INFLUÊNCIA DO ENXERTO DE MÚSCULO ESQUELÉTICO NO PAVILHÃO AURICULAR NA REGENERAÇÃO MUSCULAR DE CAMUNDONGOS MDX

Detalhes bibliográficos
Autor(a) principal: Leal, Anna Lúcia Rocha China
Data de Publicação: 2006
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da Universidade Federal Fluminense (RIUFF)
Texto Completo: https://app.uff.br/riuff/handle/1/17241
Resumo: Duchenne Muscular Dystrophy (DMD) it is a fatal X-linked Xp21 locus inflammatory myopathy that affects 1 at 3500 male born neonates. Main clinical manifestation is muscular weakness, respiratory complications and evolution for death by the end of adolescence. Molecular alteration due to deletion and/or mutations in the dystrophin gene cause marked alteration in the cytoarchitecture of the muscular tissue. Dystrophin is a sarcolemmal protein that interacts with Factin in the sarcoplasm and laminin (LN) in the extracelular matrix. This promotes stabilization of the sarcolemma and protection against damage induced by the muscular contraction. Mdx mouse, a spontaneous mutant of the C57BL10/ScSn colony, is considered the appropriate animal model for studies of the physiopathology of DMD muscular lesion. Unlike the human homologous, mdx mice do not develop a fatal disease. Mdx mice show efficient regeneration and maintenance of muscular function throughout the life, though presenting characteristic phases with prevalence of myonecrosis, muscular regeneration and/or fibrosis. Experimental model of ectopic muscle grafting in the pina auricular allows detailed study of factors influencing cellular migration and inflammation in the implanted microenvironment and at distal sites. The aim of this study was to analyze the impact of grafting soleus muscle from C57 non dystrophic mice in the pina auricular of mdx mice in the microenvironment of the graft and the regeneration of skeletal muscles Triceps brachii (close site), Soleus and Gastrocnemius (distal site). Mdx mice at 6 weeks (w) received implant of 2w old Soleus muscle from C57 mice. Mdx mice, controls (C57/C57) and mdx mice submitted to surgical stress (sham) were sacrificed at 7, 10 and 15 days post grafting (dpe). The ears with implanted graft and also skeletal muscles (triceps, soleus and gastrocnemius) were processed for histology hematoxylin-eosin to assess morphological alterations. Tissues were also processed for imunohistochemistry to establish changes in the muscular microenvironment. It was used immunolabeling for Laminin (LN); NCAM positive cells for presence of satellite/activated myoblasts cells and hematopoietic stem cells (Sca-1+). Mdx 10dpe, showed increased expression of LN in the T.brachii (p <0,001), in the soleus (p <0,001) and gastrocnemius (p <0,01) skeletal muscles. Further increase of NCAM+ was also observed in skeletal muscles (T.brachii, Soleus) of mdx-Enx but not in the gastrocnemius muscles of mdx-Enx (15 dpe) and sham mdx mice. Likewise skeletal muscles of sham and mdx-Enx showed augment of Sca-1+ cells. Altogether the results indicate that implantation of ectopic syngeneic graft increased LN expression, proliferation and/or migration Sca-1+ cells into areas of muscular lesion further promoting muscle regeneration as assessed by increased numbers of NCAM positive cells in mdx muscles.
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spelling INFLUÊNCIA DO ENXERTO DE MÚSCULO ESQUELÉTICO NO PAVILHÃO AURICULAR NA REGENERAÇÃO MUSCULAR DE CAMUNDONGOS MDXInfluence of the muscle graft skeletons in the ear in a regeneration of muscle MDX miceRegeneraçao muscularMúsculo esqueléticoDistrofia muscularMatriz extracelularCAMUNDONGORATODISTROFIA DE DUCHENNERegenerating muscle, skeletal muscle, muscular dystrophy, extracellular matrixCNPQ::CIENCIAS BIOLOGICAS::IMUNOLOGIADuchenne Muscular Dystrophy (DMD) it is a fatal X-linked Xp21 locus inflammatory myopathy that affects 1 at 3500 male born neonates. Main clinical manifestation is muscular weakness, respiratory complications and evolution for death by the end of adolescence. Molecular alteration due to deletion and/or mutations in the dystrophin gene cause marked alteration in the cytoarchitecture of the muscular tissue. Dystrophin is a sarcolemmal protein that interacts with Factin in the sarcoplasm and laminin (LN) in the extracelular matrix. This promotes stabilization of the sarcolemma and protection against damage induced by the muscular contraction. Mdx mouse, a spontaneous mutant of the C57BL10/ScSn colony, is considered the appropriate animal model for studies of the physiopathology of DMD muscular lesion. Unlike the human homologous, mdx mice do not develop a fatal disease. Mdx mice show efficient regeneration and maintenance of muscular function throughout the life, though presenting characteristic phases with prevalence of myonecrosis, muscular regeneration and/or fibrosis. Experimental model of ectopic muscle grafting in the pina auricular allows detailed study of factors influencing cellular migration and inflammation in the implanted microenvironment and at distal sites. The aim of this study was to analyze the impact of grafting soleus muscle from C57 non dystrophic mice in the pina auricular of mdx mice in the microenvironment of the graft and the regeneration of skeletal muscles Triceps brachii (close site), Soleus and Gastrocnemius (distal site). Mdx mice at 6 weeks (w) received implant of 2w old Soleus muscle from C57 mice. Mdx mice, controls (C57/C57) and mdx mice submitted to surgical stress (sham) were sacrificed at 7, 10 and 15 days post grafting (dpe). The ears with implanted graft and also skeletal muscles (triceps, soleus and gastrocnemius) were processed for histology hematoxylin-eosin to assess morphological alterations. Tissues were also processed for imunohistochemistry to establish changes in the muscular microenvironment. It was used immunolabeling for Laminin (LN); NCAM positive cells for presence of satellite/activated myoblasts cells and hematopoietic stem cells (Sca-1+). Mdx 10dpe, showed increased expression of LN in the T.brachii (p <0,001), in the soleus (p <0,001) and gastrocnemius (p <0,01) skeletal muscles. Further increase of NCAM+ was also observed in skeletal muscles (T.brachii, Soleus) of mdx-Enx but not in the gastrocnemius muscles of mdx-Enx (15 dpe) and sham mdx mice. Likewise skeletal muscles of sham and mdx-Enx showed augment of Sca-1+ cells. Altogether the results indicate that implantation of ectopic syngeneic graft increased LN expression, proliferation and/or migration Sca-1+ cells into areas of muscular lesion further promoting muscle regeneration as assessed by increased numbers of NCAM positive cells in mdx muscles.Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorDistrofia Muscular do tipo Duchenne (DMD) é uma miopatia inflamatória fatal ligada ao cromossomo X locus Xp21, que acomete cerca de 1 a cada 3500 neonatos do sexo masculino. A principal manifestação clínica é a fraqueza muscular precoce, deformidades musculares, complicações respiratórias e evolução para óbito ao final da adolescência. A alteração molecular, devido à deleção e/ou mutações no gene da distrofina acarreta defeitos na citoarquitetura do tecido muscular. Distrofina é uma proteína do citoesqueleto localizada abaixo do sarcolema, mediando interação entre a F-actina no sarcoplasma e laminina (LN) na matriz extracelular promovendo estabilização do sarcolema e proteção de danos induzidos pela contração muscular. O camundongo mdx, um mutante espontâneo da colônia de C57BL10/ScSn, é considerado o modelo animal mais adequado para o estudo da fisiopatologia da lesão muscular do tipo DMD. Contudo ao contrário do homólogo humano a mutação no mdx não determina uma doença fatal, ocorrendo regeneração eficiente e manutenção da funcionalidade do tecido muscular. O mdx apresenta fases com prevalência de mionecrose, regeneração muscular e resolução com reparo e cicatrização. O modelo de enxerto ectópico de músculo no pavilhão auricular possibilita o estudo detalhado de fatores que influenciam a migração celular e a inflamação no tecido implantado. Neste trabalho foi utilizado enxerto ectópico singênico de músculo solear na região dorsal do pavilhão auricular visando caracterizar o possível impacto na regeneração dos músculos tríceps (próximo ao enxerto) e do solear e gastrocnêmio, localizados de forma distal. Foram utilizados camundongos C57 e mdx machos com 2 e 6 semanas (s) Com 6 s de idade o mdx recebeu no pavilhão auricular, o implante de músculo solear de C57 de 2 s idade .As orelhas com os enxertos e os músculos tríceps, solear e gastrocnêmio do mdx e controles foram coletados para análise 7, 10 e 15 dias pós-enxerto (dpe). Para eliminar os possíveis efeitos do estresse nos resultados foi incluído grupo mdx sham submetido somente a cirurgia sem receber o enxerto. As orelhas com enxerto singênico (C57/C57), (C57/Mdx) e os músculos esqueléticos (gastrocnêmio, tríceps e solear) dos mdx com enxerto (Enx) foram processados, corados pela hematoxilina-eosina para caracterização do infiltrado celular e por imunohistoquimica para estudo do microambiente do músculo: expressão de laminina (LN), presença de células satélites (NCAM+) e células tronco hematopoiéticas (Sca-1+). Mdx 10dpe, apresentaram aumentos significativos na expressão de LN no tríceps(p<0,001), solear(p<0,001) e gastrocnêmio(p<0,01) Também foi observado aumento marcante na presença de células NCAM+ nos músculos do mdx Enx pós-enxerto em todas as idades, exceto no gastrocnêmio, exceto em15 dpe e também nos animais sham. Quanto à expressão de Sca-1, foram observados aumentos significativos nos músculos analisados de animais sham e mdx-Enx. Os resultados levam a concluir que o enxerto ectópico poderia estar influenciando a expressão de LN e de forma positiva ativação, proliferação e migração de células Sca-1positiva para áreas de lesão muscular, aumentando o número de células NCAM positivas no músculo do mdx com enxerto.Programa de Pós-graduação em NeuroimunologiaNeuroimunologiaSantos, Thereza Fonseca Quírico dosCPF:79186432622http://lattes.cnpq.br/0382591463869002Lannes-vieira, JoseliCPF:66655565422http://lattes.cnpq.br/6214934452403092Pons, Andrea HenriquesCPF:66786543122http://lattes.cnpq.br/0200106778993426Granjeiro, José MauroCPF:47892841722http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4784708U5Lagrota-candido, Jussara MachadoCPF:99888777622http://lattes.cnpq.br/4039085210526601Yamasaki, Edna NanamiCPF:78867757722http://lattes.cnpq.br/4724513941278427Leal, Anna Lúcia Rocha China2021-03-10T19:10:23Z2009-05-292021-03-10T19:10:23Z2006-06-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfapplication/pdfhttps://app.uff.br/riuff/handle/1/17241porCC-BY-SAinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da Universidade Federal Fluminense (RIUFF)instname:Universidade Federal Fluminense (UFF)instacron:UFF2021-03-10T19:10:23Zoai:app.uff.br:1/17241Repositório InstitucionalPUBhttps://app.uff.br/oai/requestriuff@id.uff.bropendoar:21202024-08-19T11:01:51.665346Repositório Institucional da Universidade Federal Fluminense (RIUFF) - Universidade Federal Fluminense (UFF)false
dc.title.none.fl_str_mv INFLUÊNCIA DO ENXERTO DE MÚSCULO ESQUELÉTICO NO PAVILHÃO AURICULAR NA REGENERAÇÃO MUSCULAR DE CAMUNDONGOS MDX
Influence of the muscle graft skeletons in the ear in a regeneration of muscle MDX mice
title INFLUÊNCIA DO ENXERTO DE MÚSCULO ESQUELÉTICO NO PAVILHÃO AURICULAR NA REGENERAÇÃO MUSCULAR DE CAMUNDONGOS MDX
spellingShingle INFLUÊNCIA DO ENXERTO DE MÚSCULO ESQUELÉTICO NO PAVILHÃO AURICULAR NA REGENERAÇÃO MUSCULAR DE CAMUNDONGOS MDX
Leal, Anna Lúcia Rocha China
Regeneraçao muscular
Músculo esquelético
Distrofia muscular
Matriz extracelular
CAMUNDONGO
RATO
DISTROFIA DE DUCHENNE
Regenerating muscle, skeletal muscle, muscular dystrophy, extracellular matrix
CNPQ::CIENCIAS BIOLOGICAS::IMUNOLOGIA
title_short INFLUÊNCIA DO ENXERTO DE MÚSCULO ESQUELÉTICO NO PAVILHÃO AURICULAR NA REGENERAÇÃO MUSCULAR DE CAMUNDONGOS MDX
title_full INFLUÊNCIA DO ENXERTO DE MÚSCULO ESQUELÉTICO NO PAVILHÃO AURICULAR NA REGENERAÇÃO MUSCULAR DE CAMUNDONGOS MDX
title_fullStr INFLUÊNCIA DO ENXERTO DE MÚSCULO ESQUELÉTICO NO PAVILHÃO AURICULAR NA REGENERAÇÃO MUSCULAR DE CAMUNDONGOS MDX
title_full_unstemmed INFLUÊNCIA DO ENXERTO DE MÚSCULO ESQUELÉTICO NO PAVILHÃO AURICULAR NA REGENERAÇÃO MUSCULAR DE CAMUNDONGOS MDX
title_sort INFLUÊNCIA DO ENXERTO DE MÚSCULO ESQUELÉTICO NO PAVILHÃO AURICULAR NA REGENERAÇÃO MUSCULAR DE CAMUNDONGOS MDX
author Leal, Anna Lúcia Rocha China
author_facet Leal, Anna Lúcia Rocha China
author_role author
dc.contributor.none.fl_str_mv Santos, Thereza Fonseca Quírico dos
CPF:79186432622
http://lattes.cnpq.br/0382591463869002
Lannes-vieira, Joseli
CPF:66655565422
http://lattes.cnpq.br/6214934452403092
Pons, Andrea Henriques
CPF:66786543122
http://lattes.cnpq.br/0200106778993426
Granjeiro, José Mauro
CPF:47892841722
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4784708U5
Lagrota-candido, Jussara Machado
CPF:99888777622
http://lattes.cnpq.br/4039085210526601
Yamasaki, Edna Nanami
CPF:78867757722
http://lattes.cnpq.br/4724513941278427
dc.contributor.author.fl_str_mv Leal, Anna Lúcia Rocha China
dc.subject.por.fl_str_mv Regeneraçao muscular
Músculo esquelético
Distrofia muscular
Matriz extracelular
CAMUNDONGO
RATO
DISTROFIA DE DUCHENNE
Regenerating muscle, skeletal muscle, muscular dystrophy, extracellular matrix
CNPQ::CIENCIAS BIOLOGICAS::IMUNOLOGIA
topic Regeneraçao muscular
Músculo esquelético
Distrofia muscular
Matriz extracelular
CAMUNDONGO
RATO
DISTROFIA DE DUCHENNE
Regenerating muscle, skeletal muscle, muscular dystrophy, extracellular matrix
CNPQ::CIENCIAS BIOLOGICAS::IMUNOLOGIA
description Duchenne Muscular Dystrophy (DMD) it is a fatal X-linked Xp21 locus inflammatory myopathy that affects 1 at 3500 male born neonates. Main clinical manifestation is muscular weakness, respiratory complications and evolution for death by the end of adolescence. Molecular alteration due to deletion and/or mutations in the dystrophin gene cause marked alteration in the cytoarchitecture of the muscular tissue. Dystrophin is a sarcolemmal protein that interacts with Factin in the sarcoplasm and laminin (LN) in the extracelular matrix. This promotes stabilization of the sarcolemma and protection against damage induced by the muscular contraction. Mdx mouse, a spontaneous mutant of the C57BL10/ScSn colony, is considered the appropriate animal model for studies of the physiopathology of DMD muscular lesion. Unlike the human homologous, mdx mice do not develop a fatal disease. Mdx mice show efficient regeneration and maintenance of muscular function throughout the life, though presenting characteristic phases with prevalence of myonecrosis, muscular regeneration and/or fibrosis. Experimental model of ectopic muscle grafting in the pina auricular allows detailed study of factors influencing cellular migration and inflammation in the implanted microenvironment and at distal sites. The aim of this study was to analyze the impact of grafting soleus muscle from C57 non dystrophic mice in the pina auricular of mdx mice in the microenvironment of the graft and the regeneration of skeletal muscles Triceps brachii (close site), Soleus and Gastrocnemius (distal site). Mdx mice at 6 weeks (w) received implant of 2w old Soleus muscle from C57 mice. Mdx mice, controls (C57/C57) and mdx mice submitted to surgical stress (sham) were sacrificed at 7, 10 and 15 days post grafting (dpe). The ears with implanted graft and also skeletal muscles (triceps, soleus and gastrocnemius) were processed for histology hematoxylin-eosin to assess morphological alterations. Tissues were also processed for imunohistochemistry to establish changes in the muscular microenvironment. It was used immunolabeling for Laminin (LN); NCAM positive cells for presence of satellite/activated myoblasts cells and hematopoietic stem cells (Sca-1+). Mdx 10dpe, showed increased expression of LN in the T.brachii (p <0,001), in the soleus (p <0,001) and gastrocnemius (p <0,01) skeletal muscles. Further increase of NCAM+ was also observed in skeletal muscles (T.brachii, Soleus) of mdx-Enx but not in the gastrocnemius muscles of mdx-Enx (15 dpe) and sham mdx mice. Likewise skeletal muscles of sham and mdx-Enx showed augment of Sca-1+ cells. Altogether the results indicate that implantation of ectopic syngeneic graft increased LN expression, proliferation and/or migration Sca-1+ cells into areas of muscular lesion further promoting muscle regeneration as assessed by increased numbers of NCAM positive cells in mdx muscles.
publishDate 2006
dc.date.none.fl_str_mv 2006-06-28
2009-05-29
2021-03-10T19:10:23Z
2021-03-10T19:10:23Z
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 https://app.uff.br/riuff/handle/1/17241
url https://app.uff.br/riuff/handle/1/17241
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv CC-BY-SA
info:eu-repo/semantics/openAccess
rights_invalid_str_mv CC-BY-SA
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Programa de Pós-graduação em Neuroimunologia
Neuroimunologia
publisher.none.fl_str_mv Programa de Pós-graduação em Neuroimunologia
Neuroimunologia
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal Fluminense (RIUFF)
instname:Universidade Federal Fluminense (UFF)
instacron:UFF
instname_str Universidade Federal Fluminense (UFF)
instacron_str UFF
institution UFF
reponame_str Repositório Institucional da Universidade Federal Fluminense (RIUFF)
collection Repositório Institucional da Universidade Federal Fluminense (RIUFF)
repository.name.fl_str_mv Repositório Institucional da Universidade Federal Fluminense (RIUFF) - Universidade Federal Fluminense (UFF)
repository.mail.fl_str_mv riuff@id.uff.br
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