The study of glial scar formation after brain ischemia using in-vitro strategies

Autores
Mannava, Raja Sekhar
Año de publicación
2015
Idioma
inglés
Tipo de recurso
tesis de maestría
Estado
versión aceptada
Colaborador/a o director/a de tesis
Mertelsmann, Roland
Murta, Verónica
Ramos, Alberto Javier
Rosenstein, Ruth
Garcia, Corina
Borner, Christoph
Descripción
Reactive gliosis is a generic response to Central Nervous System (CNS) injury mediated by astrocytes and microglia. Following ischemic damage to the CNS parenchyma, the injured area becomes surrounded by a dense astroglial cell layer known as glial scar. Glial scar formation has been recognized for many decades as a major impediment for neuronal reconnection and a serious obstacle for functional recovery. However, more recent studies have shown that scar limits the area of damage, preventing the diffusion of blood-derived activated immune cells into the CNS that could cause a generalized proinflammatory-neurodegenerative response.\nIn spite that it has been morphologically recognized for many years since Ramon y Cajal times, to study the biochemical signaling cascades involved in glial scar formation has been difficult mostly because of the in vivo nature of the process.\nIn this context, we studied here the mechanisms of glial scar assembly/disassembly in vitro to identify potential pharmacological targets for therapeutic interventions. To achieve this goal we will use the classical 2-Dimensional (2D) astroglial cultures, but we will also develop 3-dimensional (3D) astroglial cultures by using nanotube matrixes to attempt to better reproduce the in vivo situation. The results of this thesis showed that meningeal macrophages or ischemia-activated macrophages induce astroglial retraction and formation of scar-like structures in vitro. Scar-forming astrocytes over-express GFAP, S100B and TLR2-4. Using the NF-?B antagonist BAY-11-7082 we demonstrated that scar formation and its density is partially NF-?B dependent. Finally, in 3D astroglial culture grown on hydromatrix nanotubes, we showed that DAMPs can induce astroglial polarization but not the formation of the glial scar in vitro. We conclude that TLR/ NF-?B pathway is probably implicated in the glial scar formation or stabilization and that DAMPs and macrophages are necessary for the formation of glial scars in vitro.
Fil: Mannava, Raja Sekhar. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; Argentina
Magíster de la Universidad de Buenos Aires en Ciencias Biomédicas
Materia
Cicatriz glial
Isquemia cerebral
In-vitro
Brain ischemia
In vitro
Glial scar
Ciencia de la vida
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
Repositorio Digital Institucional de la Universidad de Buenos Aires
Institución
Universidad de Buenos Aires
OAI Identificador
oai:RDI UBA:afamaster:HWA_834

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spelling The study of glial scar formation after brain ischemia using in-vitro strategiesMannava, Raja SekharCicatriz glialIsquemia cerebralIn-vitroBrain ischemiaIn vitroGlial scarCiencia de la vidaReactive gliosis is a generic response to Central Nervous System (CNS) injury mediated by astrocytes and microglia. Following ischemic damage to the CNS parenchyma, the injured area becomes surrounded by a dense astroglial cell layer known as glial scar. Glial scar formation has been recognized for many decades as a major impediment for neuronal reconnection and a serious obstacle for functional recovery. However, more recent studies have shown that scar limits the area of damage, preventing the diffusion of blood-derived activated immune cells into the CNS that could cause a generalized proinflammatory-neurodegenerative response.\nIn spite that it has been morphologically recognized for many years since Ramon y Cajal times, to study the biochemical signaling cascades involved in glial scar formation has been difficult mostly because of the in vivo nature of the process.\nIn this context, we studied here the mechanisms of glial scar assembly/disassembly in vitro to identify potential pharmacological targets for therapeutic interventions. To achieve this goal we will use the classical 2-Dimensional (2D) astroglial cultures, but we will also develop 3-dimensional (3D) astroglial cultures by using nanotube matrixes to attempt to better reproduce the in vivo situation. The results of this thesis showed that meningeal macrophages or ischemia-activated macrophages induce astroglial retraction and formation of scar-like structures in vitro. Scar-forming astrocytes over-express GFAP, S100B and TLR2-4. Using the NF-?B antagonist BAY-11-7082 we demonstrated that scar formation and its density is partially NF-?B dependent. Finally, in 3D astroglial culture grown on hydromatrix nanotubes, we showed that DAMPs can induce astroglial polarization but not the formation of the glial scar in vitro. We conclude that TLR/ NF-?B pathway is probably implicated in the glial scar formation or stabilization and that DAMPs and macrophages are necessary for the formation of glial scars in vitro.Fil: Mannava, Raja Sekhar. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; ArgentinaMagíster de la Universidad de Buenos Aires en Ciencias BiomédicasUniversidad de Buenos Aires. Facultad de Farmacia y BioquímicaMertelsmann, RolandMurta, VerónicaRamos, Alberto JavierRosenstein, RuthGarcia, CorinaBorner, Christoph2015-06-01info:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/acceptedVersionhttp://purl.org/coar/resource_type/c_bdccinfo:ar-repo/semantics/tesisDeMaestriaapplication/pdfhttp://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=afamaster&cl=CL1&d=HWA_834https://repositoriouba.sisbi.uba.ar/gsdl/collect/afamaster/index/assoc/HWA_834.dir/834.PDFenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:Repositorio Digital Institucional de la Universidad de Buenos Airesinstname:Universidad de Buenos Aires2025-09-04T11:45:03Zoai:RDI UBA:afamaster:HWA_834instacron:UBAInstitucionalhttp://repositoriouba.sisbi.uba.ar/Universidad públicahttps://www.uba.ar/http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/oaiserver.cgicferrando@sisbi.uba.arArgentinaopendoar:2025-09-04 11:45:04.01Repositorio Digital Institucional de la Universidad de Buenos Aires - Universidad de Buenos Airesfalse
dc.title.none.fl_str_mv The study of glial scar formation after brain ischemia using in-vitro strategies
title The study of glial scar formation after brain ischemia using in-vitro strategies
spellingShingle The study of glial scar formation after brain ischemia using in-vitro strategies
Mannava, Raja Sekhar
Cicatriz glial
Isquemia cerebral
In-vitro
Brain ischemia
In vitro
Glial scar
Ciencia de la vida
title_short The study of glial scar formation after brain ischemia using in-vitro strategies
title_full The study of glial scar formation after brain ischemia using in-vitro strategies
title_fullStr The study of glial scar formation after brain ischemia using in-vitro strategies
title_full_unstemmed The study of glial scar formation after brain ischemia using in-vitro strategies
title_sort The study of glial scar formation after brain ischemia using in-vitro strategies
dc.creator.none.fl_str_mv Mannava, Raja Sekhar
author Mannava, Raja Sekhar
author_facet Mannava, Raja Sekhar
author_role author
dc.contributor.none.fl_str_mv Mertelsmann, Roland
Murta, Verónica
Ramos, Alberto Javier
Rosenstein, Ruth
Garcia, Corina
Borner, Christoph
dc.subject.none.fl_str_mv Cicatriz glial
Isquemia cerebral
In-vitro
Brain ischemia
In vitro
Glial scar
Ciencia de la vida
topic Cicatriz glial
Isquemia cerebral
In-vitro
Brain ischemia
In vitro
Glial scar
Ciencia de la vida
dc.description.none.fl_txt_mv Reactive gliosis is a generic response to Central Nervous System (CNS) injury mediated by astrocytes and microglia. Following ischemic damage to the CNS parenchyma, the injured area becomes surrounded by a dense astroglial cell layer known as glial scar. Glial scar formation has been recognized for many decades as a major impediment for neuronal reconnection and a serious obstacle for functional recovery. However, more recent studies have shown that scar limits the area of damage, preventing the diffusion of blood-derived activated immune cells into the CNS that could cause a generalized proinflammatory-neurodegenerative response.\nIn spite that it has been morphologically recognized for many years since Ramon y Cajal times, to study the biochemical signaling cascades involved in glial scar formation has been difficult mostly because of the in vivo nature of the process.\nIn this context, we studied here the mechanisms of glial scar assembly/disassembly in vitro to identify potential pharmacological targets for therapeutic interventions. To achieve this goal we will use the classical 2-Dimensional (2D) astroglial cultures, but we will also develop 3-dimensional (3D) astroglial cultures by using nanotube matrixes to attempt to better reproduce the in vivo situation. The results of this thesis showed that meningeal macrophages or ischemia-activated macrophages induce astroglial retraction and formation of scar-like structures in vitro. Scar-forming astrocytes over-express GFAP, S100B and TLR2-4. Using the NF-?B antagonist BAY-11-7082 we demonstrated that scar formation and its density is partially NF-?B dependent. Finally, in 3D astroglial culture grown on hydromatrix nanotubes, we showed that DAMPs can induce astroglial polarization but not the formation of the glial scar in vitro. We conclude that TLR/ NF-?B pathway is probably implicated in the glial scar formation or stabilization and that DAMPs and macrophages are necessary for the formation of glial scars in vitro.
Fil: Mannava, Raja Sekhar. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; Argentina
Magíster de la Universidad de Buenos Aires en Ciencias Biomédicas
description Reactive gliosis is a generic response to Central Nervous System (CNS) injury mediated by astrocytes and microglia. Following ischemic damage to the CNS parenchyma, the injured area becomes surrounded by a dense astroglial cell layer known as glial scar. Glial scar formation has been recognized for many decades as a major impediment for neuronal reconnection and a serious obstacle for functional recovery. However, more recent studies have shown that scar limits the area of damage, preventing the diffusion of blood-derived activated immune cells into the CNS that could cause a generalized proinflammatory-neurodegenerative response.\nIn spite that it has been morphologically recognized for many years since Ramon y Cajal times, to study the biochemical signaling cascades involved in glial scar formation has been difficult mostly because of the in vivo nature of the process.\nIn this context, we studied here the mechanisms of glial scar assembly/disassembly in vitro to identify potential pharmacological targets for therapeutic interventions. To achieve this goal we will use the classical 2-Dimensional (2D) astroglial cultures, but we will also develop 3-dimensional (3D) astroglial cultures by using nanotube matrixes to attempt to better reproduce the in vivo situation. The results of this thesis showed that meningeal macrophages or ischemia-activated macrophages induce astroglial retraction and formation of scar-like structures in vitro. Scar-forming astrocytes over-express GFAP, S100B and TLR2-4. Using the NF-?B antagonist BAY-11-7082 we demonstrated that scar formation and its density is partially NF-?B dependent. Finally, in 3D astroglial culture grown on hydromatrix nanotubes, we showed that DAMPs can induce astroglial polarization but not the formation of the glial scar in vitro. We conclude that TLR/ NF-?B pathway is probably implicated in the glial scar formation or stabilization and that DAMPs and macrophages are necessary for the formation of glial scars in vitro.
publishDate 2015
dc.date.none.fl_str_mv 2015-06-01
dc.type.none.fl_str_mv info:eu-repo/semantics/masterThesis
info:eu-repo/semantics/acceptedVersion
http://purl.org/coar/resource_type/c_bdcc
info:ar-repo/semantics/tesisDeMaestria
format masterThesis
status_str acceptedVersion
dc.identifier.none.fl_str_mv http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=afamaster&cl=CL1&d=HWA_834
https://repositoriouba.sisbi.uba.ar/gsdl/collect/afamaster/index/assoc/HWA_834.dir/834.PDF
url http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=afamaster&cl=CL1&d=HWA_834
https://repositoriouba.sisbi.uba.ar/gsdl/collect/afamaster/index/assoc/HWA_834.dir/834.PDF
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica
publisher.none.fl_str_mv Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica
dc.source.none.fl_str_mv reponame:Repositorio Digital Institucional de la Universidad de Buenos Aires
instname:Universidad de Buenos Aires
reponame_str Repositorio Digital Institucional de la Universidad de Buenos Aires
collection Repositorio Digital Institucional de la Universidad de Buenos Aires
instname_str Universidad de Buenos Aires
repository.name.fl_str_mv Repositorio Digital Institucional de la Universidad de Buenos Aires - Universidad de Buenos Aires
repository.mail.fl_str_mv cferrando@sisbi.uba.ar
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