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本文引用的文献

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Disrupting functional interactions between platelet chemokines inhibits atherosclerosis in hyperlipidemic mice.破坏血小板趋化因子之间的功能相互作用可抑制高脂血症小鼠的动脉粥样硬化。
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Different functions of monocyte subsets in familial hypercholesterolemia: potential function of CD14+ CD16+ monocytes in detoxification of oxidized LDL.家族性高胆固醇血症中单核细胞亚群的不同功能:CD14+CD16+单核细胞在氧化型低密度脂蛋白解毒中的潜在功能。
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Blood monocyte subsets differentially give rise to CD103+ and CD103- pulmonary dendritic cell populations.血液单核细胞亚群以不同方式产生CD103 +和CD103 -肺树突状细胞群体。
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单核细胞在动脉粥样硬化中的命运。

The fate of monocytes in atherosclerosis.

作者信息

Randolph G J

机构信息

Department of Gene and Cell Medicine, and the Immunology Institute, Mount Sinai School of Medicine, New York, NY 10029, USA.

出版信息

J Thromb Haemost. 2009 Jul;7 Suppl 1(Suppl 1):28-30. doi: 10.1111/j.1538-7836.2009.03423.x.

DOI:10.1111/j.1538-7836.2009.03423.x
PMID:19630762
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2862012/
Abstract

Monocytes are the primary inflammatory cell type that infiltrates early atherosclerotic plaques. Their recruitment into plaques drives disease progression. Disease interventions that target monocytes could act at several points: alteration in the phenotype of circulating monocyte subpopulations; reduced recruitment of monocytes into plaques; alterations in the survival of monocyte-derived cells in atherosclerosis; and promotion of migratory egress from plaques to bring about resolution of the plaque inflammatory response. All of these points of intervention will be briefly discussed in this article.

摘要

单核细胞是浸润早期动脉粥样硬化斑块的主要炎症细胞类型。它们募集到斑块中会推动疾病进展。针对单核细胞的疾病干预可在多个环节发挥作用:循环单核细胞亚群表型的改变;单核细胞向斑块募集的减少;动脉粥样硬化中单核细胞衍生细胞存活情况的改变;以及促进从斑块中迁移流出以促使斑块炎症反应消退。本文将简要讨论所有这些干预环节。