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Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: Local or systemic?

BACKGROUND: The golden retriever muscular dystrophy (GRMD) dogs represent the best available animal model for therapeutic trials aiming at the future treatment of human Duchenne muscular dystrophy (DMD). We have obtained a rare litter of six GRMD dogs (3 males and 3 females) born from an affected ma...

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Autores principales: Kerkis, Irina, Ambrosio, Carlos E, Kerkis, Alexandre, Martins, Daniele S, Zucconi, Eder, Fonseca, Simone AS, Cabral, Rosa M, Maranduba, Carlos MC, Gaiad, Thais P, Morini, Adriana C, Vieira, Natassia M, Brolio, Marina P, Sant'Anna, Osvaldo A, Miglino, Maria A, Zatz, Mayana
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2529267/
https://www.ncbi.nlm.nih.gov/pubmed/18598348
http://dx.doi.org/10.1186/1479-5876-6-35
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author Kerkis, Irina
Ambrosio, Carlos E
Kerkis, Alexandre
Martins, Daniele S
Zucconi, Eder
Fonseca, Simone AS
Cabral, Rosa M
Maranduba, Carlos MC
Gaiad, Thais P
Morini, Adriana C
Vieira, Natassia M
Brolio, Marina P
Sant'Anna, Osvaldo A
Miglino, Maria A
Zatz, Mayana
author_facet Kerkis, Irina
Ambrosio, Carlos E
Kerkis, Alexandre
Martins, Daniele S
Zucconi, Eder
Fonseca, Simone AS
Cabral, Rosa M
Maranduba, Carlos MC
Gaiad, Thais P
Morini, Adriana C
Vieira, Natassia M
Brolio, Marina P
Sant'Anna, Osvaldo A
Miglino, Maria A
Zatz, Mayana
author_sort Kerkis, Irina
collection PubMed
description BACKGROUND: The golden retriever muscular dystrophy (GRMD) dogs represent the best available animal model for therapeutic trials aiming at the future treatment of human Duchenne muscular dystrophy (DMD). We have obtained a rare litter of six GRMD dogs (3 males and 3 females) born from an affected male and a carrier female which were submitted to a therapeutic trial with adult human stem cells to investigate their capacity to engraft into dogs muscles by local as compared to systemic injection without any immunosuppression. METHODS: Human Immature Dental Pulp Stem Cells (hIDPSC) were transplanted into 4 littermate dogs aged 28 to 40 days by either arterial or muscular injections. Two non-injected dogs were kept as controls. Clinical translation effects were analyzed since immune reactions by blood exams and physical scores capacity of each dog. Samples from biopsies were checked by immunohistochemistry (dystrophin markers) and FISH for human probes. RESULTS AND DISCUSSION: We analyzed the cells' ability in respect to migrate, engraftment, and myogenic potential, and the expression of human dystrophin in affected muscles. Additionally, the efficiency of single and consecutive early transplantation was compared. Chimeric muscle fibers were detected by immunofluorescence and fluorescent in situ hybridisation (FISH) using human antibodies and X and Y DNA probes. No signs of immune rejection were observed and these results suggested that hIDPSC cell transplantation may be done without immunosuppression. We showed that hIDPSC presented significant engraftment in GRMD dog muscles, although human dystrophin expression was modest and limited to several muscle fibers. Better clinical condition was also observed in the dog, which received monthly arterial injections and is still clinically stable at 25 months of age. CONCLUSION: Our data suggested that systemic multiple deliveries seemed more effective than local injections. These findings open important avenues for further researches.
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spelling pubmed-25292672008-09-05 Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: Local or systemic? Kerkis, Irina Ambrosio, Carlos E Kerkis, Alexandre Martins, Daniele S Zucconi, Eder Fonseca, Simone AS Cabral, Rosa M Maranduba, Carlos MC Gaiad, Thais P Morini, Adriana C Vieira, Natassia M Brolio, Marina P Sant'Anna, Osvaldo A Miglino, Maria A Zatz, Mayana J Transl Med Research BACKGROUND: The golden retriever muscular dystrophy (GRMD) dogs represent the best available animal model for therapeutic trials aiming at the future treatment of human Duchenne muscular dystrophy (DMD). We have obtained a rare litter of six GRMD dogs (3 males and 3 females) born from an affected male and a carrier female which were submitted to a therapeutic trial with adult human stem cells to investigate their capacity to engraft into dogs muscles by local as compared to systemic injection without any immunosuppression. METHODS: Human Immature Dental Pulp Stem Cells (hIDPSC) were transplanted into 4 littermate dogs aged 28 to 40 days by either arterial or muscular injections. Two non-injected dogs were kept as controls. Clinical translation effects were analyzed since immune reactions by blood exams and physical scores capacity of each dog. Samples from biopsies were checked by immunohistochemistry (dystrophin markers) and FISH for human probes. RESULTS AND DISCUSSION: We analyzed the cells' ability in respect to migrate, engraftment, and myogenic potential, and the expression of human dystrophin in affected muscles. Additionally, the efficiency of single and consecutive early transplantation was compared. Chimeric muscle fibers were detected by immunofluorescence and fluorescent in situ hybridisation (FISH) using human antibodies and X and Y DNA probes. No signs of immune rejection were observed and these results suggested that hIDPSC cell transplantation may be done without immunosuppression. We showed that hIDPSC presented significant engraftment in GRMD dog muscles, although human dystrophin expression was modest and limited to several muscle fibers. Better clinical condition was also observed in the dog, which received monthly arterial injections and is still clinically stable at 25 months of age. CONCLUSION: Our data suggested that systemic multiple deliveries seemed more effective than local injections. These findings open important avenues for further researches. BioMed Central 2008-07-03 /pmc/articles/PMC2529267/ /pubmed/18598348 http://dx.doi.org/10.1186/1479-5876-6-35 Text en Copyright © 2008 Kerkis et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Kerkis, Irina
Ambrosio, Carlos E
Kerkis, Alexandre
Martins, Daniele S
Zucconi, Eder
Fonseca, Simone AS
Cabral, Rosa M
Maranduba, Carlos MC
Gaiad, Thais P
Morini, Adriana C
Vieira, Natassia M
Brolio, Marina P
Sant'Anna, Osvaldo A
Miglino, Maria A
Zatz, Mayana
Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: Local or systemic?
title Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: Local or systemic?
title_full Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: Local or systemic?
title_fullStr Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: Local or systemic?
title_full_unstemmed Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: Local or systemic?
title_short Early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (GRMD) dogs: Local or systemic?
title_sort early transplantation of human immature dental pulp stem cells from baby teeth to golden retriever muscular dystrophy (grmd) dogs: local or systemic?
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2529267/
https://www.ncbi.nlm.nih.gov/pubmed/18598348
http://dx.doi.org/10.1186/1479-5876-6-35
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