Regenerative potential of allogeneic adipose tissue-derived mesenchymal cells in canine cutaneous wounds

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BackgroundMesenchymal stem cells (MSCs) have generated a great amount of interest over the past decade as a novel therapeutic treatment for a variety of diseases. Emerging studies have indicated that MSCs could enhance the repair of injured skin in canine cutaneous wounds.Case presentationA healthy...

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Detalles Bibliográficos
Autores: Enciso, Nathaly, Avedillo, Luis, Fermin, Maria Luisa, Fragio, Cristina, Tejero, Concepcion
Formato: artículo
Fecha de Publicación:2020
Institución:Consejo Nacional de Ciencia Tecnología e Innovación
Repositorio:CONCYTEC-Institucional
Lenguaje:inglés
OAI Identifier:oai:repositorio.concytec.gob.pe:20.500.12390/2889
Enlace del recurso:https://hdl.handle.net/20.500.12390/2889
https://doi.org/10.1186/s13028-020-0511-z
Nivel de acceso:acceso abierto
Materia:General Veterinary
General Medicine
http://purl.org/pe-repo/ocde/ford#4.03.01
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oai_identifier_str oai:repositorio.concytec.gob.pe:20.500.12390/2889
network_acronym_str CONC
network_name_str CONCYTEC-Institucional
repository_id_str 4689
dc.title.none.fl_str_mv Regenerative potential of allogeneic adipose tissue-derived mesenchymal cells in canine cutaneous wounds
title Regenerative potential of allogeneic adipose tissue-derived mesenchymal cells in canine cutaneous wounds
spellingShingle Regenerative potential of allogeneic adipose tissue-derived mesenchymal cells in canine cutaneous wounds
Enciso, Nathaly
General Veterinary
General Medicine
http://purl.org/pe-repo/ocde/ford#4.03.01
title_short Regenerative potential of allogeneic adipose tissue-derived mesenchymal cells in canine cutaneous wounds
title_full Regenerative potential of allogeneic adipose tissue-derived mesenchymal cells in canine cutaneous wounds
title_fullStr Regenerative potential of allogeneic adipose tissue-derived mesenchymal cells in canine cutaneous wounds
title_full_unstemmed Regenerative potential of allogeneic adipose tissue-derived mesenchymal cells in canine cutaneous wounds
title_sort Regenerative potential of allogeneic adipose tissue-derived mesenchymal cells in canine cutaneous wounds
author Enciso, Nathaly
author_facet Enciso, Nathaly
Avedillo, Luis
Fermin, Maria Luisa
Fragio, Cristina
Tejero, Concepcion
author_role author
author2 Avedillo, Luis
Fermin, Maria Luisa
Fragio, Cristina
Tejero, Concepcion
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Enciso, Nathaly
Avedillo, Luis
Fermin, Maria Luisa
Fragio, Cristina
Tejero, Concepcion
dc.subject.none.fl_str_mv General Veterinary
topic General Veterinary
General Medicine
http://purl.org/pe-repo/ocde/ford#4.03.01
dc.subject.es_PE.fl_str_mv General Medicine
dc.subject.ocde.none.fl_str_mv http://purl.org/pe-repo/ocde/ford#4.03.01
description BackgroundMesenchymal stem cells (MSCs) have generated a great amount of interest over the past decade as a novel therapeutic treatment for a variety of diseases. Emerging studies have indicated that MSCs could enhance the repair of injured skin in canine cutaneous wounds.Case presentationA healthy 2 years old Bodeguero Andaluz dog was presented with multiple skin bite wounds. Antibiotic and anti-inflammatory therapy was administered for 8 days. On day three, 10(7) allogeneic adipose-derived mesenchymal stem cells (ASCs) were intradermally injected approximately equidistant to the ASCs treated wounds. Control wounds underwent conventional treatment with a topical antibacterial ointment until wound healing and closure. Wounds, skin morphology and healing progress were monitored via serial photographs and histopathology of biopsies obtained at day seven after ASC treatment. Histopathology revealed absence of inflammatory infiltrates and presence of multiple hair follicles in contrast to the non-ASCs treated control wounds indicating that ASC treatment promoted epidermal and dermal regeneration. ASCs were identified by flow cytometry and RT-PCR. The immunomodulatory role of ASCs was evidenced by coculturing peripheral blood mononuclear cells with allogeneic ASCs. Phytohemagglutinin was administered to stimulate lymphocyte proliferation. Cells were harvested and stained with an anticanine CD3-FITC antibody. The ASCs inhibited proliferation of T lymphocytes, which was quantified by reduction of carboxyfluorescein succinimidyl ester intensity using flow cytometry.ConclusionsCompared with conventional treatment, wounds treated with ASCs showed a higher regenerative capacity with earlier and faster closure in this dog.
publishDate 2020
dc.date.accessioned.none.fl_str_mv 2024-05-30T23:13:38Z
dc.date.available.none.fl_str_mv 2024-05-30T23:13:38Z
dc.date.issued.fl_str_mv 2020
dc.type.none.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.12390/2889
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1186/s13028-020-0511-z
url https://hdl.handle.net/20.500.12390/2889
https://doi.org/10.1186/s13028-020-0511-z
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv ACTA VETERINARIA SCANDINAVICA
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Springer Science and Business Media LLC
publisher.none.fl_str_mv Springer Science and Business Media LLC
dc.source.none.fl_str_mv reponame:CONCYTEC-Institucional
instname:Consejo Nacional de Ciencia Tecnología e Innovación
instacron:CONCYTEC
instname_str Consejo Nacional de Ciencia Tecnología e Innovación
instacron_str CONCYTEC
institution CONCYTEC
reponame_str CONCYTEC-Institucional
collection CONCYTEC-Institucional
repository.name.fl_str_mv Repositorio Institucional CONCYTEC
repository.mail.fl_str_mv repositorio@concytec.gob.pe
_version_ 1844883032581865472
spelling Publicationrp08047600rp08044600rp08046600rp08048600rp08045600Enciso, NathalyAvedillo, LuisFermin, Maria LuisaFragio, CristinaTejero, Concepcion2024-05-30T23:13:38Z2024-05-30T23:13:38Z2020https://hdl.handle.net/20.500.12390/2889https://doi.org/10.1186/s13028-020-0511-zBackgroundMesenchymal stem cells (MSCs) have generated a great amount of interest over the past decade as a novel therapeutic treatment for a variety of diseases. Emerging studies have indicated that MSCs could enhance the repair of injured skin in canine cutaneous wounds.Case presentationA healthy 2 years old Bodeguero Andaluz dog was presented with multiple skin bite wounds. Antibiotic and anti-inflammatory therapy was administered for 8 days. On day three, 10(7) allogeneic adipose-derived mesenchymal stem cells (ASCs) were intradermally injected approximately equidistant to the ASCs treated wounds. Control wounds underwent conventional treatment with a topical antibacterial ointment until wound healing and closure. Wounds, skin morphology and healing progress were monitored via serial photographs and histopathology of biopsies obtained at day seven after ASC treatment. Histopathology revealed absence of inflammatory infiltrates and presence of multiple hair follicles in contrast to the non-ASCs treated control wounds indicating that ASC treatment promoted epidermal and dermal regeneration. ASCs were identified by flow cytometry and RT-PCR. The immunomodulatory role of ASCs was evidenced by coculturing peripheral blood mononuclear cells with allogeneic ASCs. Phytohemagglutinin was administered to stimulate lymphocyte proliferation. Cells were harvested and stained with an anticanine CD3-FITC antibody. The ASCs inhibited proliferation of T lymphocytes, which was quantified by reduction of carboxyfluorescein succinimidyl ester intensity using flow cytometry.ConclusionsCompared with conventional treatment, wounds treated with ASCs showed a higher regenerative capacity with earlier and faster closure in this dog.Fondo Nacional de Desarrollo Científico y Tecnológico - FondecytengSpringer Science and Business Media LLCACTA VETERINARIA SCANDINAVICAinfo:eu-repo/semantics/openAccessGeneral VeterinaryGeneral Medicine-1http://purl.org/pe-repo/ocde/ford#4.03.01-1Regenerative potential of allogeneic adipose tissue-derived mesenchymal cells in canine cutaneous woundsinfo:eu-repo/semantics/articlereponame:CONCYTEC-Institucionalinstname:Consejo Nacional de Ciencia Tecnología e Innovacióninstacron:CONCYTEC#PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE#20.500.12390/2889oai:repositorio.concytec.gob.pe:20.500.12390/28892024-05-30 15:26:00.204http://purl.org/coar/access_right/c_14cbinfo:eu-repo/semantics/closedAccessmetadata only accesshttps://repositorio.concytec.gob.peRepositorio Institucional CONCYTECrepositorio@concytec.gob.pe#PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE#<Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="cf178a2e-71fe-45af-afde-3e105f18acc9"> <Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type> <Language>eng</Language> <Title>Regenerative potential of allogeneic adipose tissue-derived mesenchymal cells in canine cutaneous wounds</Title> <PublishedIn> <Publication> <Title>ACTA VETERINARIA SCANDINAVICA</Title> </Publication> </PublishedIn> <PublicationDate>2020</PublicationDate> <DOI>https://doi.org/10.1186/s13028-020-0511-z</DOI> <Authors> <Author> <DisplayName>Enciso, Nathaly</DisplayName> <Person id="rp08047" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Avedillo, Luis</DisplayName> <Person id="rp08044" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Fermin, Maria Luisa</DisplayName> <Person id="rp08046" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Fragio, Cristina</DisplayName> <Person id="rp08048" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Tejero, Concepcion</DisplayName> <Person id="rp08045" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> </Authors> <Editors> </Editors> <Publishers> <Publisher> <DisplayName>Springer Science and Business Media LLC</DisplayName> <OrgUnit /> </Publisher> </Publishers> <Keyword>General Veterinary</Keyword> <Keyword>General Medicine</Keyword> <Abstract>BackgroundMesenchymal stem cells (MSCs) have generated a great amount of interest over the past decade as a novel therapeutic treatment for a variety of diseases. Emerging studies have indicated that MSCs could enhance the repair of injured skin in canine cutaneous wounds.Case presentationA healthy 2 years old Bodeguero Andaluz dog was presented with multiple skin bite wounds. Antibiotic and anti-inflammatory therapy was administered for 8 days. On day three, 10(7) allogeneic adipose-derived mesenchymal stem cells (ASCs) were intradermally injected approximately equidistant to the ASCs treated wounds. Control wounds underwent conventional treatment with a topical antibacterial ointment until wound healing and closure. Wounds, skin morphology and healing progress were monitored via serial photographs and histopathology of biopsies obtained at day seven after ASC treatment. Histopathology revealed absence of inflammatory infiltrates and presence of multiple hair follicles in contrast to the non-ASCs treated control wounds indicating that ASC treatment promoted epidermal and dermal regeneration. ASCs were identified by flow cytometry and RT-PCR. The immunomodulatory role of ASCs was evidenced by coculturing peripheral blood mononuclear cells with allogeneic ASCs. Phytohemagglutinin was administered to stimulate lymphocyte proliferation. Cells were harvested and stained with an anticanine CD3-FITC antibody. The ASCs inhibited proliferation of T lymphocytes, which was quantified by reduction of carboxyfluorescein succinimidyl ester intensity using flow cytometry.ConclusionsCompared with conventional treatment, wounds treated with ASCs showed a higher regenerative capacity with earlier and faster closure in this dog.</Abstract> <Access xmlns="http://purl.org/coar/access_right" > </Access> </Publication> -1
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