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In Vitro Immune-Enhancing Activity of Ovotransferrin from Egg White via MAPK Signaling Pathways in RAW 264.7 Macrophages
Ovotransferrin (OTF) is a well-known protein of the transferrin family with strong iron chelating activity, resulting in its antimicrobial activity. Furthermore, OTF is known to have antioxidant, anticancer, and antihypertensive activities. However, there have been few studies about the immune-enhan...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society for Food Science of Animal Resources
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335134/ https://www.ncbi.nlm.nih.gov/pubmed/30675115 http://dx.doi.org/10.5851/kosfa.2018.e56 |
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author | Lee, Jae Hoon Ahn, Dong Uk Paik, Hyun-Dong |
author_facet | Lee, Jae Hoon Ahn, Dong Uk Paik, Hyun-Dong |
author_sort | Lee, Jae Hoon |
collection | PubMed |
description | Ovotransferrin (OTF) is a well-known protein of the transferrin family with strong iron chelating activity, resulting in its antimicrobial activity. Furthermore, OTF is known to have antioxidant, anticancer, and antihypertensive activities. However, there have been few studies about the immune-enhancing activity of OTF. In current study, we investigated the immune-enhancing activity of OTF using the murine macrophage cells in vitro. The effect of OTF on production of pro-inflammatory mediators and cytokines were determined using Griess assay and quantitative real-time PCR. Using Neutral Red uptake assay, we confirmed the effect of OTF on phagocytic activity of macrophages. Ovotransferrin significantly increased the production of nitric oxide (NO) and secretion of inducible nitric oxide synthase (iNOS) mRNA with no cytotoxic activity. Ovotransferrin (2 mg/mL) stimulated NO production up to 31.9±3.5 μM. Ovotransferrin significantly increased the mRNA expression levels of pro-inflammatory cytokines which are tumor necrosis factor-α (TNF-α), Interleukin-1β (IL-1β), and IL-6: OTF (2 mg/mL) treatment increased the secretion of mRNA for TNF-α, IL-1β, and IL-6 by 22.20-, 37.91-, and 6.17-fold of the negative control, respectively. The phagocytic activity of macrophages was also increased by OTF treatment significantly compared with negative control. Also, OTF treatment increased phosphorylation level of MAPK signaling pathways. These results indicated that OTF has immune-enhancing activity by activating RAW 264.7 macrophages via MAPK pathways. |
format | Online Article Text |
id | pubmed-6335134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Korean Society for Food Science of Animal Resources |
record_format | MEDLINE/PubMed |
spelling | pubmed-63351342019-01-23 In Vitro Immune-Enhancing Activity of Ovotransferrin from Egg White via MAPK Signaling Pathways in RAW 264.7 Macrophages Lee, Jae Hoon Ahn, Dong Uk Paik, Hyun-Dong Korean J Food Sci Anim Resour Article Ovotransferrin (OTF) is a well-known protein of the transferrin family with strong iron chelating activity, resulting in its antimicrobial activity. Furthermore, OTF is known to have antioxidant, anticancer, and antihypertensive activities. However, there have been few studies about the immune-enhancing activity of OTF. In current study, we investigated the immune-enhancing activity of OTF using the murine macrophage cells in vitro. The effect of OTF on production of pro-inflammatory mediators and cytokines were determined using Griess assay and quantitative real-time PCR. Using Neutral Red uptake assay, we confirmed the effect of OTF on phagocytic activity of macrophages. Ovotransferrin significantly increased the production of nitric oxide (NO) and secretion of inducible nitric oxide synthase (iNOS) mRNA with no cytotoxic activity. Ovotransferrin (2 mg/mL) stimulated NO production up to 31.9±3.5 μM. Ovotransferrin significantly increased the mRNA expression levels of pro-inflammatory cytokines which are tumor necrosis factor-α (TNF-α), Interleukin-1β (IL-1β), and IL-6: OTF (2 mg/mL) treatment increased the secretion of mRNA for TNF-α, IL-1β, and IL-6 by 22.20-, 37.91-, and 6.17-fold of the negative control, respectively. The phagocytic activity of macrophages was also increased by OTF treatment significantly compared with negative control. Also, OTF treatment increased phosphorylation level of MAPK signaling pathways. These results indicated that OTF has immune-enhancing activity by activating RAW 264.7 macrophages via MAPK pathways. Korean Society for Food Science of Animal Resources 2018-12 2018-12-31 /pmc/articles/PMC6335134/ /pubmed/30675115 http://dx.doi.org/10.5851/kosfa.2018.e56 Text en © Copyright 2018 Korean Society for Food Science of Animal Resources http://creativecommons.org/licenses/by-nc/3.0/ This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Lee, Jae Hoon Ahn, Dong Uk Paik, Hyun-Dong In Vitro Immune-Enhancing Activity of Ovotransferrin from Egg White via MAPK Signaling Pathways in RAW 264.7 Macrophages |
title | In Vitro Immune-Enhancing Activity of Ovotransferrin
from Egg White via MAPK Signaling Pathways in RAW 264.7
Macrophages |
title_full | In Vitro Immune-Enhancing Activity of Ovotransferrin
from Egg White via MAPK Signaling Pathways in RAW 264.7
Macrophages |
title_fullStr | In Vitro Immune-Enhancing Activity of Ovotransferrin
from Egg White via MAPK Signaling Pathways in RAW 264.7
Macrophages |
title_full_unstemmed | In Vitro Immune-Enhancing Activity of Ovotransferrin
from Egg White via MAPK Signaling Pathways in RAW 264.7
Macrophages |
title_short | In Vitro Immune-Enhancing Activity of Ovotransferrin
from Egg White via MAPK Signaling Pathways in RAW 264.7
Macrophages |
title_sort | in vitro immune-enhancing activity of ovotransferrin
from egg white via mapk signaling pathways in raw 264.7
macrophages |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335134/ https://www.ncbi.nlm.nih.gov/pubmed/30675115 http://dx.doi.org/10.5851/kosfa.2018.e56 |
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