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Stress-induced mast cell activation contributes to atherosclerotic plaque destabilization

机译:应激诱导的肥大细胞活化导致动脉粥样硬化斑块不稳定

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Mast cells accumulate in the perivascular tissue during atherosclerotic plaque progression and contribute to plaque destabilization. However, the specific triggers for mast cell activation in atherosclerosis remain unresolved. We hypothesized that psychological stress-induced activation of mast cells may contribute to plaque destabilization. To investigate this, apoE?/? mice on Western-type diet were exposed to 120′ restraint stress. A single episode of restraint caused a significant increase in mast cell activation in the heart. In addition to a rise in serum corticosterone and changes in circulating leukocyte populations, we observed an increase in the circulating pro-inflammatory cytokine interleukin (IL)-6 in the stressed mice. Subsequent characterization of the atherosclerotic plaques revealed a high incidence and larger size of intraplaque hemorrhages in stressed mice. In mast cell-deficient apoE?/? mice, restraint stress affected circulating leukocyte levels, but did not increase plasma IL-6 levels. Furthermore, we did not observe any intraplaque hemorrhages in these mice upon stress, strongly indicating the involvement of a mast cell-dependent response to stress in atherosclerotic plaque destabilization. In conclusion, we demonstrate that acute stress activates mast cells, which induces the incidence of intraplaque hemorrhage in vivo, identifying acute stress as a risk factor for atherosclerotic plaque destabilization.
机译:肥大细胞在动脉粥样硬化斑块进展期间积聚在血管周组织中,并导致斑块不稳定。然而,动脉粥样硬化中肥大细胞激活的特定触发因素仍未解决。我们假设心理压力诱导的肥大细胞激活可能有助于斑块不稳定。要对此进行调查,apoE?/?接受西式饮食的小鼠暴露于120'的约束压力下。一次约束会导致心脏肥大细胞激活显着增加。除了血清皮质酮的升高和循环白细胞数量的变化外,我们还观察到了应激小鼠中循环促炎性细胞因子白介素(IL)-6的增加。动脉粥样硬化斑块的后续特征显示,应激小鼠中斑块内出血的发生率较高且较大。肥大细胞缺乏apoE?/?对小鼠而言,束缚应激会影响循环白细胞水平,但不会增加血浆IL-6水平。此外,我们没有观察到这些小鼠在应激后有任何斑块内出血,强烈表明动脉粥样硬化斑块失稳与肥大细胞依赖应激的反应有关。总之,我们证明了急性应激会激活肥大细胞,从而诱导体内斑块出血的发生,从而将急性应激识别为动脉粥样硬化斑块不稳定的危险因素。

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