Cargando…

Herbal extracts that induce type I interferons through Toll-like receptor 4 signaling

BACKGROUND: A mixture of five herbal extracts called internatural (INT), which is prepared from pumpkin seeds, purple turmeric, pearl barley, corn pistil, and cinnamon, is widely used by people in Japan and elsewhere for its immunity-enhancing effects and general health. Although anecdotal evidence...

Descripción completa

Detalles Bibliográficos
Autores principales: Nakasuji-Togi, Misa, Togi, Sumihito, Saeki, Keita, Kojima, Yasuhiko, Ozato, Keiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Open Academia 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809074/
https://www.ncbi.nlm.nih.gov/pubmed/35173566
http://dx.doi.org/10.29219/fnr.v66.5524
_version_ 1784643948058247168
author Nakasuji-Togi, Misa
Togi, Sumihito
Saeki, Keita
Kojima, Yasuhiko
Ozato, Keiko
author_facet Nakasuji-Togi, Misa
Togi, Sumihito
Saeki, Keita
Kojima, Yasuhiko
Ozato, Keiko
author_sort Nakasuji-Togi, Misa
collection PubMed
description BACKGROUND: A mixture of five herbal extracts called internatural (INT), which is prepared from pumpkin seeds, purple turmeric, pearl barley, corn pistil, and cinnamon, is widely used by people in Japan and elsewhere for its immunity-enhancing effects and general health. Although anecdotal evidence indicates its efficacy, the mechanisms by which INT boosts immunity have remained unknown. OBJECTIVE: The aim of this study was to investigate whether INT induces type I interferons (IFNs) in murine bone marrow-derived macrophages (BMDMs) and by what mechanism. DESIGN: We measured induction of type I IFNs (IFNβ and IFNα) in BMDMs treated with INT or other Toll-like receptor ligands: bacterial lipopolysaccharides (LPS), dsRNA, poly(I:C), and CpG oligonucleotides. To investigate whether INT signals through Toll-like receptor 4 (TLR4), we tested TLR4-specific inhibitor. We also tested if INT utilizes TLR4 adaptors, toll/IL-1 receptor (TIR) domain-containing adaptor (TRIF), or myeloid differentiation factor 88 (MyD88), we examined INT induction of IFNβ in TRIF-KO and MyD88-KO BMDMs. We then investigated whether INT provides an antiviral effect upon fibroblasts either directly or indirectly using the encephalomyocarditis virus (EMCV) model. RESULTS: We first observed that INT, when added to BMDMs, potently induces type I IFNs (IFNβ and IFNα) within 2 h. INT induction of IFN expression was mediated by TLR4, which signaled through the TRIF/MyD88 adaptors, similar to LPS. A high-molecular-weight fraction (MW > 10,000) of INT extracts contained IFN-inducing activity. Supernatants from INT-treated BMDMs protected untreated fibroblast from EMCV infection as reduced viral titers. CONCLUSIONS: INT induced type I IFN mRNA and proteins in BMDMs and other cell types. This induction was mediated by TLR4, which transduces signals using the TRIF/MyD88 pathway. The high-MW component of INT contained type I IFN inducing activity. The supernatants from INT-treated cells displayed antiviral activity and protected cells from EMCV infection. These findings indicate that INT is a novel natural IFN inducer that strengthens host’s innate immunity.
format Online
Article
Text
id pubmed-8809074
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Open Academia
record_format MEDLINE/PubMed
spelling pubmed-88090742022-02-15 Herbal extracts that induce type I interferons through Toll-like receptor 4 signaling Nakasuji-Togi, Misa Togi, Sumihito Saeki, Keita Kojima, Yasuhiko Ozato, Keiko Food Nutr Res Original Article BACKGROUND: A mixture of five herbal extracts called internatural (INT), which is prepared from pumpkin seeds, purple turmeric, pearl barley, corn pistil, and cinnamon, is widely used by people in Japan and elsewhere for its immunity-enhancing effects and general health. Although anecdotal evidence indicates its efficacy, the mechanisms by which INT boosts immunity have remained unknown. OBJECTIVE: The aim of this study was to investigate whether INT induces type I interferons (IFNs) in murine bone marrow-derived macrophages (BMDMs) and by what mechanism. DESIGN: We measured induction of type I IFNs (IFNβ and IFNα) in BMDMs treated with INT or other Toll-like receptor ligands: bacterial lipopolysaccharides (LPS), dsRNA, poly(I:C), and CpG oligonucleotides. To investigate whether INT signals through Toll-like receptor 4 (TLR4), we tested TLR4-specific inhibitor. We also tested if INT utilizes TLR4 adaptors, toll/IL-1 receptor (TIR) domain-containing adaptor (TRIF), or myeloid differentiation factor 88 (MyD88), we examined INT induction of IFNβ in TRIF-KO and MyD88-KO BMDMs. We then investigated whether INT provides an antiviral effect upon fibroblasts either directly or indirectly using the encephalomyocarditis virus (EMCV) model. RESULTS: We first observed that INT, when added to BMDMs, potently induces type I IFNs (IFNβ and IFNα) within 2 h. INT induction of IFN expression was mediated by TLR4, which signaled through the TRIF/MyD88 adaptors, similar to LPS. A high-molecular-weight fraction (MW > 10,000) of INT extracts contained IFN-inducing activity. Supernatants from INT-treated BMDMs protected untreated fibroblast from EMCV infection as reduced viral titers. CONCLUSIONS: INT induced type I IFN mRNA and proteins in BMDMs and other cell types. This induction was mediated by TLR4, which transduces signals using the TRIF/MyD88 pathway. The high-MW component of INT contained type I IFN inducing activity. The supernatants from INT-treated cells displayed antiviral activity and protected cells from EMCV infection. These findings indicate that INT is a novel natural IFN inducer that strengthens host’s innate immunity. Open Academia 2022-01-28 /pmc/articles/PMC8809074/ /pubmed/35173566 http://dx.doi.org/10.29219/fnr.v66.5524 Text en © 2022 Misa Nakasuji-Togi et al. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license.
spellingShingle Original Article
Nakasuji-Togi, Misa
Togi, Sumihito
Saeki, Keita
Kojima, Yasuhiko
Ozato, Keiko
Herbal extracts that induce type I interferons through Toll-like receptor 4 signaling
title Herbal extracts that induce type I interferons through Toll-like receptor 4 signaling
title_full Herbal extracts that induce type I interferons through Toll-like receptor 4 signaling
title_fullStr Herbal extracts that induce type I interferons through Toll-like receptor 4 signaling
title_full_unstemmed Herbal extracts that induce type I interferons through Toll-like receptor 4 signaling
title_short Herbal extracts that induce type I interferons through Toll-like receptor 4 signaling
title_sort herbal extracts that induce type i interferons through toll-like receptor 4 signaling
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809074/
https://www.ncbi.nlm.nih.gov/pubmed/35173566
http://dx.doi.org/10.29219/fnr.v66.5524
work_keys_str_mv AT nakasujitogimisa herbalextractsthatinducetypeiinterferonsthroughtolllikereceptor4signaling
AT togisumihito herbalextractsthatinducetypeiinterferonsthroughtolllikereceptor4signaling
AT saekikeita herbalextractsthatinducetypeiinterferonsthroughtolllikereceptor4signaling
AT kojimayasuhiko herbalextractsthatinducetypeiinterferonsthroughtolllikereceptor4signaling
AT ozatokeiko herbalextractsthatinducetypeiinterferonsthroughtolllikereceptor4signaling