白细胞介素-4抑制人平滑肌细胞增殖。

Artery Pub Date : 1994-01-01
P K Vadiveloo, H R Stanton, F W Cochran, J A Hamilton
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引用次数: 0

摘要

尽管平滑肌细胞的增殖是动脉粥样硬化发病机制中的一个关键事件,但调控这种增殖的信号尚不完全清楚。增殖很可能是由斑块中发现的细胞(如T细胞)释放的细胞因子调节的。在这项研究中,我们报道了T细胞来源的细胞因子,白细胞介素-4 (IL-4),可以抑制培养的人脐动脉平滑肌细胞的增殖。IL-4浓度为20 U/ml或更高时,抑制效果最大。此外,数据显示IL-4在细胞周期的G1期早期起作用,从而阻止细胞进入S期。IL-4抑制的机制似乎不涉及刺激前列腺素合成,因为在环加氧酶抑制剂存在的情况下进行的实验获得了类似的数据。我们提出IL-4可能作为t细胞在动脉粥样硬化病变中释放的一种保护因子,以最小化斑块的大小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interleukin-4 inhibits human smooth muscle cell proliferation.

Although proliferation of smooth muscle cells is a key event in the pathogenesis of atherosclerosis, the signals which regulate this proliferation are not fully understood. It is likely that proliferation is regulated by cytokines released by cells found in the plaque, such as T cells. In this study we report that the T cell-derived cytokine, interleukin-4 (IL-4), can inhibit proliferation of cultured human umbilical artery smooth muscle cells. Maximum inhibitory effect was achieved at IL-4 concentrations of 20 U/ml or greater. In addition, the data showed that IL-4 acted early in the G1 phase of the cell cycle, thereby preventing cells from entering S phase. The mechanism of IL-4 inhibition did not appear to involve stimulation of prostanoid synthesis since similar data were obtained when experiments were performed in the presence of a cyclooxygenase inhibitor. We propose that IL-4 may act as a protective factor released by T-cells in an atherosclerotic lesion in order to minimise the size of the plaque.

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