Homing of canine multipotent mesenchymal stromal cells after epidural transplant in a rabbit model of compressive spinal cord injury

Detalhes bibliográficos
Autor(a) principal: Ramos, Mariana Cristina
Data de Publicação: 2020
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://hdl.handle.net/11449/204531
Resumo: Multipotent mesenchymal stromal cells (MSCs) have been presented by the scientific community is a promising alternative for the treatment of inflammatory, traumatic, vascular, and degenerative diseases of the central nervous system due to their anti-inflammatory, immunomodulatory, and neuroregenerative properties. One of the aspects that can affect the effectiveness of stem cell therapy is the transplantation route used. The aim of this study was to evaluate the homing of canine adipose derived MSCs (AdMSCs) transplanted via epidural injection in an experimental rabbit model of compressive spinal cord injury. New Zealand rabbits (n=8) were subjected to spinal cord injury induced by compression of the 10th thoracic segment. Immediately after the surgical procedure, the animals were subjected to the transplantation of marked AdMSCs with quantum dots through epidural injection between the L7–S1 spaces. Seven days after the transplant, the brain, spinal cord, lungs, kidney, spleen, and liver were collected and evaluated by bioluminescence imaging. The spinal cord segments L7–S1 and the thoracic injury site were evaluated by confocal microscopy to identify the presence of marked canine AdMSCs. Results showed that AdMSCs migrated to the thoracic spinal cord segment, lungs, brain, liver, and kidneys, and no bioluminescence was observed in the spleen. The presence of canine AdMSCs in the spinal cord indicates the capacity of these cells to overcome the dura mater and reach the transplantation site. Epidural delivery is feasible and minimally invasive and might be a good candidate for cell transplantation in the context of neurological diseases.
id UNSP_63ede5cfd365fb80a1e232ec5f7a73db
oai_identifier_str oai:repositorio.unesp.br:11449/204531
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Homing of canine multipotent mesenchymal stromal cells after epidural transplant in a rabbit model of compressive spinal cord injuryHoming de células estromais mesenquimais multipotentes caninas após transplante pela via epidural em modelo experimental de lesão raquimedular aguda em coelhosRastreabilidade celularCélulas estromais mesenquimaisTransplante xenogênicoVia epiduralTrauma medularStem cell trackingXenotransplantEpidural transplantationSpinal cord injuryMesenchymal stromal cellsMultipotent mesenchymal stromal cells (MSCs) have been presented by the scientific community is a promising alternative for the treatment of inflammatory, traumatic, vascular, and degenerative diseases of the central nervous system due to their anti-inflammatory, immunomodulatory, and neuroregenerative properties. One of the aspects that can affect the effectiveness of stem cell therapy is the transplantation route used. The aim of this study was to evaluate the homing of canine adipose derived MSCs (AdMSCs) transplanted via epidural injection in an experimental rabbit model of compressive spinal cord injury. New Zealand rabbits (n=8) were subjected to spinal cord injury induced by compression of the 10th thoracic segment. Immediately after the surgical procedure, the animals were subjected to the transplantation of marked AdMSCs with quantum dots through epidural injection between the L7–S1 spaces. Seven days after the transplant, the brain, spinal cord, lungs, kidney, spleen, and liver were collected and evaluated by bioluminescence imaging. The spinal cord segments L7–S1 and the thoracic injury site were evaluated by confocal microscopy to identify the presence of marked canine AdMSCs. Results showed that AdMSCs migrated to the thoracic spinal cord segment, lungs, brain, liver, and kidneys, and no bioluminescence was observed in the spleen. The presence of canine AdMSCs in the spinal cord indicates the capacity of these cells to overcome the dura mater and reach the transplantation site. Epidural delivery is feasible and minimally invasive and might be a good candidate for cell transplantation in the context of neurological diseases.As células estromais mesenquimais multipotentes (CTM) têm sido apresentadas pela comunidade científica como uma alternativa promissora no tratamento de doenças inflamatórias, traumáticas, vasculares e degenerativas do sistema nervoso central devido a suas propriedades anti-inflamatórias, imunomoduladoras e neuroregenerativas. Um dos fatores que podem afetar a eficácia da terapia celular é a via de transplante utilizada. O objetivo deste estudo foi avaliar o homing de CTMs derivadas do tecido adiposo caninas (AdCTMs) transplantadas pela via epidural em modelo experimental de lesão raquimedular aguda em coelhos. A lesão raquimedular foi induzida experimentalmente em 8 coelhos por compressão do segmento medular T10, imediatamente após os animais foram submetidos ao transplante de AdCTMs caninas marcadas com nanocristais Qtracker 655 pela via epidural entre os espaços L7-S1. Sete dias após o transplante, o homing das AdCTMs caninas foi avaliado na medula espinhal, encéfalo, fígado, rins, baço e pulmão por meio de detecção de fluorescência em imageador in vivo. Os segmentos medulares L7-S1 e local de lesão foram analisados em microscopia confocal para a presença de AdCTMs marcadas. Constatou-se a presença de AdCTMs caninas em local de lesão na medula espinhal e segmento L7-S1, houve marcação em encéfalo, pulmão, fígado e rins, não houve marcação em baço. A presença de AdCTMs na medula espinhal comprova a capacidade destas células passarem pela dura mater e atingirem o local de lesão. O transplante epidural é viável e minimamente invasivo, sendo um bom candidato para o uso em terapia celular no contexto de doenças neurológicas.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)CAPES: 001Universidade Estadual Paulista (Unesp)Amorim, Rogério Martins [UNESP]Universidade Estadual Paulista (Unesp)Ramos, Mariana Cristina2021-04-28T13:34:30Z2021-04-28T13:34:30Z2020-11-17info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfapplication/pdfhttp://hdl.handle.net/11449/20453133004064022P3porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESP2024-09-09T17:38:34Zoai:repositorio.unesp.br:11449/204531Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-09T17:38:34Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Homing of canine multipotent mesenchymal stromal cells after epidural transplant in a rabbit model of compressive spinal cord injury
Homing de células estromais mesenquimais multipotentes caninas após transplante pela via epidural em modelo experimental de lesão raquimedular aguda em coelhos
title Homing of canine multipotent mesenchymal stromal cells after epidural transplant in a rabbit model of compressive spinal cord injury
spellingShingle Homing of canine multipotent mesenchymal stromal cells after epidural transplant in a rabbit model of compressive spinal cord injury
Ramos, Mariana Cristina
Rastreabilidade celular
Células estromais mesenquimais
Transplante xenogênico
Via epidural
Trauma medular
Stem cell tracking
Xenotransplant
Epidural transplantation
Spinal cord injury
Mesenchymal stromal cells
title_short Homing of canine multipotent mesenchymal stromal cells after epidural transplant in a rabbit model of compressive spinal cord injury
title_full Homing of canine multipotent mesenchymal stromal cells after epidural transplant in a rabbit model of compressive spinal cord injury
title_fullStr Homing of canine multipotent mesenchymal stromal cells after epidural transplant in a rabbit model of compressive spinal cord injury
title_full_unstemmed Homing of canine multipotent mesenchymal stromal cells after epidural transplant in a rabbit model of compressive spinal cord injury
title_sort Homing of canine multipotent mesenchymal stromal cells after epidural transplant in a rabbit model of compressive spinal cord injury
author Ramos, Mariana Cristina
author_facet Ramos, Mariana Cristina
author_role author
dc.contributor.none.fl_str_mv Amorim, Rogério Martins [UNESP]
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Ramos, Mariana Cristina
dc.subject.por.fl_str_mv Rastreabilidade celular
Células estromais mesenquimais
Transplante xenogênico
Via epidural
Trauma medular
Stem cell tracking
Xenotransplant
Epidural transplantation
Spinal cord injury
Mesenchymal stromal cells
topic Rastreabilidade celular
Células estromais mesenquimais
Transplante xenogênico
Via epidural
Trauma medular
Stem cell tracking
Xenotransplant
Epidural transplantation
Spinal cord injury
Mesenchymal stromal cells
description Multipotent mesenchymal stromal cells (MSCs) have been presented by the scientific community is a promising alternative for the treatment of inflammatory, traumatic, vascular, and degenerative diseases of the central nervous system due to their anti-inflammatory, immunomodulatory, and neuroregenerative properties. One of the aspects that can affect the effectiveness of stem cell therapy is the transplantation route used. The aim of this study was to evaluate the homing of canine adipose derived MSCs (AdMSCs) transplanted via epidural injection in an experimental rabbit model of compressive spinal cord injury. New Zealand rabbits (n=8) were subjected to spinal cord injury induced by compression of the 10th thoracic segment. Immediately after the surgical procedure, the animals were subjected to the transplantation of marked AdMSCs with quantum dots through epidural injection between the L7–S1 spaces. Seven days after the transplant, the brain, spinal cord, lungs, kidney, spleen, and liver were collected and evaluated by bioluminescence imaging. The spinal cord segments L7–S1 and the thoracic injury site were evaluated by confocal microscopy to identify the presence of marked canine AdMSCs. Results showed that AdMSCs migrated to the thoracic spinal cord segment, lungs, brain, liver, and kidneys, and no bioluminescence was observed in the spleen. The presence of canine AdMSCs in the spinal cord indicates the capacity of these cells to overcome the dura mater and reach the transplantation site. Epidural delivery is feasible and minimally invasive and might be a good candidate for cell transplantation in the context of neurological diseases.
publishDate 2020
dc.date.none.fl_str_mv 2020-11-17
2021-04-28T13:34:30Z
2021-04-28T13:34:30Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/11449/204531
33004064022P3
url http://hdl.handle.net/11449/204531
identifier_str_mv 33004064022P3
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Universidade Estadual Paulista (Unesp)
publisher.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.source.none.fl_str_mv 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 repositoriounesp@unesp.br
_version_ 1810021323555995648