Human dental pulp stem cell monolayer and spheroid therapy after spinal motor root avulsion in adult rats

Detalhes bibliográficos
Autor(a) principal: Paes, Sabrina Moreira
Data de Publicação: 2023
Outros Autores: Castro, Mateus Vidigal de, Barbosa, Rafael Maza, Politti Cartarozzi, Luciana, Coser, Lilian de Oliveira, Kempe, Paula Regina Gelinski, Decarli, Monize Caiado, Moraes, Ângela Maria, Barraviera, Benedito [UNESP], Ferreira Júnior, Rui Seabra [UNESP], Oliveira, Alexandre Leite Rodrigues de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.brainres.2022.148229
http://hdl.handle.net/11449/248162
Resumo: Spinal cord injuries result in severe neurological deficits and neuronal loss, with poor functional recovery. Mesenchymal stem cells have shown promising results; therefore the present objective of this work was to compare motor recovery after treatment with human dental pulp stem cells (hDPSC) cultivated in monolayer (2D) or as spheroids (3D), following avulsion and reimplantation of spinal motor roots in adult rats. Thus, 72 adult female Lewis rats were divided into 4 groups: avulsion (AV); avulsion followed by reimplantation (AR); avulsion associated with reimplant and 2D cell therapy (AR + 2D), and avulsion associated with reimplant and 3D cell therapy (AR + 3D). The application of the cells in 2D and 3D was performed by microsurgery, with subsequent functional assessment using a walking track test (Catwalk system), immunohistochemistry, neuronal survival, and qRT-PCR in 1-, 4-, and 12-weeks post-injury. The animals in the AR + 2D and AR + 3D groups showed the highest neuronal survival rates, and immunofluorescence revealed downregulation of GFAP, and Iba-1, with preservation of synaptophysin, indicating a reduction in glial reactivity, combined with the maintenance of pre-synaptic inputs. There was an increase in anti-inflammatory (IL-4, TGFβ) and a reduction of pro-inflammatory factors (IL-6, TNFα) in animals treated with reimplantation and hDPSC. As for the functional recovery, in all analyzed parameters, the AR + 2D group performed better and was superior to the avulsion alone. Overall, our results indicate that the 2D and 3D cell therapy approaches provide successful immunomodulation and motor recovery, consistent with advanced therapies after spinal cord injury.
id UNSP_c55ecfb3b2e4204a7e07ff2b6664cfbd
oai_identifier_str oai:repositorio.unesp.br:11449/248162
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Human dental pulp stem cell monolayer and spheroid therapy after spinal motor root avulsion in adult ratsCell therapyDental pulpSpheroidSpinal cord injurySpinal cord injuries result in severe neurological deficits and neuronal loss, with poor functional recovery. Mesenchymal stem cells have shown promising results; therefore the present objective of this work was to compare motor recovery after treatment with human dental pulp stem cells (hDPSC) cultivated in monolayer (2D) or as spheroids (3D), following avulsion and reimplantation of spinal motor roots in adult rats. Thus, 72 adult female Lewis rats were divided into 4 groups: avulsion (AV); avulsion followed by reimplantation (AR); avulsion associated with reimplant and 2D cell therapy (AR + 2D), and avulsion associated with reimplant and 3D cell therapy (AR + 3D). The application of the cells in 2D and 3D was performed by microsurgery, with subsequent functional assessment using a walking track test (Catwalk system), immunohistochemistry, neuronal survival, and qRT-PCR in 1-, 4-, and 12-weeks post-injury. The animals in the AR + 2D and AR + 3D groups showed the highest neuronal survival rates, and immunofluorescence revealed downregulation of GFAP, and Iba-1, with preservation of synaptophysin, indicating a reduction in glial reactivity, combined with the maintenance of pre-synaptic inputs. There was an increase in anti-inflammatory (IL-4, TGFβ) and a reduction of pro-inflammatory factors (IL-6, TNFα) in animals treated with reimplantation and hDPSC. As for the functional recovery, in all analyzed parameters, the AR + 2D group performed better and was superior to the avulsion alone. Overall, our results indicate that the 2D and 3D cell therapy approaches provide successful immunomodulation and motor recovery, consistent with advanced therapies after spinal cord injury.Universidade Estadual PaulistaLaboratory of Nerve Regeneration Institute of Biology (IB) State University of Campinas (UNICAMP), SPSchool of Chemical Engineering University of Campinas UNICAMP, Av. Albert Einstein, 500Center for the Study of Venoms and Venomous Animals (CEVAP) São Paulo State University (UNESP), SPCenter for the Study of Venoms and Venomous Animals (CEVAP) São Paulo State University (UNESP), SPUniversidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (UNESP)Paes, Sabrina MoreiraCastro, Mateus Vidigal deBarbosa, Rafael MazaPolitti Cartarozzi, LucianaCoser, Lilian de OliveiraKempe, Paula Regina GelinskiDecarli, Monize CaiadoMoraes, Ângela MariaBarraviera, Benedito [UNESP]Ferreira Júnior, Rui Seabra [UNESP]Oliveira, Alexandre Leite Rodrigues de2023-07-29T13:36:11Z2023-07-29T13:36:11Z2023-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.brainres.2022.148229Brain Research, v. 1802.1872-62400006-8993http://hdl.handle.net/11449/24816210.1016/j.brainres.2022.1482292-s2.0-85145996529Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBrain Researchinfo:eu-repo/semantics/openAccess2024-04-11T15:28:26Zoai:repositorio.unesp.br:11449/248162Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-04-11T15:28:26Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Human dental pulp stem cell monolayer and spheroid therapy after spinal motor root avulsion in adult rats
title Human dental pulp stem cell monolayer and spheroid therapy after spinal motor root avulsion in adult rats
spellingShingle Human dental pulp stem cell monolayer and spheroid therapy after spinal motor root avulsion in adult rats
Paes, Sabrina Moreira
Cell therapy
Dental pulp
Spheroid
Spinal cord injury
title_short Human dental pulp stem cell monolayer and spheroid therapy after spinal motor root avulsion in adult rats
title_full Human dental pulp stem cell monolayer and spheroid therapy after spinal motor root avulsion in adult rats
title_fullStr Human dental pulp stem cell monolayer and spheroid therapy after spinal motor root avulsion in adult rats
title_full_unstemmed Human dental pulp stem cell monolayer and spheroid therapy after spinal motor root avulsion in adult rats
title_sort Human dental pulp stem cell monolayer and spheroid therapy after spinal motor root avulsion in adult rats
author Paes, Sabrina Moreira
author_facet Paes, Sabrina Moreira
Castro, Mateus Vidigal de
Barbosa, Rafael Maza
Politti Cartarozzi, Luciana
Coser, Lilian de Oliveira
Kempe, Paula Regina Gelinski
Decarli, Monize Caiado
Moraes, Ângela Maria
Barraviera, Benedito [UNESP]
Ferreira Júnior, Rui Seabra [UNESP]
Oliveira, Alexandre Leite Rodrigues de
author_role author
author2 Castro, Mateus Vidigal de
Barbosa, Rafael Maza
Politti Cartarozzi, Luciana
Coser, Lilian de Oliveira
Kempe, Paula Regina Gelinski
Decarli, Monize Caiado
Moraes, Ângela Maria
Barraviera, Benedito [UNESP]
Ferreira Júnior, Rui Seabra [UNESP]
Oliveira, Alexandre Leite Rodrigues de
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Paes, Sabrina Moreira
Castro, Mateus Vidigal de
Barbosa, Rafael Maza
Politti Cartarozzi, Luciana
Coser, Lilian de Oliveira
Kempe, Paula Regina Gelinski
Decarli, Monize Caiado
Moraes, Ângela Maria
Barraviera, Benedito [UNESP]
Ferreira Júnior, Rui Seabra [UNESP]
Oliveira, Alexandre Leite Rodrigues de
dc.subject.por.fl_str_mv Cell therapy
Dental pulp
Spheroid
Spinal cord injury
topic Cell therapy
Dental pulp
Spheroid
Spinal cord injury
description Spinal cord injuries result in severe neurological deficits and neuronal loss, with poor functional recovery. Mesenchymal stem cells have shown promising results; therefore the present objective of this work was to compare motor recovery after treatment with human dental pulp stem cells (hDPSC) cultivated in monolayer (2D) or as spheroids (3D), following avulsion and reimplantation of spinal motor roots in adult rats. Thus, 72 adult female Lewis rats were divided into 4 groups: avulsion (AV); avulsion followed by reimplantation (AR); avulsion associated with reimplant and 2D cell therapy (AR + 2D), and avulsion associated with reimplant and 3D cell therapy (AR + 3D). The application of the cells in 2D and 3D was performed by microsurgery, with subsequent functional assessment using a walking track test (Catwalk system), immunohistochemistry, neuronal survival, and qRT-PCR in 1-, 4-, and 12-weeks post-injury. The animals in the AR + 2D and AR + 3D groups showed the highest neuronal survival rates, and immunofluorescence revealed downregulation of GFAP, and Iba-1, with preservation of synaptophysin, indicating a reduction in glial reactivity, combined with the maintenance of pre-synaptic inputs. There was an increase in anti-inflammatory (IL-4, TGFβ) and a reduction of pro-inflammatory factors (IL-6, TNFα) in animals treated with reimplantation and hDPSC. As for the functional recovery, in all analyzed parameters, the AR + 2D group performed better and was superior to the avulsion alone. Overall, our results indicate that the 2D and 3D cell therapy approaches provide successful immunomodulation and motor recovery, consistent with advanced therapies after spinal cord injury.
publishDate 2023
dc.date.none.fl_str_mv 2023-07-29T13:36:11Z
2023-07-29T13:36:11Z
2023-03-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.brainres.2022.148229
Brain Research, v. 1802.
1872-6240
0006-8993
http://hdl.handle.net/11449/248162
10.1016/j.brainres.2022.148229
2-s2.0-85145996529
url http://dx.doi.org/10.1016/j.brainres.2022.148229
http://hdl.handle.net/11449/248162
identifier_str_mv Brain Research, v. 1802.
1872-6240
0006-8993
10.1016/j.brainres.2022.148229
2-s2.0-85145996529
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Brain Research
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1803047183553921024