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      Wedelolactone facilitates Ser/Thr phosphorylation of NLRP3 dependent on PKA signalling to block inflammasome activation and pyroptosis

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          Abstract

          Objectives

          Wedelolactone exhibits regulatory effects on some inflammatory diseases. However, the anti‐inflammatory mechanism of wedelolactone has not been entirely unravelled. Therefore, the present study focuses on investigating the mechanism of wedelolactone on NLRP3 inflammasome in macrophages and its influence on MSU‐induced inflammation.

          Materials and Methods

          BMDM, J774A.1 and PMA‐differentiated THP‐1 macrophages were primed with LPS and then stimulated with ATP or nigericin or MSU crystal in the presence or absence of wedelolactone. The cell lysates and supernatants were collected to detect NLRP3 inflammasome components such as NLRP3, ASC and caspase 1, as well as pyroptosis and IL‐1β production. In addition, the anti‐inflammatory effects of wedelolactone on MSU‐induced peritonitis and arthritis mice were also evaluated.

          Results

          We found that wedelolactone broadly inhibited NLRP3 inflammasome activation and pyroptosis and IL‐1β secretion. Wedelolactone also block ASC oligomerization and speck formation. The inhibitory effects of wedelolactone were abrogated by PKA inhibitor H89, which also attenuated wedelolactone‐enhanced Ser/Thr phosphorylation of NLRP3 at PKA‐specific sites. Importantly, wedelolactone could abate MSU‐induced IL‐1β production and neutrophils migration into peritoneal cavity, and reduced caspase 1 (p20) and IL‐1β expression in the joint tissue of MSU‐induced arthritis.

          Conclusion

          Our results indicate that wedelolactone promotes the Ser/Thr phosphorylation of NLRP3 to inhibit inflammasome activation and pyroptosis partly through potentiating PKA signalling, thus identifying its potential use for treating MSU‐induced peritonitis and gouty arthritis.

          Abstract

          Wedelolactone is a major active ingredient of the traditional medicinal herb eclipta, which demonstrates a broad‐spectrum inhibition effect on NLRP3 inflammasome activation triggered by multiple stimuli. Wedelolactone suppresses NLRP3 inflammasome assembly, pyroptosis and IL‐1β secretion through heightening PKA‐dependent NLRP3 phosphorylation. Importantly, wedelolactone could alleviate NLRP3‐related inflammation in MSU‐induced peritonitis and gouty arthritis.

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          Most cited references34

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          The NLRP3 inflammasome: molecular activation and regulation to therapeutics

          NLRP3 (NACHT, LRR and PYD domains-containing protein 3) is an intracellular sensor that detects a broad range of microbial motifs, endogenous danger signals and environmental irritants, resulting in the formation and activation of the NLRP3 inflammasome. Assembly of the NLRP3 inflammasome leads to caspase-1-dependent release of the proinflammatory cytokines, IL-1β and IL-18, as well as to gasdermin D-mediated pyroptotic cell death. Recent studies have revealed new regulators of the NLRP3 inflammasome, including new interacting or regulatory proteins, metabolic pathways and a regulatory mitochondrial hub. In this Review, we present the molecular, cell biological and biochemical basis of NLRP3 activation and regulation, and describe how this mechanistic understanding is leading to potential therapeutics that target the NLRP3 inflammasome.
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            Dopamine controls systemic inflammation through inhibition of NLRP3 inflammasome.

            Inflammasomes are involved in diverse inflammatory diseases, so the activation of inflammasomes needs to be tightly controlled to prevent excessive inflammation. However, the endogenous regulatory mechanisms of inflammasome activation are still unclear. Here, we report that the neurotransmitter dopamine (DA) inhibits NLRP3 inflammasome activation via dopamine D1 receptor (DRD1). DRD1 signaling negatively regulates NLRP3 inflammasome via a second messenger cyclic adenosine monophosphate (cAMP), which binds to NLRP3 and promotes its ubiquitination and degradation via the E3 ubiquitin ligase MARCH7. Importantly, in vivo data show that DA and DRD1 signaling prevent NLRP3 inflammasome-dependent inflammation, including neurotoxin-induced neuroinflammation, LPS-induced systemic inflammation, and monosodium urate crystal (MSU)-induced peritoneal inflammation. Taken together, our results reveal an endogenous mechanism of inflammasome regulation and suggest DRD1 as a potential target for the treatment of NLRP3 inflammasome-driven diseases.
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              Targeting the NLRP3 inflammasome in inflammatory diseases

              This corrects the article DOI: 10.1038/nrd.2018.97.
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                Author and article information

                Contributors
                hao.pan25@foxmail.com
                chen888@gzucm.edu.cn
                Journal
                Cell Prolif
                Cell Prolif
                10.1111/(ISSN)1365-2184
                CPR
                Cell Proliferation
                John Wiley and Sons Inc. (Hoboken )
                0960-7722
                1365-2184
                12 July 2020
                September 2020
                : 53
                : 9 ( doiID: 10.1111/cpr.v53.9 )
                : e12868
                Affiliations
                [ 1 ] Research Center for Integrative Medicine School of Basic Medical Sciences Guangzhou University of Chinese Medicine Guangzhou P.R China
                [ 2 ] Dongguan & Guangzhou University of Chinese Medicine Cooperative Academy of Mathematical Engineering for Chinese Medicine Dongguan P.R China
                [ 3 ] Department of Human Anatomy School of Basic Medical Sciences Guangzhou University of Chinese Medicine Guangzhou P.R China
                [ 4 ] Center for Experimental Teaching School of Basic Medical Sciences Guangzhou University of Chinese Medicine Guangzhou P.R China
                [ 5 ] School of Chinese Herbal Medicine Guangzhou University of Chinese Medicine Guangzhou P.R China
                Author notes
                [*] [* ] Correspondence

                Hao Pan and Dongfeng Chen, No.232, East Waihuan Road, Guangzhou Higher Education Mega Centre, Panyu District, Guangzhou City, Guangdong Province, P.R China: 510006.

                Emails: hao.pan25@ 123456foxmail.com (H. P.); chen888@ 123456gzucm.edu.cn (D. C.)

                Author information
                https://orcid.org/0000-0002-2049-1842
                Article
                CPR12868
                10.1111/cpr.12868
                7507381
                32656909
                16585d51-3cec-421f-9962-f947fc1e65ea
                © 2020 The Authors. Cell Proliferation Published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 03 February 2020
                : 14 June 2020
                : 15 June 2020
                Page count
                Figures: 5, Tables: 0, Pages: 12, Words: 6897
                Funding
                Funded by: National Natural Science Foundation of China , open-funder-registry 10.13039/501100001809;
                Award ID: 81673664
                Funded by: Science and Technology Planning Project of Guangdong Province
                Award ID: 2014B090902002
                Funded by: Guangdong Basic and Applied Basic Research Foundation
                Award ID: 2019A1515110613
                Funded by: Natural Science Foundation of Guangdong Province , open-funder-registry 10.13039/501100003453;
                Award ID: 2017A030312009
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                September 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.9.1 mode:remove_FC converted:22.09.2020

                Cell biology
                gouty arthritis,nlrp3 phosphorylation,pka,pyroptosis,wedelolactone
                Cell biology
                gouty arthritis, nlrp3 phosphorylation, pka, pyroptosis, wedelolactone

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