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首页> 外文期刊>Clinical and experimental pharmacology & physiology >Interleukin-6 enhances matrix metalloproteinase-14 expression via the RAF-mitogen-activated protein kinase kinase-extracellular signal-regulated kinase 1/2-activator protein-1 pathway.
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Interleukin-6 enhances matrix metalloproteinase-14 expression via the RAF-mitogen-activated protein kinase kinase-extracellular signal-regulated kinase 1/2-activator protein-1 pathway.

机译:白细胞介素6通过RAF-促分裂原激活的蛋白激酶激酶-细胞外信号调节激酶1 / 2-激活蛋白-1途径增强基质金属蛋白酶-14的表达。

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摘要

1. Interleukin (IL)-6 is a pivotal cytokine that regulates extracellular matrix (ECM) metabolism by increasing collagen degradation via activation of matrix metalloproteinases (MMPs), such as MMP-14. In the present study, we investigated the role of IL-6 in atherosclerotic plaque and signalling pathways in apolipoprotein E-deficient (ApoE(-/-)) mice. 2. Twenty-five male ApoE(-/-) mice were fed a high-fat diet and atherosclerotic lesions in the right common carotid artery were induced by perivascular placement of a constrictive collar. Immunohistochemical analysis detected expression of IL-6 and MMP-14 in atherosclerotic lesions of the right common carotid artery. 3. On silencing activator protein (AP)-1 expression with a specific small interfering RNA, 75% of the IL-6-induced increase in MMP-14 expression was abolished through the RAF-mitogen-activated protein kinase kinase-extracellular signal-regulated kinase 1/2-AP-1 pathway. 4. These findings suggest a novel molecular pathway for inflammation-associated ECM dysregulation, which may account for atherosclerotic plaque rupture.
机译:1.白介素(IL)-6是一种关键的细胞因子,通过激活基质金属蛋白酶(MMPs)(例如MMP-14)来增加胶原蛋白的降解,从而调节细胞外基质(ECM)的代谢。在本研究中,我们调查了载脂蛋白E缺乏症(ApoE(-/-))小鼠中IL-6在动脉粥样硬化斑块和信号通路中的作用。 2.给25只雄性ApoE(-/-)小鼠喂食高脂饮食,并通过在血管周围放置颈缩项圈诱发右颈总动脉的动脉粥样硬化病变。免疫组织化学分析检测到右颈总动脉粥样硬化病变中IL-6和MMP-14的表达。 3.在使用特定的小干扰RNA沉默激活蛋白(AP)-1的表达后,通过RAF-促分裂原激活的蛋白激酶激酶-细胞外信号消除了IL-6诱导的MMP-14表达增加的75%。调节的激酶1 / 2-AP-1途径。 4.这些发现提示与炎症相关的ECM失调的新分子途径,这可能是动脉粥样硬化斑块破裂的原因。

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