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特发性肺纤维化肺部的 ROCK 激活与氧化应激。

ROCK activation in lung of idiopathic pulmonary fibrosis with oxidative stress.

机构信息

Department of Respiratory Medicine, Maebashi Red Cross Hospital, Maebashi, Gunma, Japan.

Gunma University Faculty of Health Science, Maebashi, Gunma, Japan.

出版信息

Int J Immunopathol Pharmacol. 2014 Jan-Mar;27(1):37-44. doi: 10.1177/039463201402700106.

Abstract

The Rho-associated coiled-coil containing protein kinase, (Rho-kinase or ROCK) undergoes activation by oxidative stress. ROCK-II, which is an isoform of ROCK, is activated in a murine model of lung fibrosis. The present study evaluated the level of oxidative stress and activation of ROCK-II in patients with idiopathic pulmonary fibrosis (IPF). The ROCK-II level and the phosphorylation of myosin phosphatase subunit-1 (p-MYPT-1), a hallmark of ROCK activation, were examined by immunohistochemistry of lung tissue sections. The 8-iso prostaglandin-F2alpha (8-isoPGF2alpha) level, as a marker of oxidative stress, of exhaled breath condensate was significantly higher in IPF patients than in control patients. In IPF lungs, ROCK-II was predominantly expressed by bronchial epithelial cells, as well as at a lower level by airway smooth muscle cells, vascular smooth muscle cells, and the fibroblasts of fibroblastic foci (FF). In addition, there was moderate p-MYPT-1 expression in these cells of IPF lungs. In control lungs, ROCK-II was expressed by these cells. p-MYPT-1 was weakly expressed by the bronchial epithelial cells. In conclusion, ROCK-II was activated in various lung cells of IPF patients along with oxidative stress detected by 8-isoPGF2alpha elevation. The ROCK pathway may play a role in the development of IPF oxidative stress.

摘要

Rho 相关卷曲螺旋蛋白激酶(Rho-kinase 或 ROCK)可被氧化应激激活。ROCK-II 是 ROCK 的一种同工型,在肺纤维化的小鼠模型中被激活。本研究评估了特发性肺纤维化(IPF)患者的氧化应激水平和 ROCK-II 的激活情况。通过对肺组织切片进行免疫组织化学染色,检测 ROCK-II 水平和肌球蛋白磷酸酶亚单位-1(p-MYPT-1)的磷酸化,后者是 ROCK 激活的标志。呼出气冷凝液中的 8-异前列腺素 F2alpha(8-isoPGF2alpha)水平,作为氧化应激的标志物,在 IPF 患者中明显高于对照组患者。在 IPF 肺中,ROCK-II 主要由支气管上皮细胞表达,气道平滑肌细胞、血管平滑肌细胞和纤维母细胞灶(FF)的表达水平较低。此外,这些细胞中还存在中度的 p-MYPT-1 表达。在对照组肺中,这些细胞表达 ROCK-II。p-MYPT-1 由支气管上皮细胞弱表达。总之,在特发性肺纤维化患者的各种肺细胞中,ROCK-II 被激活,同时通过 8-isoPGF2alpha 升高检测到氧化应激。ROCK 通路可能在 IPF 氧化应激的发展中起作用。

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