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Respective optimal calcium concentrations for proliferation on type I collagen fibrils in two keratinocyte line cells, HaCaT and FEPE1L-8

Keratinocyte line cells HaCaT and FEPE1L-8 are used for skin model with type I collagen fibrils (gels). For this purpose, not only differentiation but also regulation of proliferation on type I collagen gels by exogenous calcium concentration is important. When exogenous calcium concentration is low...

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Autores principales: Fujisaki, Hitomi, Futaki, Sugiko, Yamada, Masashi, Sekiguchi, Kiyotoshi, Hayashi, Toshihiko, Ikejima, Takashi, Hattori, Shunji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146901/
https://www.ncbi.nlm.nih.gov/pubmed/30271869
http://dx.doi.org/10.1016/j.reth.2018.04.001
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author Fujisaki, Hitomi
Futaki, Sugiko
Yamada, Masashi
Sekiguchi, Kiyotoshi
Hayashi, Toshihiko
Ikejima, Takashi
Hattori, Shunji
author_facet Fujisaki, Hitomi
Futaki, Sugiko
Yamada, Masashi
Sekiguchi, Kiyotoshi
Hayashi, Toshihiko
Ikejima, Takashi
Hattori, Shunji
author_sort Fujisaki, Hitomi
collection PubMed
description Keratinocyte line cells HaCaT and FEPE1L-8 are used for skin model with type I collagen fibrils (gels). For this purpose, not only differentiation but also regulation of proliferation on type I collagen gels by exogenous calcium concentration is important. When exogenous calcium concentration is low, primary keratinocyte proliferation is repressed and eventually cells are induced to apoptosis on type I collagen gels. The apoptosis induced on type I collagen gels is suppressed by increasing calcium concentration in the medium. That is, higher exogenous calcium concentration is necessary for primary keratinocyte survival on type I collagen gels than for that on dish surface culture. Meanwhile much higher exogenous calcium causes cell differentiation and inhibition of proliferation. The optimal calcium concentrations for proliferation on type I collagen gels have not been clarified in keratinocyte line cells. HaCaT cells have a unique calcium sensitivity in comparison with primary keratinocytes, whereas FEPE1L-8 cells have a similar sensitivity to primary keratinocytes. In this study, we compared the effect of calcium concentrations on proliferation of HaCaT and FEPE1L-8 cells on type I collagen gels. On type I collagen gels, both line cells required higher calcium concentrations for proliferation than on dish surface. HaCaT cells proliferated better in a wider range of calcium concentrations than FEPE1L-8 cells.
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spelling pubmed-61469012018-09-28 Respective optimal calcium concentrations for proliferation on type I collagen fibrils in two keratinocyte line cells, HaCaT and FEPE1L-8 Fujisaki, Hitomi Futaki, Sugiko Yamada, Masashi Sekiguchi, Kiyotoshi Hayashi, Toshihiko Ikejima, Takashi Hattori, Shunji Regen Ther Original Article Keratinocyte line cells HaCaT and FEPE1L-8 are used for skin model with type I collagen fibrils (gels). For this purpose, not only differentiation but also regulation of proliferation on type I collagen gels by exogenous calcium concentration is important. When exogenous calcium concentration is low, primary keratinocyte proliferation is repressed and eventually cells are induced to apoptosis on type I collagen gels. The apoptosis induced on type I collagen gels is suppressed by increasing calcium concentration in the medium. That is, higher exogenous calcium concentration is necessary for primary keratinocyte survival on type I collagen gels than for that on dish surface culture. Meanwhile much higher exogenous calcium causes cell differentiation and inhibition of proliferation. The optimal calcium concentrations for proliferation on type I collagen gels have not been clarified in keratinocyte line cells. HaCaT cells have a unique calcium sensitivity in comparison with primary keratinocytes, whereas FEPE1L-8 cells have a similar sensitivity to primary keratinocytes. In this study, we compared the effect of calcium concentrations on proliferation of HaCaT and FEPE1L-8 cells on type I collagen gels. On type I collagen gels, both line cells required higher calcium concentrations for proliferation than on dish surface. HaCaT cells proliferated better in a wider range of calcium concentrations than FEPE1L-8 cells. Japanese Society for Regenerative Medicine 2018-05-24 /pmc/articles/PMC6146901/ /pubmed/30271869 http://dx.doi.org/10.1016/j.reth.2018.04.001 Text en © 2018 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. http://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 Original Article
Fujisaki, Hitomi
Futaki, Sugiko
Yamada, Masashi
Sekiguchi, Kiyotoshi
Hayashi, Toshihiko
Ikejima, Takashi
Hattori, Shunji
Respective optimal calcium concentrations for proliferation on type I collagen fibrils in two keratinocyte line cells, HaCaT and FEPE1L-8
title Respective optimal calcium concentrations for proliferation on type I collagen fibrils in two keratinocyte line cells, HaCaT and FEPE1L-8
title_full Respective optimal calcium concentrations for proliferation on type I collagen fibrils in two keratinocyte line cells, HaCaT and FEPE1L-8
title_fullStr Respective optimal calcium concentrations for proliferation on type I collagen fibrils in two keratinocyte line cells, HaCaT and FEPE1L-8
title_full_unstemmed Respective optimal calcium concentrations for proliferation on type I collagen fibrils in two keratinocyte line cells, HaCaT and FEPE1L-8
title_short Respective optimal calcium concentrations for proliferation on type I collagen fibrils in two keratinocyte line cells, HaCaT and FEPE1L-8
title_sort respective optimal calcium concentrations for proliferation on type i collagen fibrils in two keratinocyte line cells, hacat and fepe1l-8
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146901/
https://www.ncbi.nlm.nih.gov/pubmed/30271869
http://dx.doi.org/10.1016/j.reth.2018.04.001
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