糖尿病相关动脉粥样硬化的巨噬细胞免疫代谢。

Immunometabolism (Cobham (Surrey, England)) Pub Date : 2023-10-16 eCollection Date: 2023-10-01 DOI:10.1097/IN9.0000000000000032
Bernardo Gindri Dos Santos, Leigh Goedeke
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引用次数: 0

摘要

巨噬细胞在动脉粥样硬化斑块的形成、生长和消退中起着重要作用。这些细胞具有极强的可塑性,并根据它们受到的刺激执行不同的免疫功能。初步的体外研究已经确定了对促炎和促分解巨噬细胞的正常功能至关重要的特定代谢途径。然而,斑块微环境,特别是在胰岛素抵抗和2型糖尿病的情况下,不断通过几种同时存在的炎症和代谢刺激来挑战巨噬细胞,这可能解释了糖尿病患者动脉粥样硬化加速的原因。在这篇小型综述中,我们讨论了巨噬细胞线粒体功能和碳水化合物、脂质和氨基酸的代谢如何受到这种复杂斑块微环境的影响,以及与2型糖尿病相关的风险因素如何改变巨噬细胞的代谢重组和疾病进展。我们还简要讨论了评估巨噬细胞代谢的当前挑战,并确定了改变巨噬细胞代谢的未来工具和可能的策略,以改善糖尿病相关动脉粥样硬化的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Macrophage immunometabolism in diabetes-associated atherosclerosis.

Macrophages play fundamental roles in atherosclerotic plaque formation, growth, and regression. These cells are extremely plastic and perform different immune functions depending on the stimuli they receive. Initial in vitro studies have identified specific metabolic pathways that are crucial for the proper function of pro-inflammatory and pro-resolving macrophages. However, the plaque microenvironment, especially in the context of insulin resistance and type 2 diabetes, constantly challenges macrophages with several simultaneous inflammatory and metabolic stimuli, which may explain why atherosclerosis is accelerated in diabetic patients. In this mini review, we discuss how macrophage mitochondrial function and metabolism of carbohydrates, lipids, and amino acids may be affected by this complex plaque microenvironment and how risk factors associated with type 2 diabetes alter the metabolic rewiring of macrophages and disease progression. We also briefly discuss current challenges in assessing macrophage metabolism and identify future tools and possible strategies to alter macrophage metabolism to improve treatment options for diabetes-associated atherosclerosis.

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