Differentiation of hematopoietic stem cell and myeloid populations by ATP is modulated by cytokines
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
dARK ID: | ark:/48912/00130000174dm |
Texto Completo: | https://dx.doi.org/10.1038/cddis.2011.49 https://repositorio.unifesp.br/handle/11600/33721 |
Resumo: | Extracellular nucleotides are emerging as important regulators of inflammation, cell proliferation and differentiation in a variety of tissues, including the hematopoietic system. in this study, the role of ATP was investigated during murine hematopoiesis. ATP was able to reduce the percentage of hematopoietic stem cells (HSCs), common myeloid progenitors and granulocyte-macrophage progenitors (GMPs), whereas differentiation into megakaryocyte-erythroid progenitors was not affected. in addition, in vivo administration of ATP to mice reduced the number of GMPs, but increased the number of Gr-1(+)Mac-1(+) myeloid cells. ATP also induced an increased proliferation rate and reduced Notch expression in HSCs and impaired HSC-mediated bone marrow reconstitution in sublethally irradiated mice. Moreover, the effects elicited by ATP were inhibited by suramin, a P2 receptor antagonist, and BAPTA, an intracellular Ca(2+) chelator. We further investigated whether the presence of cytokines might modulate the observed ATP-induced differentiation. Treatment of cells with cytokines (stem cell factor, interleukin-3 and granulocyte-monocyte colony stimulator factor) before ATP stimulation led to reduced ATP-dependent differentiation in long-term bone marrow cultures, thereby restoring the ability of HSCs to reconstitute hematopoiesis. Thus, our data suggest that ATP induces the differentiation of murine HSCs into the myeloid lineage and that this effect can be modulated by cytokines. Cell Death and Disease (2011) 2, e165; doi:10.1038/cddis.2011.49; published online 2 June 2011 |
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Differentiation of hematopoietic stem cell and myeloid populations by ATP is modulated by cytokinesATPP2 receptorsHematopoietic stem cellDifferentiationMyeloidCytokinesExtracellular nucleotides are emerging as important regulators of inflammation, cell proliferation and differentiation in a variety of tissues, including the hematopoietic system. in this study, the role of ATP was investigated during murine hematopoiesis. ATP was able to reduce the percentage of hematopoietic stem cells (HSCs), common myeloid progenitors and granulocyte-macrophage progenitors (GMPs), whereas differentiation into megakaryocyte-erythroid progenitors was not affected. in addition, in vivo administration of ATP to mice reduced the number of GMPs, but increased the number of Gr-1(+)Mac-1(+) myeloid cells. ATP also induced an increased proliferation rate and reduced Notch expression in HSCs and impaired HSC-mediated bone marrow reconstitution in sublethally irradiated mice. Moreover, the effects elicited by ATP were inhibited by suramin, a P2 receptor antagonist, and BAPTA, an intracellular Ca(2+) chelator. We further investigated whether the presence of cytokines might modulate the observed ATP-induced differentiation. Treatment of cells with cytokines (stem cell factor, interleukin-3 and granulocyte-monocyte colony stimulator factor) before ATP stimulation led to reduced ATP-dependent differentiation in long-term bone marrow cultures, thereby restoring the ability of HSCs to reconstitute hematopoiesis. Thus, our data suggest that ATP induces the differentiation of murine HSCs into the myeloid lineage and that this effect can be modulated by cytokines. Cell Death and Disease (2011) 2, e165; doi:10.1038/cddis.2011.49; published online 2 June 2011Universidade Federal de São Paulo, Dept Biofis, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biofis, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Bioquim, BR-04044020 São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)FAPESP: 2007/58589-9Nature Publishing GroupUniversidade Federal de São Paulo (UNIFESP)Barbosa, Christiano Marcello Vaz [UNIFESP]Leon, Carlos Márcio Moura Ponce de [UNIFESP]Nogueira Filho, Pedro Antonio [UNIFESP]Wasinski, Frederick [UNIFESP]Araújo, Ronaldo de Carvalho [UNIFESP]Miranda, Antonio [UNIFESP]Ferreira, Alice Teixeira [UNIFESP]Paredes-Gamero, Edgar Julian [UNIFESP]2016-01-24T14:16:47Z2016-01-24T14:16:47Z2011-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion10https://dx.doi.org/10.1038/cddis.2011.49Cell Death & Disease. London: Nature Publishing Group, v. 2, 10 p., 2011.10.1038/cddis.2011.492041-4889https://repositorio.unifesp.br/handle/11600/33721WOS:000292243000001ark:/48912/00130000174dmengCell Death & Diseaseinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-10-07T15:55:21Zoai:repositorio.unifesp.br/:11600/33721Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T21:01:05.387103Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Differentiation of hematopoietic stem cell and myeloid populations by ATP is modulated by cytokines |
title |
Differentiation of hematopoietic stem cell and myeloid populations by ATP is modulated by cytokines |
spellingShingle |
Differentiation of hematopoietic stem cell and myeloid populations by ATP is modulated by cytokines Barbosa, Christiano Marcello Vaz [UNIFESP] ATP P2 receptors Hematopoietic stem cell Differentiation Myeloid Cytokines |
title_short |
Differentiation of hematopoietic stem cell and myeloid populations by ATP is modulated by cytokines |
title_full |
Differentiation of hematopoietic stem cell and myeloid populations by ATP is modulated by cytokines |
title_fullStr |
Differentiation of hematopoietic stem cell and myeloid populations by ATP is modulated by cytokines |
title_full_unstemmed |
Differentiation of hematopoietic stem cell and myeloid populations by ATP is modulated by cytokines |
title_sort |
Differentiation of hematopoietic stem cell and myeloid populations by ATP is modulated by cytokines |
author |
Barbosa, Christiano Marcello Vaz [UNIFESP] |
author_facet |
Barbosa, Christiano Marcello Vaz [UNIFESP] Leon, Carlos Márcio Moura Ponce de [UNIFESP] Nogueira Filho, Pedro Antonio [UNIFESP] Wasinski, Frederick [UNIFESP] Araújo, Ronaldo de Carvalho [UNIFESP] Miranda, Antonio [UNIFESP] Ferreira, Alice Teixeira [UNIFESP] Paredes-Gamero, Edgar Julian [UNIFESP] |
author_role |
author |
author2 |
Leon, Carlos Márcio Moura Ponce de [UNIFESP] Nogueira Filho, Pedro Antonio [UNIFESP] Wasinski, Frederick [UNIFESP] Araújo, Ronaldo de Carvalho [UNIFESP] Miranda, Antonio [UNIFESP] Ferreira, Alice Teixeira [UNIFESP] Paredes-Gamero, Edgar Julian [UNIFESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Barbosa, Christiano Marcello Vaz [UNIFESP] Leon, Carlos Márcio Moura Ponce de [UNIFESP] Nogueira Filho, Pedro Antonio [UNIFESP] Wasinski, Frederick [UNIFESP] Araújo, Ronaldo de Carvalho [UNIFESP] Miranda, Antonio [UNIFESP] Ferreira, Alice Teixeira [UNIFESP] Paredes-Gamero, Edgar Julian [UNIFESP] |
dc.subject.por.fl_str_mv |
ATP P2 receptors Hematopoietic stem cell Differentiation Myeloid Cytokines |
topic |
ATP P2 receptors Hematopoietic stem cell Differentiation Myeloid Cytokines |
description |
Extracellular nucleotides are emerging as important regulators of inflammation, cell proliferation and differentiation in a variety of tissues, including the hematopoietic system. in this study, the role of ATP was investigated during murine hematopoiesis. ATP was able to reduce the percentage of hematopoietic stem cells (HSCs), common myeloid progenitors and granulocyte-macrophage progenitors (GMPs), whereas differentiation into megakaryocyte-erythroid progenitors was not affected. in addition, in vivo administration of ATP to mice reduced the number of GMPs, but increased the number of Gr-1(+)Mac-1(+) myeloid cells. ATP also induced an increased proliferation rate and reduced Notch expression in HSCs and impaired HSC-mediated bone marrow reconstitution in sublethally irradiated mice. Moreover, the effects elicited by ATP were inhibited by suramin, a P2 receptor antagonist, and BAPTA, an intracellular Ca(2+) chelator. We further investigated whether the presence of cytokines might modulate the observed ATP-induced differentiation. Treatment of cells with cytokines (stem cell factor, interleukin-3 and granulocyte-monocyte colony stimulator factor) before ATP stimulation led to reduced ATP-dependent differentiation in long-term bone marrow cultures, thereby restoring the ability of HSCs to reconstitute hematopoiesis. Thus, our data suggest that ATP induces the differentiation of murine HSCs into the myeloid lineage and that this effect can be modulated by cytokines. Cell Death and Disease (2011) 2, e165; doi:10.1038/cddis.2011.49; published online 2 June 2011 |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-06-01 2016-01-24T14:16:47Z 2016-01-24T14:16:47Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://dx.doi.org/10.1038/cddis.2011.49 Cell Death & Disease. London: Nature Publishing Group, v. 2, 10 p., 2011. 10.1038/cddis.2011.49 2041-4889 https://repositorio.unifesp.br/handle/11600/33721 WOS:000292243000001 |
dc.identifier.dark.fl_str_mv |
ark:/48912/00130000174dm |
url |
https://dx.doi.org/10.1038/cddis.2011.49 https://repositorio.unifesp.br/handle/11600/33721 |
identifier_str_mv |
Cell Death & Disease. London: Nature Publishing Group, v. 2, 10 p., 2011. 10.1038/cddis.2011.49 2041-4889 WOS:000292243000001 ark:/48912/00130000174dm |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Cell Death & Disease |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
10 |
dc.publisher.none.fl_str_mv |
Nature Publishing Group |
publisher.none.fl_str_mv |
Nature Publishing Group |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1818602586369949696 |