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Serum-Induced Keratinization Processes in an Immortalized Human Meibomian Gland Epithelial Cell Line
PURPOSE: The aim of this study was to evaluate a human meibomian gland epithelial cell line (HMGEC) as a model for meibomian gland (patho)physiology in vitro. METHODS: HMGEC were cultured in the absence or presence of serum. Sudan III lipid staining, ultrastructural analysis and lipidomic analyses w...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456149/ https://www.ncbi.nlm.nih.gov/pubmed/26042605 http://dx.doi.org/10.1371/journal.pone.0128096 |
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author | Hampel, Ulrike Schröder, Antje Mitchell, Todd Brown, Simon Snikeris, Peta Garreis, Fabian Kunnen, Carolina Willcox, Mark Paulsen, Friedrich |
author_facet | Hampel, Ulrike Schröder, Antje Mitchell, Todd Brown, Simon Snikeris, Peta Garreis, Fabian Kunnen, Carolina Willcox, Mark Paulsen, Friedrich |
author_sort | Hampel, Ulrike |
collection | PubMed |
description | PURPOSE: The aim of this study was to evaluate a human meibomian gland epithelial cell line (HMGEC) as a model for meibomian gland (patho)physiology in vitro. METHODS: HMGEC were cultured in the absence or presence of serum. Sudan III lipid staining, ultrastructural analysis and lipidomic analyses were performed. Impedance sensing, desmoplakin 1/2 mRNA and cytokeratin (CK) 1, 5, 6, 14 levels were evaluated. Serum containing medium supplemented with higher serum, glucose, an omega-3 lipid cocktail, eicosapentaenoic acid or sebomed medium were investigated for lipid accumulation and ultrastructural morphology. RESULTS: Lipid droplet accumulation in HMGEC was induced by serum containing media after 1 day, but decreased over time. Cultivation in serum induced desmosome and cytokeratin filament formation. Desmoplakin 1/2 gene levels were significantly upregulated after 1d of serum treatment. Furthermore, the normalized impedance increased significantly. Lipidome analysis revealed high levels of phospholipids (over 50%), but very low levels of wax ester and cholesteryl esters (under 1%). Stimulation with eicosapentaenoic acid increased lipid accumulation after one day. CONCLUSION: Serum treatment of HMGEC caused lipid droplet formation to some extent but also induced keratinization. The cells did not produce typical meibum lipids under these growth conditions. HMGEC are well suited to study (hyper)keratinization processes of meibomian gland epithelial cells in vitro. |
format | Online Article Text |
id | pubmed-4456149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44561492015-06-09 Serum-Induced Keratinization Processes in an Immortalized Human Meibomian Gland Epithelial Cell Line Hampel, Ulrike Schröder, Antje Mitchell, Todd Brown, Simon Snikeris, Peta Garreis, Fabian Kunnen, Carolina Willcox, Mark Paulsen, Friedrich PLoS One Research Article PURPOSE: The aim of this study was to evaluate a human meibomian gland epithelial cell line (HMGEC) as a model for meibomian gland (patho)physiology in vitro. METHODS: HMGEC were cultured in the absence or presence of serum. Sudan III lipid staining, ultrastructural analysis and lipidomic analyses were performed. Impedance sensing, desmoplakin 1/2 mRNA and cytokeratin (CK) 1, 5, 6, 14 levels were evaluated. Serum containing medium supplemented with higher serum, glucose, an omega-3 lipid cocktail, eicosapentaenoic acid or sebomed medium were investigated for lipid accumulation and ultrastructural morphology. RESULTS: Lipid droplet accumulation in HMGEC was induced by serum containing media after 1 day, but decreased over time. Cultivation in serum induced desmosome and cytokeratin filament formation. Desmoplakin 1/2 gene levels were significantly upregulated after 1d of serum treatment. Furthermore, the normalized impedance increased significantly. Lipidome analysis revealed high levels of phospholipids (over 50%), but very low levels of wax ester and cholesteryl esters (under 1%). Stimulation with eicosapentaenoic acid increased lipid accumulation after one day. CONCLUSION: Serum treatment of HMGEC caused lipid droplet formation to some extent but also induced keratinization. The cells did not produce typical meibum lipids under these growth conditions. HMGEC are well suited to study (hyper)keratinization processes of meibomian gland epithelial cells in vitro. Public Library of Science 2015-06-04 /pmc/articles/PMC4456149/ /pubmed/26042605 http://dx.doi.org/10.1371/journal.pone.0128096 Text en © 2015 Hampel et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hampel, Ulrike Schröder, Antje Mitchell, Todd Brown, Simon Snikeris, Peta Garreis, Fabian Kunnen, Carolina Willcox, Mark Paulsen, Friedrich Serum-Induced Keratinization Processes in an Immortalized Human Meibomian Gland Epithelial Cell Line |
title | Serum-Induced Keratinization Processes in an Immortalized Human Meibomian Gland Epithelial Cell Line |
title_full | Serum-Induced Keratinization Processes in an Immortalized Human Meibomian Gland Epithelial Cell Line |
title_fullStr | Serum-Induced Keratinization Processes in an Immortalized Human Meibomian Gland Epithelial Cell Line |
title_full_unstemmed | Serum-Induced Keratinization Processes in an Immortalized Human Meibomian Gland Epithelial Cell Line |
title_short | Serum-Induced Keratinization Processes in an Immortalized Human Meibomian Gland Epithelial Cell Line |
title_sort | serum-induced keratinization processes in an immortalized human meibomian gland epithelial cell line |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4456149/ https://www.ncbi.nlm.nih.gov/pubmed/26042605 http://dx.doi.org/10.1371/journal.pone.0128096 |
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