Isolation and characterization of mesenchymal stem cells derived from horse synovial liquid presenting the STRO-1 surface marker

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The biological properties of mesenchymal stem cells (MSCs) from synovial fluid from horse limb joints were analysed. The samples were characterized by their peculiarity of adhering to the plastic of the culture flasks. The electromagnetic field technique (MACS) and the surface biomarker STRO-1 were...

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Detalles Bibliográficos
Autores: Gonzales Figueroa, Hugo, Sen Wong, Yat, Gonzales Molfino, Hugo Mauricio, Llanos Carrillo, José Luis
Formato: artículo
Fecha de Publicación:2021
Institución:Universidad Nacional Mayor de San Marcos
Repositorio:Revistas - Universidad Nacional Mayor de San Marcos
Lenguaje:español
OAI Identifier:oai:ojs.csi.unmsm:article/21682
Enlace del recurso:https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/21682
Nivel de acceso:acceso abierto
Materia:mesenchymal stem cells
MSC
horse synovial fluid
biomarker
STRO-1
OCT4
NANOG
células madre mesenquimales
CMM
líquido sinovial de caballos
biomarcador
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oai_identifier_str oai:ojs.csi.unmsm:article/21682
network_acronym_str REVUNMSM
network_name_str Revistas - Universidad Nacional Mayor de San Marcos
repository_id_str
dc.title.none.fl_str_mv Isolation and characterization of mesenchymal stem cells derived from horse synovial liquid presenting the STRO-1 surface marker
Aislamiento y caracterización de las células madre mesenquimales derivadas de líquido sinovial de caballo que presentan el marcador de superficie STRO-1
title Isolation and characterization of mesenchymal stem cells derived from horse synovial liquid presenting the STRO-1 surface marker
spellingShingle Isolation and characterization of mesenchymal stem cells derived from horse synovial liquid presenting the STRO-1 surface marker
Gonzales Figueroa, Hugo
mesenchymal stem cells
MSC
horse synovial fluid
biomarker
STRO-1
OCT4
NANOG
células madre mesenquimales
CMM
líquido sinovial de caballos
biomarcador
STRO-1
OCT4
NANOG
title_short Isolation and characterization of mesenchymal stem cells derived from horse synovial liquid presenting the STRO-1 surface marker
title_full Isolation and characterization of mesenchymal stem cells derived from horse synovial liquid presenting the STRO-1 surface marker
title_fullStr Isolation and characterization of mesenchymal stem cells derived from horse synovial liquid presenting the STRO-1 surface marker
title_full_unstemmed Isolation and characterization of mesenchymal stem cells derived from horse synovial liquid presenting the STRO-1 surface marker
title_sort Isolation and characterization of mesenchymal stem cells derived from horse synovial liquid presenting the STRO-1 surface marker
dc.creator.none.fl_str_mv Gonzales Figueroa, Hugo
Sen Wong, Yat
Gonzales Molfino, Hugo Mauricio
Llanos Carrillo, José Luis
Gonzales Figueroa, Hugo
Sen Wong, Yat
Gonzales Molfino, Hugo Mauricio
Llanos Carrillo, José Luis
author Gonzales Figueroa, Hugo
author_facet Gonzales Figueroa, Hugo
Sen Wong, Yat
Gonzales Molfino, Hugo Mauricio
Llanos Carrillo, José Luis
author_role author
author2 Sen Wong, Yat
Gonzales Molfino, Hugo Mauricio
Llanos Carrillo, José Luis
author2_role author
author
author
dc.subject.none.fl_str_mv mesenchymal stem cells
MSC
horse synovial fluid
biomarker
STRO-1
OCT4
NANOG
células madre mesenquimales
CMM
líquido sinovial de caballos
biomarcador
STRO-1
OCT4
NANOG
topic mesenchymal stem cells
MSC
horse synovial fluid
biomarker
STRO-1
OCT4
NANOG
células madre mesenquimales
CMM
líquido sinovial de caballos
biomarcador
STRO-1
OCT4
NANOG
description The biological properties of mesenchymal stem cells (MSCs) from synovial fluid from horse limb joints were analysed. The samples were characterized by their peculiarity of adhering to the plastic of the culture flasks. The electromagnetic field technique (MACS) and the surface biomarker STRO-1 were used to optimize their isolation by enriching mesenchymal precursor cells (MSC-LS). To determine the expression of multipotency genes, total RNA was extracted and M-MLV reverse transcriptase was used for the cDNA, which served as a template for qPCR (quantitative PCR). qPCR was performed using the BioRad system with Sybr Green quantification. The multipotency genes quantified were OCT4 and NANOG. The cells selected using MACS with the surface biomarker STRO-1 (CMM-LS STRO-1) proliferate more rapidly than the CMM-LS obtained without purification. In addition, they showed a greater predisposition to differentiate into chondrocytes and osteocytes compared to non-purified LS-MSCs, and a lower predisposition to differentiate into adipocytes. Likewise, the expression of OCT-4 was significantly higher in the CMM-LS STRO-1 compared to the non-purified CMM-LS. NANOG expression was slightly higher in STRO-1 CMM-LS, but without significant differences. The results suggest that the co-expression of OCT-4 and Nanog could increase the physiological functions of MSC-LS STRO-1 related to better proliferation, self-renewal, and the predisposition to differentiate in osteochondral lineages; however, the functional role of these pluripotency markers in adult stem cells needs to be clarified.
publishDate 2021
dc.date.none.fl_str_mv 2021-12-22
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/21682
10.15381/rivep.v32i6.21682
url https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/21682
identifier_str_mv 10.15381/rivep.v32i6.21682
dc.language.none.fl_str_mv spa
language spa
dc.relation.none.fl_str_mv https://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/21682/17433
dc.rights.none.fl_str_mv http://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidad Nacional Mayor de San Marcos, Facultad de Medicina Veterinaria
publisher.none.fl_str_mv Universidad Nacional Mayor de San Marcos, Facultad de Medicina Veterinaria
dc.source.none.fl_str_mv Revista de Investigaciones Veterinarias del Perú; Vol. 32 Núm. 6 (2021); e21682
Revista de Investigaciones Veterinarias del Perú; Vol. 32 No. 6 (2021); e21682
1682-3419
1609-9117
reponame:Revistas - Universidad Nacional Mayor de San Marcos
instname:Universidad Nacional Mayor de San Marcos
instacron:UNMSM
instname_str Universidad Nacional Mayor de San Marcos
instacron_str UNMSM
institution UNMSM
reponame_str Revistas - Universidad Nacional Mayor de San Marcos
collection Revistas - Universidad Nacional Mayor de San Marcos
repository.name.fl_str_mv
repository.mail.fl_str_mv
_version_ 1795238236559245312
spelling Isolation and characterization of mesenchymal stem cells derived from horse synovial liquid presenting the STRO-1 surface markerAislamiento y caracterización de las células madre mesenquimales derivadas de líquido sinovial de caballo que presentan el marcador de superficie STRO-1Gonzales Figueroa, HugoSen Wong, YatGonzales Molfino, Hugo MauricioLlanos Carrillo, José LuisGonzales Figueroa, HugoSen Wong, YatGonzales Molfino, Hugo MauricioLlanos Carrillo, José Luismesenchymal stem cellsMSChorse synovial fluidbiomarkerSTRO-1OCT4NANOGcélulas madre mesenquimalesCMMlíquido sinovial de caballosbiomarcadorSTRO-1OCT4NANOGThe biological properties of mesenchymal stem cells (MSCs) from synovial fluid from horse limb joints were analysed. The samples were characterized by their peculiarity of adhering to the plastic of the culture flasks. The electromagnetic field technique (MACS) and the surface biomarker STRO-1 were used to optimize their isolation by enriching mesenchymal precursor cells (MSC-LS). To determine the expression of multipotency genes, total RNA was extracted and M-MLV reverse transcriptase was used for the cDNA, which served as a template for qPCR (quantitative PCR). qPCR was performed using the BioRad system with Sybr Green quantification. The multipotency genes quantified were OCT4 and NANOG. The cells selected using MACS with the surface biomarker STRO-1 (CMM-LS STRO-1) proliferate more rapidly than the CMM-LS obtained without purification. In addition, they showed a greater predisposition to differentiate into chondrocytes and osteocytes compared to non-purified LS-MSCs, and a lower predisposition to differentiate into adipocytes. Likewise, the expression of OCT-4 was significantly higher in the CMM-LS STRO-1 compared to the non-purified CMM-LS. NANOG expression was slightly higher in STRO-1 CMM-LS, but without significant differences. The results suggest that the co-expression of OCT-4 and Nanog could increase the physiological functions of MSC-LS STRO-1 related to better proliferation, self-renewal, and the predisposition to differentiate in osteochondral lineages; however, the functional role of these pluripotency markers in adult stem cells needs to be clarified.Se analizaron las propiedades biológicas de las células madre mesenquimales (CMM) provenientes del líquido sinovial de las articulaciones de las extremidades de caballo. Las muestras fueron caracterizadas por su peculiaridad de adherirse al plástico de los frascos de cultivos. Se utilizó la técnica de campos electromagnéticos (MACS) y el biomarcador de superficie STRO-1 con la finalidad de optimizar su aislamiento mediante el enriquecimiento de células precursoras mesenquimales (CMM-LS). Para determinar la expresión de los genes multipotencia, se extrajo el ARN total y se usó la transcriptasa reversa M-MLV para el ADNc, el que sirvió como molde para la qPCR (PCR cuantitativa). El qPCR se realizó utilizando el sistema BioRad con cuantificación mediante Sybr Green. Los genes de multipotencia cuantificados fueron OCT4 y NANOG. Las células seleccionadas utilizando MACS con el biomarcador de superficie STRO-1 (CMM-LS STRO-1), proliferan más rápidamente que las CMM-LS obtenidas sin purificar. Además, manifestaron una mayor predisposición a diferenciarse en condrocitos y osteocitos en comparación a las CMM-LS sin purificar, y una menor predisposición a diferenciarse en adipocitos. Así mismo, la expresión de OCT-4 fue significativamente superior en la CMM-LS STRO-1 en comparación con las CMM-LS sin purificar. La expresión de NANOG fue ligeramente superior en las CMM-LS STRO-1, pero sin diferencia significativa. Los resultados hacen suponer que la coexpresión de OCT-4 y Nanog podrían incrementar las funciones fisiológicas de las CMM-LS STRO-1 relacionadas con una mejor proliferación, autorrenovación y la predisposición a diferenciarse en los linajes osteocondrales; sin embargo, se necesita aclarar el papel funcional de estos marcadores de pluripotencia en células madre adultas.Universidad Nacional Mayor de San Marcos, Facultad de Medicina Veterinaria2021-12-22info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/2168210.15381/rivep.v32i6.21682Revista de Investigaciones Veterinarias del Perú; Vol. 32 Núm. 6 (2021); e21682Revista de Investigaciones Veterinarias del Perú; Vol. 32 No. 6 (2021); e216821682-34191609-9117reponame:Revistas - Universidad Nacional Mayor de San Marcosinstname:Universidad Nacional Mayor de San Marcosinstacron:UNMSMspahttps://revistasinvestigacion.unmsm.edu.pe/index.php/veterinaria/article/view/21682/17433Derechos de autor 2021 Hugo Gonzales Figueroa, Yat Sen Wong, Hugo Mauricio Gonzales Molfino, José Luis Llanos Carrillohttp://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessoai:ojs.csi.unmsm:article/216822021-12-27T16:45:12Z
score 13.924177
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