INFLUÊNCIA DO ENXERTO DE MÚSCULO ESQUELÉTICO NO PAVILHÃO AURICULAR NA REGENERAÇÃO MUSCULAR DE CAMUNDONGOS MDX
Autor(a) principal: | |
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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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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 |
_version_ |
1811823639948951552 |