635w2tIvxlp09JrasWrvmnzssaOta6q2t-NUFEOOdLnyy4J6E3q59mV2dUFNTXdm1yyoQ4s7XXtZ39AWnWnvcLKuRrSNKfx97gbTV1j3z8mTUtsOXxzOY3Jz8f46-xCsNpfL7GwV5KFkMmBii3kpdBLHWoRCo5R5so2jCBIp44SD5pBKRORhGZaFEFsOZYQ5aIGyKFAck1d7X_-ArwN2vapMl6O1usZm6JT0fwpJxP8pZEkkI5aAF17thblrus5hqVpnKu1GxUBNKNUERU1Q1B6lElxJNcFTyqNUv1EqoUBlG8XVrXd9eYgfthUWfzwP7Lzg415wbyyO_5P5l8iHmfgFnoi9aA</recordid><startdate>200207</startdate><enddate>200207</enddate><creator>Leite‐de‐Moraes, Maria C.</creator><creator>Lisbonne, Mariette</creator><creator>Arnould, Anne</creator><creator>Machavoine, François</creator><creator>Herbelin, André</creator><creator>Dy, Michel</creator><creator>Schneider, Elke</creator><general>WILEY‐VCH Verlag GmbH</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200207</creationdate><title>Ligand‐activated natural killer T lymphocytes promptly produce IL‐3 and GM‐CSF in vivo: relevance to peripheral myeloid recruitment</title><author>Leite‐de‐Moraes, Maria C. ; 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In the present study we provide evidence that the regulatory functions of this particular T cell subset extend to the myeloid compartment of bone marrow and spleen through its production of hematopoietic growth factors. Bone marrow and spleen NKT cells responded to a single injection of their specific ligand α‐galactosylceramide (α‐GalCer) by producing both IL‐3 and granulocyte‐macrophage colony stimulating factor (GM‐CSF), whose colony‐stimulating activity became detectable in the serum as early as 1 h post treatment. These cytokines were not produced in mice lacking NKT cells (CD1d–/–), whose exclusive involvement in this biological activity was further confirmed by intracellular immuno‐staining. Growth factor production was accompanied by significant changes in the myeloid compartment of treated mice, namely mobilization of myeloid progenitors (colony‐forming unit cells, CFU‐C) and neutrophils from the bone marrow to the periphery. Taken together, our data support the notion that activated NKT cells influence innate immune responses by recruiting myeloid progenitors and granulocytes to the periphery through their production of hematopoietic growth factors.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH</pub><pmid>12115609</pmid><doi>10.1002/1521-4141(200207)32:7<1897::AID-IMMU1897>3.0.CO;2-Y</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals CD1d Colony‐forming unit cell Galactosylceramides - administration & dosage Galactosylceramides - immunology Granulocyte-Macrophage Colony-Stimulating Factor - biosynthesis Granulocyte-Macrophage Colony-Stimulating Factor - genetics Granulocytes - cytology Granulocytes - immunology Hematopoiesis, Extramedullary Injections Interferon-gamma - genetics Interleukin-3 - biosynthesis Interleukin-3 - genetics Interleukin-4 - genetics Killer Cells, Natural - drug effects Killer Cells, Natural - immunology Ligands Mice Mice, Inbred C57BL Mice, Knockout Myeloid Cells - cytology Myeloid Cells - immunology Neutrophil NKT lymphocyte T-Lymphocytes - drug effects T-Lymphocytes - immunology α‐Galactosylceramide |
title | Ligand‐activated natural killer T lymphocytes promptly produce IL‐3 and GM‐CSF in vivo: relevance to peripheral myeloid recruitment |
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