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真菌毒素具有诱导细胞衰老的潜力:对真菌毒素免疫毒性的新认识。

Mycotoxins have a potential of inducing cell senescence: A new understanding of mycotoxin immunotoxicity.

机构信息

College of Life Science, Yangtze University, Jingzhou 434025, China.

Department of Chemistry, Faculty of Science, University of Hradec Králové, Hradec Králové 50003, Czech Republic.

出版信息

Environ Toxicol Pharmacol. 2023 Aug;101:104188. doi: 10.1016/j.etap.2023.104188. Epub 2023 Jun 17.

Abstract

Mycotoxins result in immune dysfunction and cause immune diseases in animals and humans. However, the mechanisms of immunotoxicity involved in mycotoxins have not been fully explored, and emerging evidence suggests that these toxins may promote their immunotoxicity via cellular senescence. Mycotoxins induce cell senescence after DNA damage, and activate signaling via the NF-κB and JNK pathways to promote the secretion of senescence-associated secretory phenotype (SASP) cytokines including IL-6, IL-8, and TNF-α. DNA damage can also over-activate or cleave poly (ADP-ribose) polymerase-1 (PARP-1), increase the expression of cell cycle inhibitory proteins p21, and p53, and induce cell cycle arrest and then senescence. These senescent cells further down-regulate proliferation-related genes and overexpress inflammatory factors resulting in chronic inflammation and eventual immune exhaustion. Here we review the underlying mechanisms by which mycotoxins trigger cell senescence and the potential roles of SASP and PARP in these pathways. This work will help to further understand the mechanisms of immunotoxicity involved in mycotoxins.

摘要

真菌毒素会导致免疫功能障碍,并在动物和人类中引发免疫性疾病。然而,真菌毒素所涉及的免疫毒性机制尚未被充分探索,新出现的证据表明,这些毒素可能通过细胞衰老来促进其免疫毒性。真菌毒素在 DNA 损伤后诱导细胞衰老,并通过 NF-κB 和 JNK 信号通路激活来促进衰老相关分泌表型 (SASP) 细胞因子的分泌,包括 IL-6、IL-8 和 TNF-α。DNA 损伤还可以过度激活或切割聚 (ADP-核糖) 聚合酶-1 (PARP-1),增加细胞周期抑制蛋白 p21 和 p53 的表达,诱导细胞周期停滞和衰老。这些衰老细胞进一步下调与增殖相关的基因,并过度表达炎症因子,导致慢性炎症和最终的免疫衰竭。在这里,我们综述了真菌毒素引发细胞衰老的潜在机制,以及 SASP 和 PARP 在这些途径中的潜在作用。这项工作将有助于进一步了解真菌毒素所涉及的免疫毒性机制。

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