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首页> 外文期刊>Trends in Endocrinology and Metabolism: TEM >Efferocytosis and Atherosclerosis: Regulation of Phagocyte Function by MicroRNAs
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Efferocytosis and Atherosclerosis: Regulation of Phagocyte Function by MicroRNAs

机译:癫痫细胞症和动脉粥样硬化:MicroRNA的吞噬功能调节

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摘要

There is evidence of the critical role of efferocytosis, the clearance of apoptotic cells (ACs) by phagocytes, in vascular cell homeostasis and protection against atherosclerosis. Specific microRNAs (miRs) can regulate atherogenesis by controlling the accumulation of professional phagocytes (e.g., macrophages) and nonprofessional phagocytes (i.e., neighboring tissue cells with the ability to acquire a macrophage-like phenotype) within the arterial wall, the differentiation of phagocytes into foam cells, the efferocytosis of apoptotic foam cells by phagocytes, and the phagocyte-mediated inflammatory response. A better understanding of the mechanisms involved in miR-regulated phagocyte function might lead to novel therapeutic antiatherosclerotic strategies. In this review, we try to shed light on the relationship between miRs and cellular players in the process of efferocytosis in the context of atherosclerotic plaque and their potential as molecular targets for novel antiatherosclerotic therapies.
机译:有证据表明癫痫细胞增多,吞噬细胞(ACS)的清除在吞噬细胞,血管细胞稳态和防止动脉粥样硬化保护。特定的microRNAs(miR)可以通过控制专业吞噬细胞(例如巨噬细胞)和非营养性吞噬细胞的积累来调节α-血细胞(即,邻近组织细胞具有在动脉壁内获得巨噬细胞样表型的能力,吞噬细胞分化为泡沫细胞,通过吞噬细胞的凋亡泡沫细胞的效力细胞增多,以及吞噬细胞介导的炎症反应。更好地理解涉及miR调节的吞噬细胞功能的机制可能导致新的治疗性抗炎症策略。在这篇综述中,我们尝试在动脉粥样硬化斑块的背景下阐明MIR和蜂窝球员之间的关系,并在动脉粥样硬化的斑块的背景下的潜力,作为新的抗炎球菌粥样硬化疗法的分子靶标。

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