植物化学介导的efferocysis和自噬在炎症控制中的作用。

IF 6.1 2区 生物学 Q1 CELL BIOLOGY Cell Death Discovery Pub Date : 2024-12-18 DOI:10.1038/s41420-024-02254-2
Asma Vafadar, Amir Tajbakhsh, Fatemeh Hosseinpour-Soleimani, Amir Savardshtaki, Mohammad Hashem Hashempur
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引用次数: 0

摘要

Efferocytosis,凋亡细胞的清除,是维持组织稳态和免疫调节的关键过程。有缺陷的efferocytosis与慢性炎症的发展有关,包括动脉粥样硬化、神经系统疾病和自身免疫性疾病。此外,自噬和efferocytosis之间的相互作用对炎症控制至关重要,因为自噬增强了吞噬细胞的能力。有效的efferocytosis,反过来,调节自噬途径,促进平衡的细胞环境。这种平衡的失调可能导致各种疾病的发病机制。植物化学物质是在植物中发现的生物活性化合物,由于其多种药理特性,包括抗氧化、抗炎和免疫调节作用,已成为有前景的治疗药物。本文综述了植物化学物质在促进细胞胞饮和自噬中的重要作用,并探讨了植物化学物质在预防和治疗相关疾病方面的潜力。本研究探讨了植物化学物质如何影响efferocytosis的关键方面,包括吞噬细胞活化、巨噬细胞极化和自噬诱导。植物化学物质在动脉粥样硬化和神经系统疾病中的治疗潜力被强调,强调它们增强efferocytosis和自噬以及减少炎症的能力。本文还讨论了提高植物化学物质的靶向性和生物利用度的创新方法,如纳米制剂和联合疗法。最终,这项研究激发了植物化学介导的efferocytosis增强治疗慢性炎症和自身免疫性疾病的进一步研究和临床应用。
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Phytochemical-mediated efferocytosis and autophagy in inflammation control.

Efferocytosis, the clearance of apoptotic cells, is a critical process that maintains tissue homeostasis and immune regulation. Defective efferocytosis is linked to the development of chronic inflammatory conditions, including atherosclerosis, neurological disorders, and autoimmune diseases. Moreover, the interplay between autophagy and efferocytosis is crucial for inflammation control, as autophagy enhances the ability of phagocytic cells. Efficient efferocytosis, in turn, regulates autophagic pathways, fostering a balanced cellular environment. Dysregulation of this balance can contribute to the pathogenesis of various disorders. Phytochemicals, bioactive compounds found in plants, have emerged as promising therapeutic agents owing to their diverse pharmacological properties, including antioxidant, anti-inflammatory, and immunomodulatory effects. This review aims to highlight the pivotal role of phytochemicals in enhancing efferocytosis and autophagy and explore their potential in the prevention and treatment of related disorders. This study examines how phytochemicals influence key aspects of efferocytosis, including phagocytic cell activation, macrophage polarization, and autophagy induction. The therapeutic potential of phytochemicals in atherosclerosis and neurological diseases is highlighted, emphasizing their ability to enhance efferocytosis and autophagy and reduce inflammation. This review also discusses innovative approaches, such as nanoformulations and combination therapies to improve the targeting and bioavailability of phytochemicals. Ultimately, this study inspires further research and clinical applications in phytochemical-mediated efferocytosis enhancement for managing chronic inflammatory and autoimmune conditions.

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来源期刊
Cell Death Discovery
Cell Death Discovery Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
8.30
自引率
1.40%
发文量
468
审稿时长
9 weeks
期刊介绍: Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary. Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.
期刊最新文献
Correction: CK2α-mediated phosphorylation of GRP94 facilitates the metastatic cascade in triple-negative breast cancer. Insights on the crosstalk among different cell death mechanisms. Tri-specific tribodies targeting 5T4, CD3, and immune checkpoint drive stronger functional T-cell responses than combinations of antibody therapeutics. Anaerobic metabolism promotes breast cancer survival via Histone-3 Lysine-18 lactylation mediating PPARD axis. Inhibition of lanosterol synthase linking with MAPK/JNK signaling pathway suppresses endometrial cancer.
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