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本文引用的文献

1
Ly-6Chi monocytes dominate hypercholesterolemia-associated monocytosis and give rise to macrophages in atheromata.Ly-6Chi单核细胞在高胆固醇血症相关的单核细胞增多症中占主导地位,并在动脉粥样硬化斑块中产生巨噬细胞。
J Clin Invest. 2007 Jan;117(1):195-205. doi: 10.1172/JCI29950.
2
Monocyte subsets differentially employ CCR2, CCR5, and CX3CR1 to accumulate within atherosclerotic plaques.单核细胞亚群以不同方式利用CCR2、CCR5和CX3CR1在动脉粥样硬化斑块内聚集。
J Clin Invest. 2007 Jan;117(1):185-94. doi: 10.1172/JCI28549.
3
Obesity induces a phenotypic switch in adipose tissue macrophage polarization.肥胖会导致脂肪组织巨噬细胞极化发生表型转变。
J Clin Invest. 2007 Jan;117(1):175-84. doi: 10.1172/JCI29881.
4
Inflammation and insulin resistance.炎症与胰岛素抵抗
J Clin Invest. 2006 Jul;116(7):1793-801. doi: 10.1172/JCI29069.
5
Monocyte and macrophage heterogeneity.单核细胞和巨噬细胞的异质性。
Nat Rev Immunol. 2005 Dec;5(12):953-64. doi: 10.1038/nri1733.
6
Heterogeneity of thymic dendritic cells.胸腺树突状细胞的异质性
Semin Immunol. 2005 Aug;17(4):304-12. doi: 10.1016/j.smim.2005.05.001.
7
Macrophage receptors and immune recognition.巨噬细胞受体与免疫识别。
Annu Rev Immunol. 2005;23:901-44. doi: 10.1146/annurev.immunol.23.021704.115816.
8
Blood monocytes consist of two principal subsets with distinct migratory properties.血液单核细胞由两个具有不同迁移特性的主要亚群组成。
Immunity. 2003 Jul;19(1):71-82. doi: 10.1016/s1074-7613(03)00174-2.
9
Chemokine receptor mutant CX3CR1-M280 has impaired adhesive function and correlates with protection from cardiovascular disease in humans.趋化因子受体突变体CX3CR1-M280具有受损的黏附功能,且与人类心血管疾病的防护相关。
J Clin Invest. 2003 Apr;111(8):1241-50. doi: 10.1172/JCI16790.
10
Scavenger receptors in innate immunity.天然免疫中的清道夫受体。
Curr Opin Immunol. 2002 Feb;14(1):123-8. doi: 10.1016/s0952-7915(01)00307-7.

巨噬细胞异质性与组织脂质

Macrophage heterogeneity and tissue lipids.

作者信息

Gordon Siamon

机构信息

Sir William Dunn School of Pathology, University of Oxford, Oxford, United Kingdom.

出版信息

J Clin Invest. 2007 Jan;117(1):89-93. doi: 10.1172/JCI30992.

DOI:10.1172/JCI30992
PMID:17200712
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1716225/
Abstract

Macrophages are present as resident cells in adipose tissue, and blood monocytes are recruited in increased numbers to sites of lipid accumulation in atherosclerosis, a modified form of inflammation in the arterial wall. Recent findings reported by 3 separate groups in this issue of the JCI provide evidence for distinct monocyte subsets, differential chemokine receptor usage, and phenotypic modulation of macrophages in murine models of genetic and high-fat diet-induced disease (see the related articles beginning on pages 175, 185, and 195). These studies raise prospects for selective therapeutic targets to ameliorate macrophage hyperinflammatory responses, while sparing host defense and repair mechanisms.

摘要

巨噬细胞作为驻留细胞存在于脂肪组织中,在动脉粥样硬化(一种动脉壁炎症的改良形式)的脂质积聚部位,血液中的单核细胞会大量募集。本期《临床研究杂志》上3个独立研究小组报道的最新发现,为小鼠遗传和高脂饮食诱导疾病模型中不同的单核细胞亚群、趋化因子受体的不同使用情况以及巨噬细胞的表型调节提供了证据(见第175、185和195页开始的相关文章)。这些研究为选择性治疗靶点带来了希望,以改善巨噬细胞的过度炎症反应,同时保留宿主防御和修复机制。