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      Crosstalk between cholesterol metabolism and psoriatic inflammation

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          Abstract

          Psoriasis is a chronic autoinflammatory skin disease associated with multiple comorbidities, with a prevalence ranging from 2 to 3% in the general population. Decades of preclinical and clinical studies have revealed that alterations in cholesterol and lipid metabolism are strongly associated with psoriasis. Cytokines (tumor necrosis factor-α (TNF-α), interleukin (IL)-17), which are important in the pathogenesis of psoriasis, have been shown to affect cholesterol and lipid metabolism. Cholesterol metabolites and metabolic enzymes, on the other hand, influence not only the biofunction of keratinocytes (a primary type of cell in the epidermis) in psoriasis, but also the immune response and inflammation. However, the relationship between cholesterol metabolism and psoriasis has not been thoroughly reviewed. This review mainly focuses on cholesterol metabolism disturbances in psoriasis and their crosstalk with psoriatic inflammation.

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          Most cited references185

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          Pathophysiology, Clinical Presentation, and Treatment of Psoriasis: A Review

          Approximately 125 million people worldwide have psoriasis. Patients with psoriasis experience substantial morbidity and increased rates of inflammatory arthritis, cardiometabolic diseases, and mental health disorders.
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            Mechanisms and regulation of cholesterol homeostasis

            Cholesterol homeostasis is vital for proper cellular and systemic functions. Disturbed cholesterol balance underlies not only cardiovascular disease but also an increasing number of other diseases such as neurodegenerative diseases and cancers. The cellular cholesterol level reflects the dynamic balance between biosynthesis, uptake, export and esterification - a process in which cholesterol is converted to neutral cholesteryl esters either for storage in lipid droplets or for secretion as constituents of lipoproteins. In this Review, we discuss the latest advances regarding how each of the four parts of cholesterol metabolism is executed and regulated. The key factors governing these pathways and the major mechanisms by which they respond to varying sterol levels are described. Finally, we discuss how these pathways function in a concerted manner to maintain cholesterol homeostasis.
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              Pleiotropic roles of bile acids in metabolism.

              Enzymatic oxidation of cholesterol generates numerous distinct bile acids that function both as detergents that facilitate digestion and absorption of dietary lipids, and as hormones that activate four distinct receptors. Activation of these receptors alters gene expression in multiple tissues, leading to changes not only in bile acid metabolism but also in glucose homeostasis, lipid and lipoprotein metabolism, energy expenditure, intestinal motility and bacterial growth, inflammation, liver regeneration, and hepatocarcinogenesis. This review covers the roles of specific bile acids, synthetic agonists, and their cognate receptors in controlling these diverse functions, as well as their current use in treating human diseases. Copyright © 2013 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                10 May 2023
                2023
                : 14
                : 1124786
                Affiliations
                [1] 1 Department of Dermatology, Hospital for Skin Disease, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College , Nanjing, Jiangsu, China
                [2] 2 Department of Dermatology, Jiangsu Key Laboratory of Molecular Biology for Skin Diseases and Sexually Transmitted Infections , Nanjing, Jiangsu, China
                Author notes

                Edited by: Fang Zheng, Xi’an Jiaotong University, China

                Reviewed by: Neal Lee Weintraub, Augusta University, United States; William Griffiths, Swansea University, United Kingdom

                *Correspondence: Chengrang Li, dr_lcr72@ 123456163.com
                Article
                10.3389/fimmu.2023.1124786
                10206135
                37234169
                25cc215e-09f9-4b2c-b04c-6b79e95fcbde
                Copyright © 2023 Luo, Guo, Chen, Zhu and Li

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 15 December 2022
                : 26 April 2023
                Page count
                Figures: 3, Tables: 0, Equations: 0, References: 185, Pages: 15, Words: 7987
                Funding
                Funded by: Natural Science Foundation of Jiangsu Province , doi 10.13039/501100004608;
                Award ID: BK20211027
                This research was supportedby CAMS Innovation Fund for Medical Sciences (CIFMS) (grant number: 2021-I2M-1-001, 2021-I2M-1-018, 2021-I2M-1-059), the Special Research Fund for Central Universities, Peking Union Medical College (grant number: 3332022156) and the Natural Science Foundation of Jiangsu province (grant numbers: BK20211027).
                Categories
                Immunology
                Review
                Custom metadata
                Inflammation

                Immunology
                cholesterol metabolism,immunity,inflammation,immunometabolism,psoriatic inflammation
                Immunology
                cholesterol metabolism, immunity, inflammation, immunometabolism, psoriatic inflammation

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