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靶向衰老相关炎症中的细胞凋亡噬作用。

Targeting Efferocytosis in Inflammaging.

机构信息

Department of Biochemistry and Chemistry, La Trobe Institute for Molecular Science, and Research Centre for Extracellular Vesicles, La Trobe University, Melbourne, Victoria, Australia; email:

Division of Immunobiology, Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, USA; email:

出版信息

Annu Rev Pharmacol Toxicol. 2024 Jan 23;64:339-357. doi: 10.1146/annurev-pharmtox-032723-110507. Epub 2023 Aug 16.

Abstract

Rapid removal of apoptotic cells by phagocytes, a process known as efferocytosis, is key for the maintenance of tissue homeostasis, the resolution of inflammation, and tissue repair. However, impaired efferocytosis can result in the accumulation of apoptotic cells, subsequently triggering sterile inflammation through the release of endogenous factors such as DNA and nuclear proteins from membrane permeabilized dying cells. Here, we review the molecular basis of the three key phases of efferocytosis, that is, the detection, uptake, and degradation of apoptotic materials by phagocytes. We also discuss how defects in efferocytosis due to the alteration of phagocytes and dying cells can contribute to the low-grade chronic inflammation that occurs during aging, described as inflammaging. Lastly, we explore opportunities in targeting and harnessing the efferocytic machinery to limit aging-associated inflammatory diseases.

摘要

吞噬细胞快速清除凋亡细胞(即噬胞作用)是维持组织内稳态、炎症消退和组织修复的关键。然而,噬胞作用受损会导致凋亡细胞的积累,随后通过膜通透性改变的死亡细胞释放内源性因子(如 DNA 和核蛋白)引发无菌性炎症。在这里,我们综述了噬胞作用的三个关键阶段,即吞噬细胞检测、摄取和降解凋亡物质的分子基础。我们还讨论了由于吞噬细胞和死亡细胞的改变导致噬胞作用缺陷如何导致衰老过程中发生的低度慢性炎症,即炎症衰老。最后,我们探讨了靶向和利用噬胞作用机制来限制与衰老相关的炎症性疾病的机会。

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