Primary culture of fibrocondrocytes from rabbit knee joint meniscus

Bibliographic Details
Main Author: Figueiredo, Cristina Adelaide
Publication Date: 2005
Other Authors: Joazeiro, Paulo Pinto
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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spelling 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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