Micromass cultures are effective for differentiation of human amniotic fluid stem cells into chondrocytes

Detalhes bibliográficos
Autor(a) principal: Zuliani, Carolina Coli
Data de Publicação: 2018
Outros Autores: Bombini, Mariana Freschi, Andrade, Kleber Cursino de, Mamoni, Ronei, Pereira, Ana Helena, Coimbra, Ibsen Bellini
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/146255
Resumo: OBJECTIVES: Articular cartilage is vulnerable to injuries and undergoes an irreversible degenerative process. The use of amniotic fluid mesenchymal stromal stem cells for the reconstruction of articular cartilage is a promising therapeutic alternative. The aim of this study was to investigate the chondrogenic potential of amniotic fluid mesenchymal stromal stem cells from human amniotic fluid from second trimester pregnant women in a micromass system (high-density cell culture) with TGF-β3 for 21 days. METHODS: Micromass was performed using amniotic fluid mesenchymal stromal stem cells previously cultured in a monolayer. Chondrocytes from adult human normal cartilage were used as controls. After 21 days, chondrogenic potential was determined by measuring the expression of genes, such as SOX-9, type II collagen and aggrecan, in newly differentiated cells by real-time PCR (qRT-PCR). The production of type II collagen protein was observed by western blotting. Immunohistochemistry analysis was also performed to detect collagen type II and aggrecan. This study was approved by the local ethics committee. RESULTS: SOX-9, aggrecan and type II collagen were expressed in newly differentiated chondrocytes. The expression of SOX-9 was significantly higher in newly differentiated chondrocytes than in adult cartilage. Collagen type II protein was also detected. CONCLUSION: We demonstrate that stem cells from human amniotic fluid are a suitable source for chondrogenesis when cultured in a micromass system. amniotic fluid mesenchymal stromal stem cells are an extremely viable source for clinical applications, and our results suggest the possibility of using human amniotic fluid as a source of mesenchymal stem cells.
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spelling Micromass cultures are effective for differentiation of human amniotic fluid stem cells into chondrocytesCartilage RepairChondrogenesisAmniotic Fluid Mesenchymal Stromal Stem CellsMicromass CultureOBJECTIVES: Articular cartilage is vulnerable to injuries and undergoes an irreversible degenerative process. The use of amniotic fluid mesenchymal stromal stem cells for the reconstruction of articular cartilage is a promising therapeutic alternative. The aim of this study was to investigate the chondrogenic potential of amniotic fluid mesenchymal stromal stem cells from human amniotic fluid from second trimester pregnant women in a micromass system (high-density cell culture) with TGF-β3 for 21 days. METHODS: Micromass was performed using amniotic fluid mesenchymal stromal stem cells previously cultured in a monolayer. Chondrocytes from adult human normal cartilage were used as controls. After 21 days, chondrogenic potential was determined by measuring the expression of genes, such as SOX-9, type II collagen and aggrecan, in newly differentiated cells by real-time PCR (qRT-PCR). The production of type II collagen protein was observed by western blotting. Immunohistochemistry analysis was also performed to detect collagen type II and aggrecan. This study was approved by the local ethics committee. RESULTS: SOX-9, aggrecan and type II collagen were expressed in newly differentiated chondrocytes. The expression of SOX-9 was significantly higher in newly differentiated chondrocytes than in adult cartilage. Collagen type II protein was also detected. CONCLUSION: We demonstrate that stem cells from human amniotic fluid are a suitable source for chondrogenesis when cultured in a micromass system. amniotic fluid mesenchymal stromal stem cells are an extremely viable source for clinical applications, and our results suggest the possibility of using human amniotic fluid as a source of mesenchymal stem cells.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2018-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/14625510.6061/clinics/2018/e268Clinics; Vol. 73 (2018); e268Clinics; v. 73 (2018); e268Clinics; Vol. 73 (2018); e2681980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/146255/139944Copyright (c) 2018 Clinicsinfo:eu-repo/semantics/openAccessZuliani, Carolina ColiBombini, Mariana FreschiAndrade, Kleber Cursino deMamoni, RoneiPereira, Ana HelenaCoimbra, Ibsen Bellini2019-05-14T11:48:50Zoai:revistas.usp.br:article/146255Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2019-05-14T11:48:50Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Micromass cultures are effective for differentiation of human amniotic fluid stem cells into chondrocytes
title Micromass cultures are effective for differentiation of human amniotic fluid stem cells into chondrocytes
spellingShingle Micromass cultures are effective for differentiation of human amniotic fluid stem cells into chondrocytes
Zuliani, Carolina Coli
Cartilage Repair
Chondrogenesis
Amniotic Fluid Mesenchymal Stromal Stem Cells
Micromass Culture
title_short Micromass cultures are effective for differentiation of human amniotic fluid stem cells into chondrocytes
title_full Micromass cultures are effective for differentiation of human amniotic fluid stem cells into chondrocytes
title_fullStr Micromass cultures are effective for differentiation of human amniotic fluid stem cells into chondrocytes
title_full_unstemmed Micromass cultures are effective for differentiation of human amniotic fluid stem cells into chondrocytes
title_sort Micromass cultures are effective for differentiation of human amniotic fluid stem cells into chondrocytes
author Zuliani, Carolina Coli
author_facet Zuliani, Carolina Coli
Bombini, Mariana Freschi
Andrade, Kleber Cursino de
Mamoni, Ronei
Pereira, Ana Helena
Coimbra, Ibsen Bellini
author_role author
author2 Bombini, Mariana Freschi
Andrade, Kleber Cursino de
Mamoni, Ronei
Pereira, Ana Helena
Coimbra, Ibsen Bellini
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Zuliani, Carolina Coli
Bombini, Mariana Freschi
Andrade, Kleber Cursino de
Mamoni, Ronei
Pereira, Ana Helena
Coimbra, Ibsen Bellini
dc.subject.por.fl_str_mv Cartilage Repair
Chondrogenesis
Amniotic Fluid Mesenchymal Stromal Stem Cells
Micromass Culture
topic Cartilage Repair
Chondrogenesis
Amniotic Fluid Mesenchymal Stromal Stem Cells
Micromass Culture
description OBJECTIVES: Articular cartilage is vulnerable to injuries and undergoes an irreversible degenerative process. The use of amniotic fluid mesenchymal stromal stem cells for the reconstruction of articular cartilage is a promising therapeutic alternative. The aim of this study was to investigate the chondrogenic potential of amniotic fluid mesenchymal stromal stem cells from human amniotic fluid from second trimester pregnant women in a micromass system (high-density cell culture) with TGF-β3 for 21 days. METHODS: Micromass was performed using amniotic fluid mesenchymal stromal stem cells previously cultured in a monolayer. Chondrocytes from adult human normal cartilage were used as controls. After 21 days, chondrogenic potential was determined by measuring the expression of genes, such as SOX-9, type II collagen and aggrecan, in newly differentiated cells by real-time PCR (qRT-PCR). The production of type II collagen protein was observed by western blotting. Immunohistochemistry analysis was also performed to detect collagen type II and aggrecan. This study was approved by the local ethics committee. RESULTS: SOX-9, aggrecan and type II collagen were expressed in newly differentiated chondrocytes. The expression of SOX-9 was significantly higher in newly differentiated chondrocytes than in adult cartilage. Collagen type II protein was also detected. CONCLUSION: We demonstrate that stem cells from human amniotic fluid are a suitable source for chondrogenesis when cultured in a micromass system. amniotic fluid mesenchymal stromal stem cells are an extremely viable source for clinical applications, and our results suggest the possibility of using human amniotic fluid as a source of mesenchymal stem cells.
publishDate 2018
dc.date.none.fl_str_mv 2018-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/146255
10.6061/clinics/2018/e268
url https://www.revistas.usp.br/clinics/article/view/146255
identifier_str_mv 10.6061/clinics/2018/e268
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/146255/139944
dc.rights.driver.fl_str_mv Copyright (c) 2018 Clinics
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2018 Clinics
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 73 (2018); e268
Clinics; v. 73 (2018); e268
Clinics; Vol. 73 (2018); e268
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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