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动脉粥样硬化疾病中的免疫代谢。

Immunometabolism in atherosclerotic disorders.

机构信息

Division of Immunometabolism, Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.

Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.

出版信息

Nat Cardiovasc Res. 2024 Jun;3(6):637-650. doi: 10.1038/s44161-024-00473-5. Epub 2024 May 23.

Abstract

Cardiovascular diseases (CVDs), including atherosclerosis, myocardial infarction and heart failure, are the leading causes of morbidity and mortality worldwide. Emerging evidence suggests a crucial role for immune cell dysfunction and inflammation in the progression of this complex set of diseases. Recent advances demonstrate that immune cells, tightly linked to CVD pathogenesis, are sensitive to environmental signals and respond by engaging immunometabolic networks that shape their behavior. Inflammatory cues and altered nutrient availability within atherosclerotic plaques or following ischemia synergize to elicit metabolic shifts in immune cells that influence the course of disease pathology. Understanding these metabolic adaptations and how they contribute to cellular dysfunction may reveal novel therapeutic approaches for the treatment of CVD. Here we provide a comprehensive summary of the metabolic reprogramming that occurs in immune cells and their progenitors during CVD, offering insights into the potential therapeutic interventions to mitigate disease progression.

摘要

心血管疾病(CVDs)包括动脉粥样硬化、心肌梗死和心力衰竭,是全球发病率和死亡率的主要原因。新出现的证据表明,免疫细胞功能障碍和炎症在这一组复杂疾病的进展中起着关键作用。最近的进展表明,与 CVD 发病机制密切相关的免疫细胞对环境信号敏感,并通过参与免疫代谢网络来响应,这些网络塑造了它们的行为。动脉粥样硬化斑块内或缺血后炎症线索和改变的营养供应协同作用,使免疫细胞发生代谢转变,影响疾病病理过程。了解这些代谢适应及其如何导致细胞功能障碍,可能为 CVD 的治疗提供新的治疗方法。在这里,我们全面总结了 CVD 期间免疫细胞及其祖细胞发生的代谢重编程,为减轻疾病进展的潜在治疗干预提供了见解。

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