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      The Effect of Lycium barbarum Polysaccharides on Pyroptosis-Associated Amyloid β 1-40 Oligomers-Induced Adult Retinal Pigment Epithelium 19 Cell Damage

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          Abstract

          Age-related macular degeneration (AMD) is a sight-threatening disease with limited treatment options. We investigated whether amyloid β 1-40 (Aβ 1-40) could cause pyroptosis and evaluated the effects of Lycium barbarum polysaccharides (LBP) on Aβ 1-40 oligomers-induced retinal pigment epithelium 19 (ARPE-19) damage, which is an in vitro AMD model. Aβ 1-40 oligomers verified by Western blot were added to ARPE-19 cells with or without 24 h LBP treatment. Aβ 1-40 oligomers significantly decreased ARPE-19 cell viability with obvious morphological changes under light microscopy. SEM revealed swollen cells with a bubbling appearance and ruptured cell membrane, which are morphological characteristics of pyroptosis. ELISA results showed increased expression of IL-1β and IL-18, which are the final products of pyroptosis. LBP administration for 24 h had no toxic effects on ARPE-19 cells and improved cell viability and morphology while disrupting Aβ 1-40 oligomerization in a dose-dependent manner. Furthermore, Aβ 1-40 oligomers up-regulated the cellular immunoreactivity of pyroptosis markers including NOD-like receptors protein 3 (NLRP3), caspase-1, and membrane N-terminal cleavage product of GSDMD (GSDMD-N), which could be reversed by LBP treatment. Taken together, this study showed that LBP effectively protects the Aβ 1-40 oligomers-induced pyroptotic ARPE-19 cell damages by its anti-Aβ 1-40 oligomerization properties and its anti-pyroptotic effects.

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          Most cited references33

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          Quantitative analysis of histological staining and fluorescence using ImageJ.

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            Caspases in Cell Death, Inflammation, and Pyroptosis

            Caspases are a family of conserved cysteine proteases that play key roles in programmed cell death and inflammation. In multicellular organisms, caspases are activated via macromolecular signaling complexes that bring inactive procaspases together and promote their proximity-induced autoactivation and proteolytic processing. Activation of caspases ultimately results in programmed execution of cell death, and the nature of this cell death is determined by the specific caspases involved. Pioneering new research has unraveled distinct roles and cross talk of caspases in the regulation of programmed cell death, inflammation, and innate immune responses. In-depth understanding of these mechanisms is essential to foster the development of precise therapeutic targets to treat autoinflammatory disorders, infectious diseases, and cancer. This review focuses on mechanisms governing caspase activation and programmed cell death with special emphasis on the recent progress in caspase cross talk and caspase-driven gasdermin D–induced pyroptosis.
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              The mechanisms of NLRP3 inflammasome/pyroptosis activation and their role in Parkinson's disease

              Parkinson's disease (PD) is a typical neurodegenerative disease and the pathological feature of which is the death of dopamine neurons in the substantia nigra region. At present, neuronal death caused by inflammatory cytokine-mediated neuroinflammation is being extensively studied. The nucleotide-binding oligomerization domain-, leucine-rich repeat and pyrin domain-containing 3 (NLRP3) inflammasome is an inflammatory complex existing in microglia. Its activation promotes the secretion of the inflammatory cytokine interleukin-1β/18 (IL-1β/18) and induces pyroptosis, a type of cell death that possesses the potential for inflammation, to rupture microglia to further release IL-1β. In this review we focus on the mechanisms of activation of the NLRP3 inflammasome and pyroptosis and their inflammatory effects on the development of PD. In addition, we focus on some inhibitors of NLRP3 inflammatory pathways to alleviate the progression of PD by inhibiting central inflammation and provide new therapeutic strategies for the treatment of PD.
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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                30 June 2020
                July 2020
                : 21
                : 13
                : 4658
                Affiliations
                [1 ]Department of Ophthalmology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China; hrmeym@ 123456hku.hk (M.Y.); hrmaskf@ 123456hku.hk (K.-F.S.)
                [2 ]State Key Laboratory of Brain and Cognitive Sciences, The University of Hong Kong, Hong Kong, China
                Author notes
                [* ]Correspondence: amylo@ 123456hku.hk (A.C.Y.L.); waichlam@ 123456hku.hk (W.C.L.)
                Author information
                https://orcid.org/0000-0001-8600-4325
                https://orcid.org/0000-0003-4239-6851
                Article
                ijms-21-04658
                10.3390/ijms21134658
                7369740
                32629957
                5b5fcc59-380c-4aad-b818-132343ce0f5a
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 19 May 2020
                : 28 June 2020
                Categories
                Article

                Molecular biology
                cell death,drusen,eye disease,retina,traditional chinese medicine (tcm)
                Molecular biology
                cell death, drusen, eye disease, retina, traditional chinese medicine (tcm)

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