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Establishment and characterization of a canine sebaceous epithelial cell line derived from an eyelid mass
Little is known about the pathological roles of sebaceous glands in canine skin diseases, as most examinations have been conducted with cultured human sebaceous epithelial cell lines. To our knowledge, there is no available canine sebaceous epithelial cell line. The purpose of this study was to esta...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719885/ https://www.ncbi.nlm.nih.gov/pubmed/32921644 http://dx.doi.org/10.1292/jvms.20-0179 |
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author | MATSUDA, Akira MITSUI, Ikki SHIMIZU, Yuki KANDA, Teppei OHNISHI, Akihiro MIYABE, Masahiro ITOH, Yoshiki |
author_facet | MATSUDA, Akira MITSUI, Ikki SHIMIZU, Yuki KANDA, Teppei OHNISHI, Akihiro MIYABE, Masahiro ITOH, Yoshiki |
author_sort | MATSUDA, Akira |
collection | PubMed |
description | Little is known about the pathological roles of sebaceous glands in canine skin diseases, as most examinations have been conducted with cultured human sebaceous epithelial cell lines. To our knowledge, there is no available canine sebaceous epithelial cell line. The purpose of this study was to establish a canine sebaceous epithelial cell line and characterize it. An eyelid mass in a dog was surgically resected for treatment, and it was histologically diagnosed as sebaceous epithelioma. Collected tissue was conducted for culture, and the growing epithelial-like cells were passaged. The cells showed continuous proliferation for over 6 months. After 40 passages, the cells were named CMG-1. Lipid droplets in the cytoplasm of CMG-1 cells were confirmed by Oil Red O staining. As reported in studies with human sebaceous epithelial cell lines, lipogenesis in CMG-1 cells was promoted by linoleic acid, whereas transforming growth factor-β (TGF-β) suppressed it. Additionally, real-time PCR revealed that the expression levels of chemokines and cytokines, including CC chemokine ligand (CCL)-2, CCL-20, CXCL-10, Tumor necrosis factor-α (TNF-α), Interleukin (IL)-1α, IL-1β, and IL-8, were significantly increased in CMG-1 cells following treatment with lipopolysaccharide. In conclusion, we successfully established a new canine sebaceous epithelial cell line. Our data indicated that lipogenesis and inflammatory responses were quantitatively evaluable in this cell line. CMG-1 cells could be useful for the pathological analysis of sebaceous gland diseases in dogs. |
format | Online Article Text |
id | pubmed-7719885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-77198852020-12-09 Establishment and characterization of a canine sebaceous epithelial cell line derived from an eyelid mass MATSUDA, Akira MITSUI, Ikki SHIMIZU, Yuki KANDA, Teppei OHNISHI, Akihiro MIYABE, Masahiro ITOH, Yoshiki J Vet Med Sci Internal Medicine Little is known about the pathological roles of sebaceous glands in canine skin diseases, as most examinations have been conducted with cultured human sebaceous epithelial cell lines. To our knowledge, there is no available canine sebaceous epithelial cell line. The purpose of this study was to establish a canine sebaceous epithelial cell line and characterize it. An eyelid mass in a dog was surgically resected for treatment, and it was histologically diagnosed as sebaceous epithelioma. Collected tissue was conducted for culture, and the growing epithelial-like cells were passaged. The cells showed continuous proliferation for over 6 months. After 40 passages, the cells were named CMG-1. Lipid droplets in the cytoplasm of CMG-1 cells were confirmed by Oil Red O staining. As reported in studies with human sebaceous epithelial cell lines, lipogenesis in CMG-1 cells was promoted by linoleic acid, whereas transforming growth factor-β (TGF-β) suppressed it. Additionally, real-time PCR revealed that the expression levels of chemokines and cytokines, including CC chemokine ligand (CCL)-2, CCL-20, CXCL-10, Tumor necrosis factor-α (TNF-α), Interleukin (IL)-1α, IL-1β, and IL-8, were significantly increased in CMG-1 cells following treatment with lipopolysaccharide. In conclusion, we successfully established a new canine sebaceous epithelial cell line. Our data indicated that lipogenesis and inflammatory responses were quantitatively evaluable in this cell line. CMG-1 cells could be useful for the pathological analysis of sebaceous gland diseases in dogs. The Japanese Society of Veterinary Science 2020-09-11 2020-11 /pmc/articles/PMC7719885/ /pubmed/32921644 http://dx.doi.org/10.1292/jvms.20-0179 Text en ©2020 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Internal Medicine MATSUDA, Akira MITSUI, Ikki SHIMIZU, Yuki KANDA, Teppei OHNISHI, Akihiro MIYABE, Masahiro ITOH, Yoshiki Establishment and characterization of a canine sebaceous epithelial cell line derived from an eyelid mass |
title | Establishment and characterization of a canine sebaceous epithelial cell line derived from an eyelid mass |
title_full | Establishment and characterization of a canine sebaceous epithelial cell line derived from an eyelid mass |
title_fullStr | Establishment and characterization of a canine sebaceous epithelial cell line derived from an eyelid mass |
title_full_unstemmed | Establishment and characterization of a canine sebaceous epithelial cell line derived from an eyelid mass |
title_short | Establishment and characterization of a canine sebaceous epithelial cell line derived from an eyelid mass |
title_sort | establishment and characterization of a canine sebaceous epithelial cell line derived from an eyelid mass |
topic | Internal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7719885/ https://www.ncbi.nlm.nih.gov/pubmed/32921644 http://dx.doi.org/10.1292/jvms.20-0179 |
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