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Immunostimulatory Effects of Cordyceps militaris on Macrophages through the Enhanced Production of Cytokines via the Activation of NF-κB

BACKGROUND: Cordyceps militaris has been used in traditional medicine to treat numerous diseases and has been reported to possess both antitumor and immunomodulatory activities in vitro and in vivo. However, the pharmacological and biochemical mechanisms of Cordyceps militaris extract (CME) on macro...

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Autores principales: Shin, Seulmee, Kwon, Jeonghak, Lee, Sungwon, Kong, Hyunseok, Lee, Seungjeong, Lee, Chong-Kil, Cho, Kyunghae, Ha, Nam-Joo, Kim, Kyungjae
Formato: Texto
Lenguaje:English
Publicado: The Korean Association of Immunologists 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2881426/
https://www.ncbi.nlm.nih.gov/pubmed/20532125
http://dx.doi.org/10.4110/in.2010.10.2.55
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author Shin, Seulmee
Kwon, Jeonghak
Lee, Sungwon
Kong, Hyunseok
Lee, Seungjeong
Lee, Chong-Kil
Cho, Kyunghae
Ha, Nam-Joo
Kim, Kyungjae
author_facet Shin, Seulmee
Kwon, Jeonghak
Lee, Sungwon
Kong, Hyunseok
Lee, Seungjeong
Lee, Chong-Kil
Cho, Kyunghae
Ha, Nam-Joo
Kim, Kyungjae
author_sort Shin, Seulmee
collection PubMed
description BACKGROUND: Cordyceps militaris has been used in traditional medicine to treat numerous diseases and has been reported to possess both antitumor and immunomodulatory activities in vitro and in vivo. However, the pharmacological and biochemical mechanisms of Cordyceps militaris extract (CME) on macrophages have not been clearly elucidated. In the present study, we examined how CME induces the production of proinflammatory cytokines, transcription factor, and the expression of co-stimulatory molecules. METHODS: We confirmed the mRNA and protein levels of proinflammatory cytokines through RT-PCR and western blot analysis, followed by a FACS analysis for surface molecules. RESULTS: CME dose dependently increased the production of NO and proinflammatory cytokines such as IL-1β, IL-6, TNF-α, and PGE(2), and it induced the protein levels of iNOS, COX-2, and proinflammatory cytokines in a concentration-dependent manner, as determined by western blot and RT-PCR analysis, respectively. The expression of co-stimulatory molecules such as ICAM-1, B7-1, and B7-2 was also enhanced by CME. Furthermore, the activation of the nuclear transcription factor, NF-κB in macrophages was stimulated by CME. CONCLUSION: Based on these observations, CME increased proinflammatory cytokines through the activation of NF-κB, further suggesting that CME may prove useful as an immune-enhancing agent in the treatment of immunological disease.
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spelling pubmed-28814262010-06-07 Immunostimulatory Effects of Cordyceps militaris on Macrophages through the Enhanced Production of Cytokines via the Activation of NF-κB Shin, Seulmee Kwon, Jeonghak Lee, Sungwon Kong, Hyunseok Lee, Seungjeong Lee, Chong-Kil Cho, Kyunghae Ha, Nam-Joo Kim, Kyungjae Immune Netw Original Article BACKGROUND: Cordyceps militaris has been used in traditional medicine to treat numerous diseases and has been reported to possess both antitumor and immunomodulatory activities in vitro and in vivo. However, the pharmacological and biochemical mechanisms of Cordyceps militaris extract (CME) on macrophages have not been clearly elucidated. In the present study, we examined how CME induces the production of proinflammatory cytokines, transcription factor, and the expression of co-stimulatory molecules. METHODS: We confirmed the mRNA and protein levels of proinflammatory cytokines through RT-PCR and western blot analysis, followed by a FACS analysis for surface molecules. RESULTS: CME dose dependently increased the production of NO and proinflammatory cytokines such as IL-1β, IL-6, TNF-α, and PGE(2), and it induced the protein levels of iNOS, COX-2, and proinflammatory cytokines in a concentration-dependent manner, as determined by western blot and RT-PCR analysis, respectively. The expression of co-stimulatory molecules such as ICAM-1, B7-1, and B7-2 was also enhanced by CME. Furthermore, the activation of the nuclear transcription factor, NF-κB in macrophages was stimulated by CME. CONCLUSION: Based on these observations, CME increased proinflammatory cytokines through the activation of NF-κB, further suggesting that CME may prove useful as an immune-enhancing agent in the treatment of immunological disease. The Korean Association of Immunologists 2010-04 2010-04-30 /pmc/articles/PMC2881426/ /pubmed/20532125 http://dx.doi.org/10.4110/in.2010.10.2.55 Text en Copyright © 2010 The Korean Association of Immunologists 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 Original Article
Shin, Seulmee
Kwon, Jeonghak
Lee, Sungwon
Kong, Hyunseok
Lee, Seungjeong
Lee, Chong-Kil
Cho, Kyunghae
Ha, Nam-Joo
Kim, Kyungjae
Immunostimulatory Effects of Cordyceps militaris on Macrophages through the Enhanced Production of Cytokines via the Activation of NF-κB
title Immunostimulatory Effects of Cordyceps militaris on Macrophages through the Enhanced Production of Cytokines via the Activation of NF-κB
title_full Immunostimulatory Effects of Cordyceps militaris on Macrophages through the Enhanced Production of Cytokines via the Activation of NF-κB
title_fullStr Immunostimulatory Effects of Cordyceps militaris on Macrophages through the Enhanced Production of Cytokines via the Activation of NF-κB
title_full_unstemmed Immunostimulatory Effects of Cordyceps militaris on Macrophages through the Enhanced Production of Cytokines via the Activation of NF-κB
title_short Immunostimulatory Effects of Cordyceps militaris on Macrophages through the Enhanced Production of Cytokines via the Activation of NF-κB
title_sort immunostimulatory effects of cordyceps militaris on macrophages through the enhanced production of cytokines via the activation of nf-κb
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2881426/
https://www.ncbi.nlm.nih.gov/pubmed/20532125
http://dx.doi.org/10.4110/in.2010.10.2.55
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