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NFκB 和 NICD 在单核细胞-巨噬细胞分化中的分子相互作用是动脉粥样硬化干预的靶点。

Molecular interaction of NFκB and NICD in monocyte-macrophage differentiation is a target for intervention in atherosclerosis.

机构信息

Department of Zoology, Unit of Biochemistry, University of Madras, Guindy Campus, Chennai, Tamil Nadu, India.

Department of Biochemistry, University of Madras, Guindy Campus, Chennai, Tamil Nadu, India.

出版信息

J Cell Physiol. 2019 May;234(5):7040-7050. doi: 10.1002/jcp.27458. Epub 2018 Nov 27.

Abstract

The activation of two transcription factors, NFκB and NICD (notch intracellular domain), plays a crucial role in different stages of atherosclerotic disease progression, from early endothelial activation by modified lipids like oxidized low-density lipoprotein (oxyLDL) to the imminent rupture of the atherosclerotic plaque. Inflammatory mediators and the notch pathway proteins were upregulated in atherogenic diet-induced rats and the same was confirmed by the differentiation of monocyte to macrophage on exposure to oxyLDL. The inflammatory transcription factor NFκB and the notch signaling transcription factor NICD were analysed for their molecular interaction in monocyte to macrophage differentiation. Inhibition of NFκB by dexamethasone in monocyte to macrophage differentiation resulted in a concomitant downregulation of NICD, whereas inhibition of NICD by N-(N-[3, 5-difluorophenacetyl])-l-alanyl)-S-phenylglycine t-butyl ester (DAPT), a γ-secretase inhibitor, did not significantly influence the expression of NFκB, but downregulated macrophage differentiation. These findings revealed that NFκB inhibition using dexamethasone regulated NICD, which turned down macrophage differentiation. Thus, inhibition of both NFκB-NICD is a potential target for intervention in atherosclerosis.

摘要

两种转录因子 NFκB 和 NICD(Notch 细胞内结构域)的激活在动脉粥样硬化疾病进展的不同阶段中起着关键作用,从早期由氧化低密度脂蛋白(oxLDL)等修饰脂质激活内皮细胞到动脉粥样硬化斑块的即将破裂。在动脉粥样硬化饮食诱导的大鼠中,炎症介质和 Notch 途径蛋白上调,并且在单核细胞暴露于 oxLDL 时向巨噬细胞分化得到证实。分析了单核细胞向巨噬细胞分化过程中 NFκB 和 Notch 信号转导转录因子 NICD 的分子相互作用。在单核细胞向巨噬细胞分化过程中用地塞米松抑制 NFκB 会导致 NICD 的伴随下调,而用 Notch 信号通路 γ-分泌酶抑制剂 N-(N-[3,5-二氟苯乙酰基])-L-丙氨酰基-S-苯甘氨酸叔丁酯(DAPT)抑制 NICD 不会显著影响 NFκB 的表达,但会下调巨噬细胞分化。这些发现表明,使用地塞米松抑制 NFκB 调节 NICD,从而抑制巨噬细胞分化。因此,抑制 NFκB-NICD 两者是动脉粥样硬化干预的潜在靶点。

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