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A novel role of sesamol in inhibiting NF-κB-mediated signaling in platelet activation

BACKGROUND: Platelet activation is relevant to a variety of coronary heart diseases. Our previous studies revealed that sesamol possesses potent antiplatelet activity through increasing cyclic AMP formation. Although platelets are anucleated cells, they also express the transcription factor, NF-κB,...

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Autores principales: Chang, Chao-Chien, Lu, Wan-Jung, Ong, Eng-Thiam, Chiang, Cheng-Wen, Lin, Song-Chow, Huang, Shih-Yi, Sheu, Joen-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258208/
https://www.ncbi.nlm.nih.gov/pubmed/22168157
http://dx.doi.org/10.1186/1423-0127-18-93
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author Chang, Chao-Chien
Lu, Wan-Jung
Ong, Eng-Thiam
Chiang, Cheng-Wen
Lin, Song-Chow
Huang, Shih-Yi
Sheu, Joen-Rong
author_facet Chang, Chao-Chien
Lu, Wan-Jung
Ong, Eng-Thiam
Chiang, Cheng-Wen
Lin, Song-Chow
Huang, Shih-Yi
Sheu, Joen-Rong
author_sort Chang, Chao-Chien
collection PubMed
description BACKGROUND: Platelet activation is relevant to a variety of coronary heart diseases. Our previous studies revealed that sesamol possesses potent antiplatelet activity through increasing cyclic AMP formation. Although platelets are anucleated cells, they also express the transcription factor, NF-κB, that may exert non-genomic functions in platelet activation. Therefore, we further investigated the inhibitory roles of sesamol in NF-κB-mediated platelet function. METHODS: Platelet aggregation, Fura 2-AM fluorescence, and immunoblotting analysis were used in this study. RESULTS: NF-κB signaling events, including IKKβ phosphorylation, IκBα degradation, and p65 phosphorylation, were markedly activated by collagen (1 μg/ml) in washed human platelets, and these signaling events were attenuated by sesamol (2.5~25 μM). Furthermore, SQ22536 and ODQ, inhibitors of adenylate cyclase and guanylate cyclase, respectively, strongly reversed the sesamol (25 μM)-mediated inhibitory effects of IKKβ phosphorylation, IκBα degradation, and p65 phosphorylation stimulated by collagen. The protein kinase A (PKA) inhibitor, H89, also reversed sesamol-mediated inhibition of IκBα degradation. Moreover, BAY11-7082, an NF-κB inhibitor, abolished IκBα degradation, phospholipase C (PLC)γ2 phosphorylation, protein kinase C (PKC) activation, [Ca(2+)]i mobilization, and platelet aggregation stimulated by collagen. Preincubation of platelets with the inhibitors, SQ22536 and H89, both strongly reversed sesamol-mediated inhibition of platelet aggregation and [Ca(2+)]i mobilization. CONCLUSIONS: Sesamol activates cAMP-PKA signaling, followed by inhibition of the NF-κB-PLC-PKC cascade, thereby leading to inhibition of [Ca(2+)]i mobilization and platelet aggregation. Because platelet activation is not only linked to hemostasis, but also has a relevant role in inflammation and metastasis, our data demonstrating that inhibition of NF-κB interferes with platelet function may have a great impact when these types of drugs are considered for the treatment of cancer and various inflammatory diseases.
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spelling pubmed-32582082012-01-14 A novel role of sesamol in inhibiting NF-κB-mediated signaling in platelet activation Chang, Chao-Chien Lu, Wan-Jung Ong, Eng-Thiam Chiang, Cheng-Wen Lin, Song-Chow Huang, Shih-Yi Sheu, Joen-Rong J Biomed Sci Research BACKGROUND: Platelet activation is relevant to a variety of coronary heart diseases. Our previous studies revealed that sesamol possesses potent antiplatelet activity through increasing cyclic AMP formation. Although platelets are anucleated cells, they also express the transcription factor, NF-κB, that may exert non-genomic functions in platelet activation. Therefore, we further investigated the inhibitory roles of sesamol in NF-κB-mediated platelet function. METHODS: Platelet aggregation, Fura 2-AM fluorescence, and immunoblotting analysis were used in this study. RESULTS: NF-κB signaling events, including IKKβ phosphorylation, IκBα degradation, and p65 phosphorylation, were markedly activated by collagen (1 μg/ml) in washed human platelets, and these signaling events were attenuated by sesamol (2.5~25 μM). Furthermore, SQ22536 and ODQ, inhibitors of adenylate cyclase and guanylate cyclase, respectively, strongly reversed the sesamol (25 μM)-mediated inhibitory effects of IKKβ phosphorylation, IκBα degradation, and p65 phosphorylation stimulated by collagen. The protein kinase A (PKA) inhibitor, H89, also reversed sesamol-mediated inhibition of IκBα degradation. Moreover, BAY11-7082, an NF-κB inhibitor, abolished IκBα degradation, phospholipase C (PLC)γ2 phosphorylation, protein kinase C (PKC) activation, [Ca(2+)]i mobilization, and platelet aggregation stimulated by collagen. Preincubation of platelets with the inhibitors, SQ22536 and H89, both strongly reversed sesamol-mediated inhibition of platelet aggregation and [Ca(2+)]i mobilization. CONCLUSIONS: Sesamol activates cAMP-PKA signaling, followed by inhibition of the NF-κB-PLC-PKC cascade, thereby leading to inhibition of [Ca(2+)]i mobilization and platelet aggregation. Because platelet activation is not only linked to hemostasis, but also has a relevant role in inflammation and metastasis, our data demonstrating that inhibition of NF-κB interferes with platelet function may have a great impact when these types of drugs are considered for the treatment of cancer and various inflammatory diseases. BioMed Central 2011-12-14 /pmc/articles/PMC3258208/ /pubmed/22168157 http://dx.doi.org/10.1186/1423-0127-18-93 Text en Copyright ©2011 Chang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Chang, Chao-Chien
Lu, Wan-Jung
Ong, Eng-Thiam
Chiang, Cheng-Wen
Lin, Song-Chow
Huang, Shih-Yi
Sheu, Joen-Rong
A novel role of sesamol in inhibiting NF-κB-mediated signaling in platelet activation
title A novel role of sesamol in inhibiting NF-κB-mediated signaling in platelet activation
title_full A novel role of sesamol in inhibiting NF-κB-mediated signaling in platelet activation
title_fullStr A novel role of sesamol in inhibiting NF-κB-mediated signaling in platelet activation
title_full_unstemmed A novel role of sesamol in inhibiting NF-κB-mediated signaling in platelet activation
title_short A novel role of sesamol in inhibiting NF-κB-mediated signaling in platelet activation
title_sort novel role of sesamol in inhibiting nf-κb-mediated signaling in platelet activation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3258208/
https://www.ncbi.nlm.nih.gov/pubmed/22168157
http://dx.doi.org/10.1186/1423-0127-18-93
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