Culture of human articular chondrocyte in monolayer

Bibliographic Details
Main Author: Kitadai, Fabio T.
Publication Date: 2003
Other Authors: Figueiredo, Cristina A., Curti, Suely P., Leme, Luis Eugênio G., Carelli, Clara D. R., Amatuzzi, Marco M.
Format: Article
Language: por
Source: Revista do Instituto Adolfo Lutz (Online)
Download full: https://periodicos.saude.sp.gov.br/RIAL/article/view/34903
Summary: The purpose of this study was the padronization of the obtained human articular cartilagecell culture methodology. Five patients were selected from Instituto de Ortopedia e Traumatologia do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (IOT-HC-FMUSP). All patients suffered from anterior ligament lesion with cartilage degeneration. The diagnosis and the surgery were performed by knee arthroscopy. The articular cartilage fragments (weight, 300 to 500 mg) mg were placed in Petri dishes containing Dulbecco´s modified Eagle´s medium (DMEM) with 40µg/ml. The fragment was finely diced and treated with 2mg/ml collagenase in medium DMEM containing 10% fetal serum bovine. The cells isolated were seeded at hight density in T25 flasks in medium DMEM with 10% offetal calf serum (FCS). The cells attached to the flask after 24 hours the cells began to adhere to the flask. By day 3 the cell culture presented elipsoid and star morphology. Cultures fixed and stained with toluidine blue showed extracellular staining, suggesting these cells had begun to synthesize a new matrix. The growth rate of chondrocytes was high in the 2nd and 3nd days of the cultive. The chondrocytes were frozen into liquid nitrogen and showed high viability...
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spelling Culture of human articular chondrocyte in monolayerCultura primária de condrócitos articular humana em monocamadacartilagechondrocytecell culturecartilagemcondrócitocultura celularThe purpose of this study was the padronization of the obtained human articular cartilagecell culture methodology. Five patients were selected from Instituto de Ortopedia e Traumatologia do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (IOT-HC-FMUSP). All patients suffered from anterior ligament lesion with cartilage degeneration. The diagnosis and the surgery were performed by knee arthroscopy. The articular cartilage fragments (weight, 300 to 500 mg) mg were placed in Petri dishes containing Dulbecco´s modified Eagle´s medium (DMEM) with 40µg/ml. The fragment was finely diced and treated with 2mg/ml collagenase in medium DMEM containing 10% fetal serum bovine. The cells isolated were seeded at hight density in T25 flasks in medium DMEM with 10% offetal calf serum (FCS). The cells attached to the flask after 24 hours the cells began to adhere to the flask. By day 3 the cell culture presented elipsoid and star morphology. Cultures fixed and stained with toluidine blue showed extracellular staining, suggesting these cells had begun to synthesize a new matrix. The growth rate of chondrocytes was high in the 2nd and 3nd days of the cultive. The chondrocytes were frozen into liquid nitrogen and showed high viability...O objetivo deste trabalho foi padronizar a metodologia para obtenção de cultura primária de condrócitos de cartilagem hialina articular humana para sua utilização em transplante autólogo. Foram selecionados cinco pacientes do Instituto de Ortopedia e Traumatologia do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (IOT-HC-FMUSP) sem doença degenerativa articular, com indicação de cirurgia artroscópica para correção de afecção do ligamento cruzado anterior do joelho. Os fragmentos de cartilagem articular pesando aproximadamente 300-500 mg foram colocados em placas de Petri contendo meio de Eagle modificado por Dulbecco´s (DMEM) com 40µg/ml de gentamicina. Cada fragmento foi cortado e colocado em 2mg/ml de colagenase diluída em meio DMEM com 10% de soro fetal bovino (SFB). As células foram isoladas e cultivadas em frasco de cultura T25 em meio DMEM suplementado com 10% de SFB. As células aderiram ao frasco de cultura após 24 h e após o 3° dia de cultivo as células apresentavam morfologia elipsóide e estrelada. As culturas foram fixadas e coradas intensamente com azul de toluidina sugerindo que as células iniciaram a síntese de uma nova matriz extracellular. A curva de crescimento mostrou que a razão de crescimento foi em torno do segundo e terceiro...Instituto Adolfo Lutz2003-12-30info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAvaliado pelos paresapplication/pdfhttps://periodicos.saude.sp.gov.br/RIAL/article/view/3490310.53393/rial.2003.62.34903Instituto Adolfo Lutz Journal - RIAL; Vol. 62 No. 3 (2003); 221-6Revista del Instituto Adolfo Lutz - RIAL; Vol. 62 Núm. 3 (2003); 221-6Revista do Instituto Adolfo Lutz; v. 62 n. 3 (2003); 221-61983-38140073-985510.18241/rial.v62i3reponame:Revista do Instituto Adolfo Lutz (Online)instname:Instituto Adolfo Lutzinstacron:IALporhttps://periodicos.saude.sp.gov.br/RIAL/article/view/34903/33406Copyright (c) 2003 Fabio T. Kitadai, Cristina A. Figueiredo, Suely P. Curti, Luis Eugênio G. Leme, Clara D. R. Carelli, Marco M. Amatuzziinfo:eu-repo/semantics/openAccessKitadai, Fabio T. Figueiredo, Cristina A. Curti, Suely P. Leme, Luis Eugênio G. Carelli, Clara D. R. Amatuzzi, Marco M. 2024-01-23T18:00:58Zoai:ojs.periodicos.saude.sp.gov.br:article/34903Revistahttps://periodicos.saude.sp.gov.br/RIAL/indexPUBhttps://periodicos.saude.sp.gov.br/RIAL/oairial@saude.sp.gov.brhttps://doi.org/10.53393/rial1983-38140073-9855opendoar:2024-01-23T18:00:58Revista do Instituto Adolfo Lutz (Online) - Instituto Adolfo Lutzfalse
dc.title.none.fl_str_mv Culture of human articular chondrocyte in monolayer
Cultura primária de condrócitos articular humana em monocamada
title Culture of human articular chondrocyte in monolayer
spellingShingle Culture of human articular chondrocyte in monolayer
Kitadai, Fabio T.
cartilage
chondrocyte
cell culture
cartilagem
condrócito
cultura celular
title_short Culture of human articular chondrocyte in monolayer
title_full Culture of human articular chondrocyte in monolayer
title_fullStr Culture of human articular chondrocyte in monolayer
title_full_unstemmed Culture of human articular chondrocyte in monolayer
title_sort Culture of human articular chondrocyte in monolayer
author Kitadai, Fabio T.
author_facet Kitadai, Fabio T.
Figueiredo, Cristina A.
Curti, Suely P.
Leme, Luis Eugênio G.
Carelli, Clara D. R.
Amatuzzi, Marco M.
author_role author
author2 Figueiredo, Cristina A.
Curti, Suely P.
Leme, Luis Eugênio G.
Carelli, Clara D. R.
Amatuzzi, Marco M.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Kitadai, Fabio T.
Figueiredo, Cristina A.
Curti, Suely P.
Leme, Luis Eugênio G.
Carelli, Clara D. R.
Amatuzzi, Marco M.
dc.subject.por.fl_str_mv cartilage
chondrocyte
cell culture
cartilagem
condrócito
cultura celular
topic cartilage
chondrocyte
cell culture
cartilagem
condrócito
cultura celular
description The purpose of this study was the padronization of the obtained human articular cartilagecell culture methodology. Five patients were selected from Instituto de Ortopedia e Traumatologia do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (IOT-HC-FMUSP). All patients suffered from anterior ligament lesion with cartilage degeneration. The diagnosis and the surgery were performed by knee arthroscopy. The articular cartilage fragments (weight, 300 to 500 mg) mg were placed in Petri dishes containing Dulbecco´s modified Eagle´s medium (DMEM) with 40µg/ml. The fragment was finely diced and treated with 2mg/ml collagenase in medium DMEM containing 10% fetal serum bovine. The cells isolated were seeded at hight density in T25 flasks in medium DMEM with 10% offetal calf serum (FCS). The cells attached to the flask after 24 hours the cells began to adhere to the flask. By day 3 the cell culture presented elipsoid and star morphology. Cultures fixed and stained with toluidine blue showed extracellular staining, suggesting these cells had begun to synthesize a new matrix. The growth rate of chondrocytes was high in the 2nd and 3nd days of the cultive. The chondrocytes were frozen into liquid nitrogen and showed high viability...
publishDate 2003
dc.date.none.fl_str_mv 2003-12-30
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Avaliado pelos pares
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://periodicos.saude.sp.gov.br/RIAL/article/view/34903
10.53393/rial.2003.62.34903
url https://periodicos.saude.sp.gov.br/RIAL/article/view/34903
identifier_str_mv 10.53393/rial.2003.62.34903
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://periodicos.saude.sp.gov.br/RIAL/article/view/34903/33406
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Instituto Adolfo Lutz
publisher.none.fl_str_mv Instituto Adolfo Lutz
dc.source.none.fl_str_mv Instituto Adolfo Lutz Journal - RIAL; Vol. 62 No. 3 (2003); 221-6
Revista del Instituto Adolfo Lutz - RIAL; Vol. 62 Núm. 3 (2003); 221-6
Revista do Instituto Adolfo Lutz; v. 62 n. 3 (2003); 221-6
1983-3814
0073-9855
10.18241/rial.v62i3
reponame:Revista do Instituto Adolfo Lutz (Online)
instname:Instituto Adolfo Lutz
instacron:IAL
instname_str Instituto Adolfo Lutz
instacron_str IAL
institution IAL
reponame_str Revista do Instituto Adolfo Lutz (Online)
collection Revista do Instituto Adolfo Lutz (Online)
repository.name.fl_str_mv Revista do Instituto Adolfo Lutz (Online) - Instituto Adolfo Lutz
repository.mail.fl_str_mv rial@saude.sp.gov.br
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