Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulation
- Autores
- Avila Portillo, Luz M.; Aristizabal, Fabio; Riveros, Angela; Abba, Martín Carlos; Correa, Diego
- Año de publicación
- 2020
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Mesenchymal stem/stromal cells (MSCs) exhibit multidifferentiation potential, paralleled with immunomodulatory and trophic properties that make them viable alternative tools for the treatment of degenerative disorders, allograft rejection, autoimmune diseases, and tissue regeneration. MSC functional attributes can be modulated by exposing them to inflammatory-stimulating microenvironments (i.e., priming) before their therapeutic use. Granulocyte-colony stimulating factor (G-CSF) is a cytokine that plays key roles in immune response and hematopoiesis modulation through direct effects on hematopoietic progenitors' proliferation, survival, and mobilization. Despite the established roles of MSCs supporting hematopoiesis, the effects of G-CSF on MSCs biology have not been thoroughly explored. This study reveals that G-CSF has also direct effects on adipose-derived MSCs (ADSCs), modulating their functions. Herein, microarray-based transcriptomic analysis shows that G-CSF stimulation in vitro results in modulation of various signaling pathways including ones related with the metabolism of hyaluronan (HA), conferring a profile of cell mobilization to ADSCs, mediated in a cell-intrinsic fashion in part by reducing CD44 expression and HA synthesis-related genes. Collectively, these data suggest a direct modulatory effect of G-CSF on ADSC function, potentially altering their therapeutic capacity and thus the design of future clinical protocols.
Fil: Avila Portillo, Luz M.. Universidad Nacional de Colombia; Colombia
Fil: Aristizabal, Fabio. Universidad Nacional de Colombia; Colombia
Fil: Riveros, Angela. No especifíca;
Fil: Abba, Martín Carlos. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Centro de Investigaciones Inmunológicas Básicas y Aplicadas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata; Argentina
Fil: Correa, Diego. University of Miami; Estados Unidos - Materia
-
G-CSF
Mesenchymal
STEM
CELLS - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/131003
Ver los metadatos del registro completo
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Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulationAvila Portillo, Luz M.Aristizabal, FabioRiveros, AngelaAbba, Martín CarlosCorrea, DiegoG-CSFMesenchymalSTEMCELLShttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Mesenchymal stem/stromal cells (MSCs) exhibit multidifferentiation potential, paralleled with immunomodulatory and trophic properties that make them viable alternative tools for the treatment of degenerative disorders, allograft rejection, autoimmune diseases, and tissue regeneration. MSC functional attributes can be modulated by exposing them to inflammatory-stimulating microenvironments (i.e., priming) before their therapeutic use. Granulocyte-colony stimulating factor (G-CSF) is a cytokine that plays key roles in immune response and hematopoiesis modulation through direct effects on hematopoietic progenitors' proliferation, survival, and mobilization. Despite the established roles of MSCs supporting hematopoiesis, the effects of G-CSF on MSCs biology have not been thoroughly explored. This study reveals that G-CSF has also direct effects on adipose-derived MSCs (ADSCs), modulating their functions. Herein, microarray-based transcriptomic analysis shows that G-CSF stimulation in vitro results in modulation of various signaling pathways including ones related with the metabolism of hyaluronan (HA), conferring a profile of cell mobilization to ADSCs, mediated in a cell-intrinsic fashion in part by reducing CD44 expression and HA synthesis-related genes. Collectively, these data suggest a direct modulatory effect of G-CSF on ADSC function, potentially altering their therapeutic capacity and thus the design of future clinical protocols.Fil: Avila Portillo, Luz M.. Universidad Nacional de Colombia; ColombiaFil: Aristizabal, Fabio. Universidad Nacional de Colombia; ColombiaFil: Riveros, Angela. No especifíca;Fil: Abba, Martín Carlos. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Centro de Investigaciones Inmunológicas Básicas y Aplicadas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata; ArgentinaFil: Correa, Diego. University of Miami; Estados UnidosHindawi Publishing Corporation2020-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/131003Avila Portillo, Luz M.; Aristizabal, Fabio; Riveros, Angela; Abba, Martín Carlos; Correa, Diego; Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulation; Hindawi Publishing Corporation; Stem Cells International; 2020; 1-2020; 1-91687-9678CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1155/2020/5045124info:eu-repo/semantics/altIdentifier/url/https://www.hindawi.com/journals/sci/2020/5045124/info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:53:20Zoai:ri.conicet.gov.ar:11336/131003instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:53:21.216CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulation |
title |
Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulation |
spellingShingle |
Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulation Avila Portillo, Luz M. G-CSF Mesenchymal STEM CELLS |
title_short |
Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulation |
title_full |
Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulation |
title_fullStr |
Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulation |
title_full_unstemmed |
Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulation |
title_sort |
Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulation |
dc.creator.none.fl_str_mv |
Avila Portillo, Luz M. Aristizabal, Fabio Riveros, Angela Abba, Martín Carlos Correa, Diego |
author |
Avila Portillo, Luz M. |
author_facet |
Avila Portillo, Luz M. Aristizabal, Fabio Riveros, Angela Abba, Martín Carlos Correa, Diego |
author_role |
author |
author2 |
Aristizabal, Fabio Riveros, Angela Abba, Martín Carlos Correa, Diego |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
G-CSF Mesenchymal STEM CELLS |
topic |
G-CSF Mesenchymal STEM CELLS |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Mesenchymal stem/stromal cells (MSCs) exhibit multidifferentiation potential, paralleled with immunomodulatory and trophic properties that make them viable alternative tools for the treatment of degenerative disorders, allograft rejection, autoimmune diseases, and tissue regeneration. MSC functional attributes can be modulated by exposing them to inflammatory-stimulating microenvironments (i.e., priming) before their therapeutic use. Granulocyte-colony stimulating factor (G-CSF) is a cytokine that plays key roles in immune response and hematopoiesis modulation through direct effects on hematopoietic progenitors' proliferation, survival, and mobilization. Despite the established roles of MSCs supporting hematopoiesis, the effects of G-CSF on MSCs biology have not been thoroughly explored. This study reveals that G-CSF has also direct effects on adipose-derived MSCs (ADSCs), modulating their functions. Herein, microarray-based transcriptomic analysis shows that G-CSF stimulation in vitro results in modulation of various signaling pathways including ones related with the metabolism of hyaluronan (HA), conferring a profile of cell mobilization to ADSCs, mediated in a cell-intrinsic fashion in part by reducing CD44 expression and HA synthesis-related genes. Collectively, these data suggest a direct modulatory effect of G-CSF on ADSC function, potentially altering their therapeutic capacity and thus the design of future clinical protocols. Fil: Avila Portillo, Luz M.. Universidad Nacional de Colombia; Colombia Fil: Aristizabal, Fabio. Universidad Nacional de Colombia; Colombia Fil: Riveros, Angela. No especifíca; Fil: Abba, Martín Carlos. Universidad Nacional de La Plata. Facultad de Ciencias Médicas. Centro de Investigaciones Inmunológicas Básicas y Aplicadas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata; Argentina Fil: Correa, Diego. University of Miami; Estados Unidos |
description |
Mesenchymal stem/stromal cells (MSCs) exhibit multidifferentiation potential, paralleled with immunomodulatory and trophic properties that make them viable alternative tools for the treatment of degenerative disorders, allograft rejection, autoimmune diseases, and tissue regeneration. MSC functional attributes can be modulated by exposing them to inflammatory-stimulating microenvironments (i.e., priming) before their therapeutic use. Granulocyte-colony stimulating factor (G-CSF) is a cytokine that plays key roles in immune response and hematopoiesis modulation through direct effects on hematopoietic progenitors' proliferation, survival, and mobilization. Despite the established roles of MSCs supporting hematopoiesis, the effects of G-CSF on MSCs biology have not been thoroughly explored. This study reveals that G-CSF has also direct effects on adipose-derived MSCs (ADSCs), modulating their functions. Herein, microarray-based transcriptomic analysis shows that G-CSF stimulation in vitro results in modulation of various signaling pathways including ones related with the metabolism of hyaluronan (HA), conferring a profile of cell mobilization to ADSCs, mediated in a cell-intrinsic fashion in part by reducing CD44 expression and HA synthesis-related genes. Collectively, these data suggest a direct modulatory effect of G-CSF on ADSC function, potentially altering their therapeutic capacity and thus the design of future clinical protocols. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-01 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/131003 Avila Portillo, Luz M.; Aristizabal, Fabio; Riveros, Angela; Abba, Martín Carlos; Correa, Diego; Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulation; Hindawi Publishing Corporation; Stem Cells International; 2020; 1-2020; 1-9 1687-9678 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/131003 |
identifier_str_mv |
Avila Portillo, Luz M.; Aristizabal, Fabio; Riveros, Angela; Abba, Martín Carlos; Correa, Diego; Modulation of adipose-derived mesenchymal stem/stromal cell transcriptome by G-CSF stimulation; Hindawi Publishing Corporation; Stem Cells International; 2020; 1-2020; 1-9 1687-9678 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1155/2020/5045124 info:eu-repo/semantics/altIdentifier/url/https://www.hindawi.com/journals/sci/2020/5045124/ |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Hindawi Publishing Corporation |
publisher.none.fl_str_mv |
Hindawi Publishing Corporation |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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score |
13.13397 |