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Secretion pattern of canine amniotic stem cells derived extracellular vesicles

Extracellular vesicles (EVs) derived from stem cells (SCs) have regenerative potential and the possibility of being used in treating chronic diseases. EVs present lower risk of tumorigenicity and easily to isolation and storage. Therefore, this research aims to compare the morphological characterist...

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Autores principales: Karam, Rafael Garcia, Motta, Lina Castelo Branco, de Almeida, Matheus Ferreira, Bridi, Alessandra, da Silveira, Juliano Coelho, Ambrósio, Carlos Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Colégio Brasileiro de Reprodução Animal 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675050/
https://www.ncbi.nlm.nih.gov/pubmed/36425401
http://dx.doi.org/10.1590/1984-3143-AR2022-0063
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author Karam, Rafael Garcia
Motta, Lina Castelo Branco
de Almeida, Matheus Ferreira
Bridi, Alessandra
da Silveira, Juliano Coelho
Ambrósio, Carlos Eduardo
author_facet Karam, Rafael Garcia
Motta, Lina Castelo Branco
de Almeida, Matheus Ferreira
Bridi, Alessandra
da Silveira, Juliano Coelho
Ambrósio, Carlos Eduardo
author_sort Karam, Rafael Garcia
collection PubMed
description Extracellular vesicles (EVs) derived from stem cells (SCs) have regenerative potential and the possibility of being used in treating chronic diseases. EVs present lower risk of tumorigenicity and easily to isolation and storage. Therefore, this research aims to compare the morphological characteristics of the EVs (up to 150nm) derived from stem cells obtained from canine amniotic membranes in different passages during the in vitro culture. For this, cells from the amniotic membranes were isolated, cultured, and characterized. In order to answer our aim, the number of cells was normalized at each passage to generate conditioned media for EVs separation. The cells were differentiated into adipogenic, chondrogenic, and osteogenic tissue, to characterize these cells as mesenchymal stem cells (MSC). Moreover, flow cytometry analysis was performed and showed that the MSC were positive for CD90, CD105 and negative for CD34, CD45, mesenchymal and hematopoietic markers, respectively. For EVs analysis, MSC in different passages (P0-P2) were culture until 80% of confluence, then the medium was replaced by EVs depleted medium. After 48h, culture medium was collected and centrifuged to separate EVs, followed by nanoparticle tracking analysis. The EVs were also characterized by western blot and transmission electron microscopy (TEM). EVs were positive for Alix and negative for Cytochrome C as well as presented the traditional cup-shape by transmission electronic microscopy. Our results demonstrated that the concentration in the different passages was increased in P0 compared to P1 and P2 (p<0.05). No differences were found in EVs size (P0=132nm, P1=130nm and P2=120nm). Together, these results demonstrate that P0 of MSC is enriched of EVs when compared to later passages, suggesting that this passage would be the best to be applied in pre-clinical tests. Despite that, more studies are necessary to identify the EVs content and how the cells will respond to treatment with them.
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spelling pubmed-96750502022-11-23 Secretion pattern of canine amniotic stem cells derived extracellular vesicles Karam, Rafael Garcia Motta, Lina Castelo Branco de Almeida, Matheus Ferreira Bridi, Alessandra da Silveira, Juliano Coelho Ambrósio, Carlos Eduardo Anim Reprod Original Article Extracellular vesicles (EVs) derived from stem cells (SCs) have regenerative potential and the possibility of being used in treating chronic diseases. EVs present lower risk of tumorigenicity and easily to isolation and storage. Therefore, this research aims to compare the morphological characteristics of the EVs (up to 150nm) derived from stem cells obtained from canine amniotic membranes in different passages during the in vitro culture. For this, cells from the amniotic membranes were isolated, cultured, and characterized. In order to answer our aim, the number of cells was normalized at each passage to generate conditioned media for EVs separation. The cells were differentiated into adipogenic, chondrogenic, and osteogenic tissue, to characterize these cells as mesenchymal stem cells (MSC). Moreover, flow cytometry analysis was performed and showed that the MSC were positive for CD90, CD105 and negative for CD34, CD45, mesenchymal and hematopoietic markers, respectively. For EVs analysis, MSC in different passages (P0-P2) were culture until 80% of confluence, then the medium was replaced by EVs depleted medium. After 48h, culture medium was collected and centrifuged to separate EVs, followed by nanoparticle tracking analysis. The EVs were also characterized by western blot and transmission electron microscopy (TEM). EVs were positive for Alix and negative for Cytochrome C as well as presented the traditional cup-shape by transmission electronic microscopy. Our results demonstrated that the concentration in the different passages was increased in P0 compared to P1 and P2 (p<0.05). No differences were found in EVs size (P0=132nm, P1=130nm and P2=120nm). Together, these results demonstrate that P0 of MSC is enriched of EVs when compared to later passages, suggesting that this passage would be the best to be applied in pre-clinical tests. Despite that, more studies are necessary to identify the EVs content and how the cells will respond to treatment with them. Colégio Brasileiro de Reprodução Animal 2022-11-14 /pmc/articles/PMC9675050/ /pubmed/36425401 http://dx.doi.org/10.1590/1984-3143-AR2022-0063 Text en https://creativecommons.org/licenses/by/4.0/Copyright © The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Karam, Rafael Garcia
Motta, Lina Castelo Branco
de Almeida, Matheus Ferreira
Bridi, Alessandra
da Silveira, Juliano Coelho
Ambrósio, Carlos Eduardo
Secretion pattern of canine amniotic stem cells derived extracellular vesicles
title Secretion pattern of canine amniotic stem cells derived extracellular vesicles
title_full Secretion pattern of canine amniotic stem cells derived extracellular vesicles
title_fullStr Secretion pattern of canine amniotic stem cells derived extracellular vesicles
title_full_unstemmed Secretion pattern of canine amniotic stem cells derived extracellular vesicles
title_short Secretion pattern of canine amniotic stem cells derived extracellular vesicles
title_sort secretion pattern of canine amniotic stem cells derived extracellular vesicles
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675050/
https://www.ncbi.nlm.nih.gov/pubmed/36425401
http://dx.doi.org/10.1590/1984-3143-AR2022-0063
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