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Data from ameloblast cell lines cultured in 3D using various gel substrates in the presence of ameloblastin

This article contains data related to the research article in this issue titled ameloblastin promotes polarization of ameloblast cell lines in a 3D cell culture system (Visakan et al., 2022). In the process of amelogenesis, the organic matrix components are pivotal to the establishment of ameloblast...

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Autores principales: Visakan, Gayathri, Su, Jingtan, Moradian-Oldak, Janet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9108880/
https://www.ncbi.nlm.nih.gov/pubmed/35586397
http://dx.doi.org/10.1016/j.dib.2022.108233
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author Visakan, Gayathri
Su, Jingtan
Moradian-Oldak, Janet
author_facet Visakan, Gayathri
Su, Jingtan
Moradian-Oldak, Janet
author_sort Visakan, Gayathri
collection PubMed
description This article contains data related to the research article in this issue titled ameloblastin promotes polarization of ameloblast cell lines in a 3D cell culture system (Visakan et al., 2022). In the process of amelogenesis, the organic matrix components are pivotal to the establishment of ameloblast-matrix adhesion. Here we employ immortalized ameloblast cell lines and analyse their morphological changes in 3D cell culture when cultured in the presence of recombinant enamel matrix proteins- ameloblastin and amelogenin compared with controls. The recombinant proteins that were purified using high-performance liquid chromatography (HPLC) were characterized using SDS-gel electrophoresis. A 3D-on-top culture technique was employed, and the cells were analysed 24 and 72 h post inoculation using fluorescent and confocal microscopy for qualitative and quantitative changes. Aspect ratio of cells was measured and used as the parameter to compare between test proteins and controls. Repeated measurements of aspect ratio were recorded to analyse for statistical significance. Additionally, three distinct gel substrates were studied to examine the effect of composition and stiffness of the substrate on cell behaviour. The cells in the 3D culture were fixed and labelled using antibodies to junctional complex, polarity and tight junctional proteins following protocols for whole culture fixation. Co-localization between membrane and specific antibody labels were examined under confocal microscopy.
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spelling pubmed-91088802022-05-17 Data from ameloblast cell lines cultured in 3D using various gel substrates in the presence of ameloblastin Visakan, Gayathri Su, Jingtan Moradian-Oldak, Janet Data Brief Data Article This article contains data related to the research article in this issue titled ameloblastin promotes polarization of ameloblast cell lines in a 3D cell culture system (Visakan et al., 2022). In the process of amelogenesis, the organic matrix components are pivotal to the establishment of ameloblast-matrix adhesion. Here we employ immortalized ameloblast cell lines and analyse their morphological changes in 3D cell culture when cultured in the presence of recombinant enamel matrix proteins- ameloblastin and amelogenin compared with controls. The recombinant proteins that were purified using high-performance liquid chromatography (HPLC) were characterized using SDS-gel electrophoresis. A 3D-on-top culture technique was employed, and the cells were analysed 24 and 72 h post inoculation using fluorescent and confocal microscopy for qualitative and quantitative changes. Aspect ratio of cells was measured and used as the parameter to compare between test proteins and controls. Repeated measurements of aspect ratio were recorded to analyse for statistical significance. Additionally, three distinct gel substrates were studied to examine the effect of composition and stiffness of the substrate on cell behaviour. The cells in the 3D culture were fixed and labelled using antibodies to junctional complex, polarity and tight junctional proteins following protocols for whole culture fixation. Co-localization between membrane and specific antibody labels were examined under confocal microscopy. Elsevier 2022-05-05 /pmc/articles/PMC9108880/ /pubmed/35586397 http://dx.doi.org/10.1016/j.dib.2022.108233 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Data Article
Visakan, Gayathri
Su, Jingtan
Moradian-Oldak, Janet
Data from ameloblast cell lines cultured in 3D using various gel substrates in the presence of ameloblastin
title Data from ameloblast cell lines cultured in 3D using various gel substrates in the presence of ameloblastin
title_full Data from ameloblast cell lines cultured in 3D using various gel substrates in the presence of ameloblastin
title_fullStr Data from ameloblast cell lines cultured in 3D using various gel substrates in the presence of ameloblastin
title_full_unstemmed Data from ameloblast cell lines cultured in 3D using various gel substrates in the presence of ameloblastin
title_short Data from ameloblast cell lines cultured in 3D using various gel substrates in the presence of ameloblastin
title_sort data from ameloblast cell lines cultured in 3d using various gel substrates in the presence of ameloblastin
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9108880/
https://www.ncbi.nlm.nih.gov/pubmed/35586397
http://dx.doi.org/10.1016/j.dib.2022.108233
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