Culture of human articular chondrocyte in monolayer
Main Author: | |
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Publication Date: | 2003 |
Other Authors: | , , , , |
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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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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1836991962194903040 |