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衰老与动脉粥样硬化:血管的内在和外在因素及 IL-6 的潜在作用。

Ageing and atherosclerosis: vascular intrinsic and extrinsic factors and potential role of IL-6.

机构信息

Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.

Department of Microbiology and Immunology, University of Michigan, Ann Arbor, MI, USA.

出版信息

Nat Rev Cardiol. 2021 Jan;18(1):58-68. doi: 10.1038/s41569-020-0431-7. Epub 2020 Sep 11.

DOI:10.1038/s41569-020-0431-7
PMID:32918047
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7484613/
Abstract

The number of old people is rising worldwide, and advancing age is a major risk factor for atherosclerotic cardiovascular disease. However, the mechanisms underlying this phenomenon remain unclear. In this Review, we discuss vascular intrinsic and extrinsic mechanisms of how ageing influences the pathology of atherosclerosis. First, we focus on factors that are extrinsic to the vasculature. We discuss how ageing affects the development of myeloid cells leading to the expansion of certain myeloid cell clones and induces changes in myeloid cell functions that promote atherosclerosis via inflammation, including a potential role for IL-6. Next, we describe vascular intrinsic factors by which ageing promotes atherogenesis - in particular, the effects on mitochondrial function. Studies in mice and humans have shown that ageing leads to a decline in vascular mitochondrial function and impaired mitophagy. In mice, ageing is associated with an elevation in the levels of the inflammatory cytokine IL-6 in the aorta, which participates in a positive feedback loop with the impaired vascular mitochondrial function to accelerate atherogenesis. We speculate that vascular and myeloid cell ageing synergize, via IL-6 signalling, to accelerate atherosclerosis. Finally, we propose future avenues of clinical investigation and potential therapeutic approaches to reduce the burden of atherosclerosis in old people.

摘要

全球老年人口数量不断增加,年龄增长是动脉粥样硬化性心血管疾病的主要危险因素。然而,这一现象的背后机制尚不清楚。在这篇综述中,我们讨论了衰老影响动脉粥样硬化病理的血管固有和外在机制。首先,我们关注血管外的因素。我们讨论了衰老如何影响髓样细胞的发育,导致某些髓样细胞克隆的扩张,并通过炎症促进动脉粥样硬化的发生,包括白细胞介素 6(IL-6)的潜在作用。接下来,我们描述了衰老促进动脉粥样硬化形成的血管固有因素,特别是对线粒体功能的影响。在小鼠和人类中的研究表明,衰老导致血管中线粒体功能下降和自噬受损。在小鼠中,衰老与主动脉中促炎细胞因子白细胞介素 6(IL-6)水平的升高有关,IL-6 与受损的血管线粒体功能一起参与正反馈循环,从而加速动脉粥样硬化的发生。我们推测,血管和髓样细胞衰老通过 IL-6 信号协同作用,加速动脉粥样硬化的发生。最后,我们提出了未来临床研究的方向和潜在的治疗方法,以减轻老年人动脉粥样硬化的负担。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5983/7484613/3c8744f61c78/41569_2020_431_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5983/7484613/dec6f2796dd4/41569_2020_431_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5983/7484613/3c8744f61c78/41569_2020_431_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5983/7484613/dec6f2796dd4/41569_2020_431_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5983/7484613/3c8744f61c78/41569_2020_431_Fig2_HTML.jpg

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