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Immunostimulatory Effect of Laminarin on RAW 264.7 Mouse Macrophages

This study investigated the immunostimulatory effects of laminarin with respect to inflammatory mediators such as hydrogen peroxide, calcium, nitric oxide, various cytokines, transcription factors, and immune response gene in RAW 264.7 mouse macrophages. Laminarin did not reduce the cell proliferati...

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Detalles Bibliográficos
Autores principales: Lee, Ji Young, Kim, Young-Jin, Kim, Hyun Joo, Kim, Yoon-Sang, Park, Wansu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268557/
https://www.ncbi.nlm.nih.gov/pubmed/22569419
http://dx.doi.org/10.3390/molecules17055404
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author Lee, Ji Young
Kim, Young-Jin
Kim, Hyun Joo
Kim, Yoon-Sang
Park, Wansu
author_facet Lee, Ji Young
Kim, Young-Jin
Kim, Hyun Joo
Kim, Yoon-Sang
Park, Wansu
author_sort Lee, Ji Young
collection PubMed
description This study investigated the immunostimulatory effects of laminarin with respect to inflammatory mediators such as hydrogen peroxide, calcium, nitric oxide, various cytokines, transcription factors, and immune response gene in RAW 264.7 mouse macrophages. Laminarin did not reduce the cell proliferation of RAW 264.7 mouse macrophages at concentrations up to 500 µg/mL. Laminarin significantly increased the release of hydrogen peroxide, calcium, nitric oxide, monocyte chemotactic protein-1, vascular endothelial growth factor, leukemia inhibitory factor, and granulocyte-colony stimulating factor with enhancing expression of Signal Transducer and Activator of Transcription 1 (STAT1), STAT3, c-Jun, c-Fos, and cyclooxygenase-2 mRNA in RAW 264.7 cells. The results suggest that laminarin has immunostimulatory properties, strengthening immune reactions via the transcription factor pathway in macrophages.
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spelling pubmed-62685572018-12-20 Immunostimulatory Effect of Laminarin on RAW 264.7 Mouse Macrophages Lee, Ji Young Kim, Young-Jin Kim, Hyun Joo Kim, Yoon-Sang Park, Wansu Molecules Communication This study investigated the immunostimulatory effects of laminarin with respect to inflammatory mediators such as hydrogen peroxide, calcium, nitric oxide, various cytokines, transcription factors, and immune response gene in RAW 264.7 mouse macrophages. Laminarin did not reduce the cell proliferation of RAW 264.7 mouse macrophages at concentrations up to 500 µg/mL. Laminarin significantly increased the release of hydrogen peroxide, calcium, nitric oxide, monocyte chemotactic protein-1, vascular endothelial growth factor, leukemia inhibitory factor, and granulocyte-colony stimulating factor with enhancing expression of Signal Transducer and Activator of Transcription 1 (STAT1), STAT3, c-Jun, c-Fos, and cyclooxygenase-2 mRNA in RAW 264.7 cells. The results suggest that laminarin has immunostimulatory properties, strengthening immune reactions via the transcription factor pathway in macrophages. MDPI 2012-05-08 /pmc/articles/PMC6268557/ /pubmed/22569419 http://dx.doi.org/10.3390/molecules17055404 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Communication
Lee, Ji Young
Kim, Young-Jin
Kim, Hyun Joo
Kim, Yoon-Sang
Park, Wansu
Immunostimulatory Effect of Laminarin on RAW 264.7 Mouse Macrophages
title Immunostimulatory Effect of Laminarin on RAW 264.7 Mouse Macrophages
title_full Immunostimulatory Effect of Laminarin on RAW 264.7 Mouse Macrophages
title_fullStr Immunostimulatory Effect of Laminarin on RAW 264.7 Mouse Macrophages
title_full_unstemmed Immunostimulatory Effect of Laminarin on RAW 264.7 Mouse Macrophages
title_short Immunostimulatory Effect of Laminarin on RAW 264.7 Mouse Macrophages
title_sort immunostimulatory effect of laminarin on raw 264.7 mouse macrophages
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268557/
https://www.ncbi.nlm.nih.gov/pubmed/22569419
http://dx.doi.org/10.3390/molecules17055404
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