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In vitro differentiation capacity of human breastmilk stem cells: A systematic review

BACKGROUND: Mesenchymal stem cells are pluripotent cells that have the ability to generate cells from a cell line or in other cell types from different tissues but from the same origin. Although those cells have more limited differentiation capacity than embryonic stem cells, they are easily obtaine...

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Autores principales: Pacheco, Camila Maria Ribeiro, Ferreira, Priscila Elias, Saçaki, Claudia Sayuri, Tannous, Luana Alves, Zotarelli-Filho, Idiberto José, Guarita-Souza, Luiz Cesar, de Carvalho, Katherine Athayde Teixeira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851011/
https://www.ncbi.nlm.nih.gov/pubmed/31768226
http://dx.doi.org/10.4252/wjsc.v11.i11.1005
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author Pacheco, Camila Maria Ribeiro
Ferreira, Priscila Elias
Saçaki, Claudia Sayuri
Tannous, Luana Alves
Zotarelli-Filho, Idiberto José
Guarita-Souza, Luiz Cesar
de Carvalho, Katherine Athayde Teixeira
author_facet Pacheco, Camila Maria Ribeiro
Ferreira, Priscila Elias
Saçaki, Claudia Sayuri
Tannous, Luana Alves
Zotarelli-Filho, Idiberto José
Guarita-Souza, Luiz Cesar
de Carvalho, Katherine Athayde Teixeira
author_sort Pacheco, Camila Maria Ribeiro
collection PubMed
description BACKGROUND: Mesenchymal stem cells are pluripotent cells that have the ability to generate cells from a cell line or in other cell types from different tissues but from the same origin. Although those cells have more limited differentiation capacity than embryonic stem cells, they are easily obtained from somatic tissue and can be grown in large quantities. This characteristic of undifferentiated stem cells differentiating into different cell lines arouses strategies in regenerative medicine for the treatment of different diseases such as neurodegenerative diseases. AIM: To evaluate the cell differentiation capacity of human breastmilk stem cells for the three germ layers by a systematic review. METHODS: The searched databases were PubMed, EMBASE, OVID, and COCHRANE LIBRARY, published between 2007 and 2018 in the English language. All were in vitro studies for analysis of the "cell differentiation potential" in the literature using the keywords “human breastmilk,” “stem cells,” and keywords combined with the Boolean operator “NOT” were used to exclude those articles that had the word “CANCER” and their respective synonyms, which were previously consulted according to medical subject heading terms. PRISMA 2009 guidelines were followed in this study. RESULTS: A total of 315 titles and abstracts of articles were examined. From these, 21 were in common with more than one database, leaving 294 articles for analysis. Of that total, five publications met the inclusion criteria. When analyzing the publications, it was demonstrated that human breastmilk stem cells have a high cellular plasticity, exhibiting the ability to generate cells of all three germ layers, endoderm, mesoderm, and ectoderm, demonstrating their stemness. Those cells expressed the genes, TRA-1-60/81, octamer-binding transcription factor 4, and NANOG, of which NANOG, a critical regulator for self-renewal and maintenance, was the most highly expressed. Those cells have the ability to differentiate in vitro into adipocytes, chondrocytes, osteocytes, oligodendrocytes, astrocytes, and neurons as well hepatocytes, β-pancreatic cells, and cardiomyocytes. CONCLUSION: Although the literature has been scarce, the pluripotentiality of these cells represents great potential for tissue engineering and cellular therapy. Further studies for safe clinical translation are needed.
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spelling pubmed-68510112019-11-26 In vitro differentiation capacity of human breastmilk stem cells: A systematic review Pacheco, Camila Maria Ribeiro Ferreira, Priscila Elias Saçaki, Claudia Sayuri Tannous, Luana Alves Zotarelli-Filho, Idiberto José Guarita-Souza, Luiz Cesar de Carvalho, Katherine Athayde Teixeira World J Stem Cells Systematic Review BACKGROUND: Mesenchymal stem cells are pluripotent cells that have the ability to generate cells from a cell line or in other cell types from different tissues but from the same origin. Although those cells have more limited differentiation capacity than embryonic stem cells, they are easily obtained from somatic tissue and can be grown in large quantities. This characteristic of undifferentiated stem cells differentiating into different cell lines arouses strategies in regenerative medicine for the treatment of different diseases such as neurodegenerative diseases. AIM: To evaluate the cell differentiation capacity of human breastmilk stem cells for the three germ layers by a systematic review. METHODS: The searched databases were PubMed, EMBASE, OVID, and COCHRANE LIBRARY, published between 2007 and 2018 in the English language. All were in vitro studies for analysis of the "cell differentiation potential" in the literature using the keywords “human breastmilk,” “stem cells,” and keywords combined with the Boolean operator “NOT” were used to exclude those articles that had the word “CANCER” and their respective synonyms, which were previously consulted according to medical subject heading terms. PRISMA 2009 guidelines were followed in this study. RESULTS: A total of 315 titles and abstracts of articles were examined. From these, 21 were in common with more than one database, leaving 294 articles for analysis. Of that total, five publications met the inclusion criteria. When analyzing the publications, it was demonstrated that human breastmilk stem cells have a high cellular plasticity, exhibiting the ability to generate cells of all three germ layers, endoderm, mesoderm, and ectoderm, demonstrating their stemness. Those cells expressed the genes, TRA-1-60/81, octamer-binding transcription factor 4, and NANOG, of which NANOG, a critical regulator for self-renewal and maintenance, was the most highly expressed. Those cells have the ability to differentiate in vitro into adipocytes, chondrocytes, osteocytes, oligodendrocytes, astrocytes, and neurons as well hepatocytes, β-pancreatic cells, and cardiomyocytes. CONCLUSION: Although the literature has been scarce, the pluripotentiality of these cells represents great potential for tissue engineering and cellular therapy. Further studies for safe clinical translation are needed. Baishideng Publishing Group Inc 2019-11-26 2019-11-26 /pmc/articles/PMC6851011/ /pubmed/31768226 http://dx.doi.org/10.4252/wjsc.v11.i11.1005 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Systematic Review
Pacheco, Camila Maria Ribeiro
Ferreira, Priscila Elias
Saçaki, Claudia Sayuri
Tannous, Luana Alves
Zotarelli-Filho, Idiberto José
Guarita-Souza, Luiz Cesar
de Carvalho, Katherine Athayde Teixeira
In vitro differentiation capacity of human breastmilk stem cells: A systematic review
title In vitro differentiation capacity of human breastmilk stem cells: A systematic review
title_full In vitro differentiation capacity of human breastmilk stem cells: A systematic review
title_fullStr In vitro differentiation capacity of human breastmilk stem cells: A systematic review
title_full_unstemmed In vitro differentiation capacity of human breastmilk stem cells: A systematic review
title_short In vitro differentiation capacity of human breastmilk stem cells: A systematic review
title_sort in vitro differentiation capacity of human breastmilk stem cells: a systematic review
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851011/
https://www.ncbi.nlm.nih.gov/pubmed/31768226
http://dx.doi.org/10.4252/wjsc.v11.i11.1005
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