Primary culture of fibrocondrocytes from rabbit knee joint meniscus
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Publication Date: | 2005 |
Other Authors: | |
Format: | Article |
Language: | por |
Source: | Revista do Instituto Adolfo Lutz (Online) |
Download full: | https://periodicos.saude.sp.gov.br/RIAL/article/view/32994 |
Summary: | The present study describes a primary culture of meniscus fibrocartilaginous tissue cultivated in high density technique. Cells were isolated from menisci fibrocartilaginous from 120 days-old New Zealand white rabbits. Menisci were finely minced , and treated with 2mg/mL collagenase in DMEM (Dulbecco's modified Eagle's medium) containing 10% FSC (fetal calf serum) in a shaker for three hours at 37ºC. Fibrochondrocyte cells were seeded at high density (1x105 cells /cm2) in T25 flasks containing DMEM supplemented with 10% FCS. Nearly 80% of cells attached to the flask , and after culturing for five days the cells were uniformly displayed as an elongated, fibroblastic-like morphology. The cells showed confluence after approximately 15 days of culture ,and produced sufficient extracellular matrix which could be evidenced by the appearance of toluidine blue metachromasia. No morphological changes were observed in fibrochondrocytes during cells growing. The fibrochondrocytes cells growth rate increased 2.5 fold, and attained to the stationary phase. During seven days, the newly glycosaminglycans synthesizing cells, the rate of total synthesis of glycosaminglycan was high, and it remained stable after monolayer cells confluency. Ultrastructural morphology of monolayer cells after culturing for eight days was identical to typical fibrochondrocyte in vivo. |
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Primary culture of fibrocondrocytes from rabbit knee joint meniscusCultura primária de fibrocondrócitos de menisco de coelhocell culturemeniscifibrochondrocytescultura de célulameniscofibrocondrócitosThe present study describes a primary culture of meniscus fibrocartilaginous tissue cultivated in high density technique. Cells were isolated from menisci fibrocartilaginous from 120 days-old New Zealand white rabbits. Menisci were finely minced , and treated with 2mg/mL collagenase in DMEM (Dulbecco's modified Eagle's medium) containing 10% FSC (fetal calf serum) in a shaker for three hours at 37ºC. Fibrochondrocyte cells were seeded at high density (1x105 cells /cm2) in T25 flasks containing DMEM supplemented with 10% FCS. Nearly 80% of cells attached to the flask , and after culturing for five days the cells were uniformly displayed as an elongated, fibroblastic-like morphology. The cells showed confluence after approximately 15 days of culture ,and produced sufficient extracellular matrix which could be evidenced by the appearance of toluidine blue metachromasia. No morphological changes were observed in fibrochondrocytes during cells growing. The fibrochondrocytes cells growth rate increased 2.5 fold, and attained to the stationary phase. During seven days, the newly glycosaminglycans synthesizing cells, the rate of total synthesis of glycosaminglycan was high, and it remained stable after monolayer cells confluency. Ultrastructural morphology of monolayer cells after culturing for eight days was identical to typical fibrochondrocyte in vivo.Estudos envolvendo a obtenção de fibrocondrócitos em cultura no Brasil são escassos. Este trabalho descreve a cultura primária de fibrocondrócitos de menisco cultivados em alta densidade com algumas modificações nos métodos de extração já descritos na literatura, com o intuito de obter um maior número de células viáveis para cultivo celular. Foram utilizados meniscos de coelhos New Zealand com 120 dias. Os meniscos foram cortados e tratados com 2mg/ml de colagenase diluída em meio DMEM (meio de Eagle modificado por Dulbeccos) contendo 10% de SFB sob agitação durante três horas a 37ºC. Os fibrocondrócitos foram cultivados em alta densidade (1x105/cm2) em frascos de cultura T25 em meio DMEM suplementado com 10% de SFB. As células atingiram a confluência celular após o 15º dia de cultivo e sintetizaram sua matrix extracelular evidenciada pela coloração com azul de toluidina. A curva de crescimento mostrou que os fibrocondrócitos duplicaram 2,5 vezes. A cinética de incorporação de sulfato radioativo nos glicosaminoglicanos sintetizados pelos fibrocondrócitos "in vitro" foi constante. Os fibrocondrócitos cultivados em alta densidade celular apresentaram aspectos ultra-estruturais semelhante as células " in vivo".Instituto Adolfo Lutz2005-02-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAvaliado pelos paresapplication/pdfhttps://periodicos.saude.sp.gov.br/RIAL/article/view/3299410.53393/rial.2005.64.32994Instituto Adolfo Lutz Journal - RIAL; Vol. 64 No. 2 (2005); 263-268Revista del Instituto Adolfo Lutz - RIAL; Vol. 64 Núm. 2 (2005); 263-268Revista do Instituto Adolfo Lutz; v. 64 n. 2 (2005); 263-2681983-38140073-9855reponame:Revista do Instituto Adolfo Lutz (Online)instname:Instituto Adolfo Lutzinstacron:IALporhttps://periodicos.saude.sp.gov.br/RIAL/article/view/32994/31826Copyright (c) 2005 Cristina Adelaide Figueiredo, Paulo Pinto Joazeiroinfo:eu-repo/semantics/openAccessFigueiredo, Cristina AdelaideJoazeiro, Paulo Pinto2024-01-23T12:25:53Zoai:ojs.periodicos.saude.sp.gov.br:article/32994Revistahttps://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:2024-01-23T12:25:53Revista do Instituto Adolfo Lutz (Online) - Instituto Adolfo Lutzfalse |
dc.title.none.fl_str_mv |
Primary culture of fibrocondrocytes from rabbit knee joint meniscus Cultura primária de fibrocondrócitos de menisco de coelho |
title |
Primary culture of fibrocondrocytes from rabbit knee joint meniscus |
spellingShingle |
Primary culture of fibrocondrocytes from rabbit knee joint meniscus Figueiredo, Cristina Adelaide cell culture menisci fibrochondrocytes cultura de célula menisco fibrocondrócitos |
title_short |
Primary culture of fibrocondrocytes from rabbit knee joint meniscus |
title_full |
Primary culture of fibrocondrocytes from rabbit knee joint meniscus |
title_fullStr |
Primary culture of fibrocondrocytes from rabbit knee joint meniscus |
title_full_unstemmed |
Primary culture of fibrocondrocytes from rabbit knee joint meniscus |
title_sort |
Primary culture of fibrocondrocytes from rabbit knee joint meniscus |
author |
Figueiredo, Cristina Adelaide |
author_facet |
Figueiredo, Cristina Adelaide Joazeiro, Paulo Pinto |
author_role |
author |
author2 |
Joazeiro, Paulo Pinto |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Figueiredo, Cristina Adelaide Joazeiro, Paulo Pinto |
dc.subject.por.fl_str_mv |
cell culture menisci fibrochondrocytes cultura de célula menisco fibrocondrócitos |
topic |
cell culture menisci fibrochondrocytes cultura de célula menisco fibrocondrócitos |
description |
The present study describes a primary culture of meniscus fibrocartilaginous tissue cultivated in high density technique. Cells were isolated from menisci fibrocartilaginous from 120 days-old New Zealand white rabbits. Menisci were finely minced , and treated with 2mg/mL collagenase in DMEM (Dulbecco's modified Eagle's medium) containing 10% FSC (fetal calf serum) in a shaker for three hours at 37ºC. Fibrochondrocyte cells were seeded at high density (1x105 cells /cm2) in T25 flasks containing DMEM supplemented with 10% FCS. Nearly 80% of cells attached to the flask , and after culturing for five days the cells were uniformly displayed as an elongated, fibroblastic-like morphology. The cells showed confluence after approximately 15 days of culture ,and produced sufficient extracellular matrix which could be evidenced by the appearance of toluidine blue metachromasia. No morphological changes were observed in fibrochondrocytes during cells growing. The fibrochondrocytes cells growth rate increased 2.5 fold, and attained to the stationary phase. During seven days, the newly glycosaminglycans synthesizing cells, the rate of total synthesis of glycosaminglycan was high, and it remained stable after monolayer cells confluency. Ultrastructural morphology of monolayer cells after culturing for eight days was identical to typical fibrochondrocyte in vivo. |
publishDate |
2005 |
dc.date.none.fl_str_mv |
2005-02-10 |
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/32994 10.53393/rial.2005.64.32994 |
url |
https://periodicos.saude.sp.gov.br/RIAL/article/view/32994 |
identifier_str_mv |
10.53393/rial.2005.64.32994 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://periodicos.saude.sp.gov.br/RIAL/article/view/32994/31826 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2005 Cristina Adelaide Figueiredo, Paulo Pinto Joazeiro info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2005 Cristina Adelaide Figueiredo, Paulo Pinto Joazeiro |
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. 64 No. 2 (2005); 263-268 Revista del Instituto Adolfo Lutz - RIAL; Vol. 64 Núm. 2 (2005); 263-268 Revista do Instituto Adolfo Lutz; v. 64 n. 2 (2005); 263-268 1983-3814 0073-9855 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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1836991959040786432 |