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动脉粥样硬化性心血管疾病中的血液代谢重塑

Haematometabolism rewiring in atherosclerotic cardiovascular disease.

作者信息

Yvan-Charvet Laurent, Barouillet Thibault, Borowczyk Coraline

机构信息

Institut National de la Santé et de la Recherche Médicale (Inserm) U1065, Nice, France.

Université Côte d'Azur, Centre Méditerranéen de Médecine Moléculaire (C3M), Nice, France.

出版信息

Nat Rev Cardiol. 2025 Jun;22(6):414-430. doi: 10.1038/s41569-024-01108-9. Epub 2025 Jan 2.

DOI:10.1038/s41569-024-01108-9
PMID:39743562
Abstract

Atherosclerotic cardiovascular diseases are the most frequent cause of death worldwide. The clinical complications of atherosclerosis are closely linked to the haematopoietic and immune systems, which maintain homeostatic functions and vital processes in the body. The nodes linking metabolism and inflammation are receiving increasing attention because they are inextricably linked to inflammatory manifestations of non-communicable diseases, including atherosclerosis. Although metabolism and inflammation are essential to survival and involve all tissues, we still know little about how these processes influence each other. In an effort to understand these mechanisms, in this Review we explore whether and how potent cardiovascular risk factors and metabolic modifiers of atherosclerosis influence the molecular and cellular machinery of 'haematometabolism' (metabolic-dependent haematopoietic stem cell skewing) and 'efferotabolism' (metabolic-dependent efferocyte reprogramming). These changes might ultimately propagate a quantitative and qualitative drift of the macrophage supply chain and affect the clinical manifestations of atherosclerosis. Refining our understanding of the different metabolic requirements of these processes could open the possibility of developing therapeutics targeting haematometabolism that, in conjunction with improved dietary habits, help rebalance and promote efficient haematopoiesis and efferocytosis and decrease the risk of atherosclerosis complications.

摘要

动脉粥样硬化性心血管疾病是全球最常见的死亡原因。动脉粥样硬化的临床并发症与造血系统和免疫系统密切相关,这两个系统维持着体内的稳态功能和重要生理过程。连接代谢与炎症的节点正受到越来越多的关注,因为它们与包括动脉粥样硬化在内的非传染性疾病的炎症表现有着千丝万缕的联系。尽管代谢和炎症对生存至关重要且涉及所有组织,但我们对这些过程如何相互影响仍知之甚少。为了理解这些机制,在本综述中,我们探讨动脉粥样硬化的强效心血管危险因素和代谢调节因子是否以及如何影响“血液代谢”(代谢依赖性造血干细胞偏向)和“噬菌细胞代谢”(代谢依赖性噬菌细胞重编程)的分子和细胞机制。这些变化最终可能导致巨噬细胞供应链在数量和质量上发生偏移,并影响动脉粥样硬化的临床表现。深化我们对这些过程不同代谢需求的理解,可能为开发针对血液代谢的治疗方法带来可能性,这些治疗方法与改善饮食习惯相结合,有助于重新平衡并促进有效的造血和噬菌作用,降低动脉粥样硬化并发症的风险。

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Haematometabolism rewiring in atherosclerotic cardiovascular disease.动脉粥样硬化性心血管疾病中的血液代谢重塑
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本文引用的文献

1
Macrophage TREM2 as a new player in atherosclerosis.巨噬细胞中的触发受体表达于髓样细胞2(TREM2)在动脉粥样硬化中扮演新角色。
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TREM2 protects from atherosclerosis by limiting necrotic core formation.触发受体表达于髓样细胞2(TREM2)通过限制坏死核心形成来预防动脉粥样硬化。
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Efferocytosis in atherosclerosis.动脉粥样硬化中的噬作用。
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Trem2 promotes foamy macrophage lipid uptake and survival in atherosclerosis.Trem2促进动脉粥样硬化中泡沫巨噬细胞的脂质摄取和存活。
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Dysregulated cellular metabolism in atherosclerosis: mediators and therapeutic opportunities.动脉粥样硬化中细胞代谢的失调:介质和治疗机会。
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Lipid-associated macrophages transition to an inflammatory state in human atherosclerosis increasing the risk of cerebrovascular complications.在人类动脉粥样硬化中,脂质相关巨噬细胞转变为炎症状态,增加了脑血管并发症的风险。
Nat Cardiovasc Res. 2023 Jun 26;2(7):656-672. doi: 10.1038/s44161-023-00295-x.
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Bone marrow adipocytes fuel emergency hematopoiesis after myocardial infarction.骨髓脂肪细胞为心肌梗死后的应急造血提供能量。
Nat Cardiovasc Res. 2023 Dec;2(12):1277-1290. doi: 10.1038/s44161-023-00388-7. Epub 2023 Dec 5.
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Increased iron uptake by splenic hematopoietic stem cells promotes TET2-dependent erythroid regeneration.脾造血干细胞中铁摄取的增加促进了 TET2 依赖性红细胞再生。
Nat Commun. 2024 Jan 15;15(1):538. doi: 10.1038/s41467-024-44718-0.
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A time- and single-cell-resolved model of murine bone marrow hematopoiesis.一个时间和单细胞分辨的鼠骨髓造血模型。
Cell Stem Cell. 2024 Feb 1;31(2):244-259.e10. doi: 10.1016/j.stem.2023.12.001. Epub 2024 Jan 5.