Efeitos imunomodulatório e neuroprotetor da aplicação de células tronco mesenquimais alogênicas criopreservadas em ratos com trauma experimental de medula espinhal
| Ano de defesa: | 2015 |
|---|---|
| Autor(a) principal: | |
| Orientador(a): | |
| Banca de defesa: | |
| Tipo de documento: | Tese |
| Tipo de acesso: | Acesso aberto |
| Idioma: | por |
| Instituição de defesa: |
Universidade Federal de Minas Gerais
|
| Programa de Pós-Graduação: |
Não Informado pela instituição
|
| Departamento: |
Não Informado pela instituição
|
| País: |
Não Informado pela instituição
|
| Palavras-chave em Português: | |
| Link de acesso: | https://hdl.handle.net/1843/BUBD-A7PMKF |
Resumo: | The aim of the present study was to evaluate immunomodulatory and neuroprotective effects of cryopreserved allogenic mesenchymal stem cells (MSCs) aplication on experimental spinal cord injury. Therefore, Rattus norvegicus, Lewis, EGFP, were used for MSCs isolation, and Wistar for the spinal cord injury study. Three experimental groups were evaluated: negative control (NC), positive control (CP) and MSC, on five evaluation time: 24, 48, 72 hours and eight and 21 days after surgery. Motor function was assessed by BBB locomotor rating scale. Histopathology and immunohistochemistry were performed for measurement of inflammatory infiltration (CD68), of neuronal integrity (NeuN) and astrocyte activation (GFAP). IL-10, TNF-, IL-1, TGF-, BDNF, GDNF and VEGF gene transcripts measurement were performed by real time RT-PCR. When compared to the CP group, the MSC group showed higher motor function scores at 72 hours, 8 and 21 days, lesser CD68 expression at eight days and GFAP at 21 days. Furthermore, there was lesser white matter degeneration and higher NeuN expression in MSC group at 21 days. IL-10 expression was higher in the MSC group at 24 hours, GDNF 48 hours and 8 days and VEGF at 21 days. However it was observed in the MSC group lower TNF- expression at 8 and 21 days, and TGF- 24 hours and at 21 days. There were no differences in IL-1 and BDNF expression. The MSC administration reduced the inflammatory infiltrate, increased t neuronal integrity, decreased white matter degeneration and astrocytes activation after spinal cord injury. Additionally, the MSC increased IL-10, GDNF and VEGF expression, and the reduced TNF and TGF-. |
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2019-08-13T12:08:29Z2025-09-08T23:03:10Z2019-08-13T12:08:29Z2015-02-25https://hdl.handle.net/1843/BUBD-A7PMKFThe aim of the present study was to evaluate immunomodulatory and neuroprotective effects of cryopreserved allogenic mesenchymal stem cells (MSCs) aplication on experimental spinal cord injury. Therefore, Rattus norvegicus, Lewis, EGFP, were used for MSCs isolation, and Wistar for the spinal cord injury study. Three experimental groups were evaluated: negative control (NC), positive control (CP) and MSC, on five evaluation time: 24, 48, 72 hours and eight and 21 days after surgery. Motor function was assessed by BBB locomotor rating scale. Histopathology and immunohistochemistry were performed for measurement of inflammatory infiltration (CD68), of neuronal integrity (NeuN) and astrocyte activation (GFAP). IL-10, TNF-, IL-1, TGF-, BDNF, GDNF and VEGF gene transcripts measurement were performed by real time RT-PCR. When compared to the CP group, the MSC group showed higher motor function scores at 72 hours, 8 and 21 days, lesser CD68 expression at eight days and GFAP at 21 days. Furthermore, there was lesser white matter degeneration and higher NeuN expression in MSC group at 21 days. IL-10 expression was higher in the MSC group at 24 hours, GDNF 48 hours and 8 days and VEGF at 21 days. However it was observed in the MSC group lower TNF- expression at 8 and 21 days, and TGF- 24 hours and at 21 days. There were no differences in IL-1 and BDNF expression. The MSC administration reduced the inflammatory infiltrate, increased t neuronal integrity, decreased white matter degeneration and astrocytes activation after spinal cord injury. Additionally, the MSC increased IL-10, GDNF and VEGF expression, and the reduced TNF and TGF-.Universidade Federal de Minas GeraismesenquimaisCélulas troncoCriopreservaçãoTrauma de medula espinhalRato como animal de laboratórioCélulas tronco mesenquimaisCriopreservaçãoTraumatismos da medula espinhalEfeitos imunomodulatório e neuroprotetor da aplicação de células tronco mesenquimais alogênicas criopreservadas em ratos com trauma experimental de medula espinhalinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisIsabel Rodrigues Rosadoinfo:eu-repo/semantics/openAccessporreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMGEliane Goncalves de MeloAlfredo Miranda de GoesRogeria SerakidesObjetivou-se avaliar os efeitos imunomodulatório e neuroprotetor da aplicação de células tronco mesenquimais (CTM) alógenas e criopreservadas no trauma experimental de medula espinhal. Foram utilizados Rattus norvegicus, Lewis, eGFP para isolamento das CTM, e Wistar para estudo do trauma de medula espinhal. Avaliou-se três grupos experimentais: controle negativo (CN), controle positivo (CP) e CTM, em cinco tempos de avaliação: 24, 48, 72 horas e oito e 21 dias após a cirurgia. Avaliou-se a função motora dos animais pelo teste BBB. Realizou-se histopatologia e imunoistoquímica para quantificar infiltrado inflamatório (CD68), integridade neuronal (NeuN) e ativação de astrócitos (GFAP). Quantificou-se os transcritos gênicos para IL-10, TNF-, IL-1, TGF-, BDNF, GDNF e VEGF por RT-PCR em tempo real. Quando comparado ao grupo CP, o grupo CTM apresentou maiores escores nas avaliações de função motora 72 horas, 8 e 21 dias após trauma, e menor expressão de CD68 aos 8 dias e de GFAP aos 21 dias. Observou-se menor degeneração da substância branca e maior expressão de NeuN no grupo CTM aos 21 dias. A expressão de IL-10 foi maior no grupo CTM às 24 horas, de GDNF 48 horas e 8 dias e de VEGF aos 21 dias. No grupo CTM houve menor expressão de TNF- aos 8 e 21 dias e de TGF- 24 horas e aos 21 dias. Não houveram diferenças na expressão de IL-1 e BDNF. A administração de CTM reduziu o infiltrado inflamatório, aumentou a quantidade de neurônios íntegros, diminuiu a degeneração da substância branca e a ativação de astrócitos após trauma de medula espinhal. Adicionalmente, as CTM aumentaram expressão de IL-10, de GDNF e de VEGF, e reduziram as de TNF e TGF-.UFMGORIGINALtese_versao_final_pdf__1_.pdfapplication/pdf3474761https://repositorio.ufmg.br//bitstreams/18ed8792-0550-4d45-bb09-8f52101071e2/download321037e6118672953c24461abf8a4e77MD51trueAnonymousREADTEXTtese_versao_final_pdf__1_.pdf.txttext/plain164747https://repositorio.ufmg.br//bitstreams/16a26999-f1fa-48e7-a631-477baf4843da/download543e1733470534ec059ab0b819ee896fMD52falseAnonymousREAD1843/BUBD-A7PMKF2025-09-08 20:03:10.205open.accessoai:repositorio.ufmg.br:1843/BUBD-A7PMKFhttps://repositorio.ufmg.br/Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2025-09-08T23:03:10Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false |
| dc.title.none.fl_str_mv |
Efeitos imunomodulatório e neuroprotetor da aplicação de células tronco mesenquimais alogênicas criopreservadas em ratos com trauma experimental de medula espinhal |
| title |
Efeitos imunomodulatório e neuroprotetor da aplicação de células tronco mesenquimais alogênicas criopreservadas em ratos com trauma experimental de medula espinhal |
| spellingShingle |
Efeitos imunomodulatório e neuroprotetor da aplicação de células tronco mesenquimais alogênicas criopreservadas em ratos com trauma experimental de medula espinhal Isabel Rodrigues Rosado Rato como animal de laboratório Células tronco mesenquimais Criopreservação Traumatismos da medula espinhal mesenquimais Células tronco Criopreservação Trauma de medula espinhal |
| title_short |
Efeitos imunomodulatório e neuroprotetor da aplicação de células tronco mesenquimais alogênicas criopreservadas em ratos com trauma experimental de medula espinhal |
| title_full |
Efeitos imunomodulatório e neuroprotetor da aplicação de células tronco mesenquimais alogênicas criopreservadas em ratos com trauma experimental de medula espinhal |
| title_fullStr |
Efeitos imunomodulatório e neuroprotetor da aplicação de células tronco mesenquimais alogênicas criopreservadas em ratos com trauma experimental de medula espinhal |
| title_full_unstemmed |
Efeitos imunomodulatório e neuroprotetor da aplicação de células tronco mesenquimais alogênicas criopreservadas em ratos com trauma experimental de medula espinhal |
| title_sort |
Efeitos imunomodulatório e neuroprotetor da aplicação de células tronco mesenquimais alogênicas criopreservadas em ratos com trauma experimental de medula espinhal |
| author |
Isabel Rodrigues Rosado |
| author_facet |
Isabel Rodrigues Rosado |
| author_role |
author |
| dc.contributor.author.fl_str_mv |
Isabel Rodrigues Rosado |
| dc.subject.por.fl_str_mv |
Rato como animal de laboratório Células tronco mesenquimais Criopreservação Traumatismos da medula espinhal |
| topic |
Rato como animal de laboratório Células tronco mesenquimais Criopreservação Traumatismos da medula espinhal mesenquimais Células tronco Criopreservação Trauma de medula espinhal |
| dc.subject.other.none.fl_str_mv |
mesenquimais Células tronco Criopreservação Trauma de medula espinhal |
| description |
The aim of the present study was to evaluate immunomodulatory and neuroprotective effects of cryopreserved allogenic mesenchymal stem cells (MSCs) aplication on experimental spinal cord injury. Therefore, Rattus norvegicus, Lewis, EGFP, were used for MSCs isolation, and Wistar for the spinal cord injury study. Three experimental groups were evaluated: negative control (NC), positive control (CP) and MSC, on five evaluation time: 24, 48, 72 hours and eight and 21 days after surgery. Motor function was assessed by BBB locomotor rating scale. Histopathology and immunohistochemistry were performed for measurement of inflammatory infiltration (CD68), of neuronal integrity (NeuN) and astrocyte activation (GFAP). IL-10, TNF-, IL-1, TGF-, BDNF, GDNF and VEGF gene transcripts measurement were performed by real time RT-PCR. When compared to the CP group, the MSC group showed higher motor function scores at 72 hours, 8 and 21 days, lesser CD68 expression at eight days and GFAP at 21 days. Furthermore, there was lesser white matter degeneration and higher NeuN expression in MSC group at 21 days. IL-10 expression was higher in the MSC group at 24 hours, GDNF 48 hours and 8 days and VEGF at 21 days. However it was observed in the MSC group lower TNF- expression at 8 and 21 days, and TGF- 24 hours and at 21 days. There were no differences in IL-1 and BDNF expression. The MSC administration reduced the inflammatory infiltrate, increased t neuronal integrity, decreased white matter degeneration and astrocytes activation after spinal cord injury. Additionally, the MSC increased IL-10, GDNF and VEGF expression, and the reduced TNF and TGF-. |
| publishDate |
2015 |
| dc.date.issued.fl_str_mv |
2015-02-25 |
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2019-08-13T12:08:29Z 2025-09-08T23:03:10Z |
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2019-08-13T12:08:29Z |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/doctoralThesis |
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publishedVersion |
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https://hdl.handle.net/1843/BUBD-A7PMKF |
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https://hdl.handle.net/1843/BUBD-A7PMKF |
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por |
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por |
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info:eu-repo/semantics/openAccess |
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openAccess |
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Universidade Federal de Minas Gerais |
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Universidade Federal de Minas Gerais |
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