IL-13 neutralization attenuates carotid artery intimal hyperplasia and increases endothelial cell migration via modulating the JAK-1/STAT-3 signaling pathway.

IL-13 neutralization attenuates carotid artery intimal hyperplasia and increases endothelial cell migration via modulating the JAK-1/STAT-3 signaling pathway.
复制标题

DOI:
10.1080/19336918.2023.2265158
复制
发表时间:
2023-12
影响因子:
3.2
通讯作者:
Chen, Chang
Chen, Chang
中科院分区:
生物学3区
文献类型:
--
作者:
Li, Qi;Li, Yue;Wu, Fengjiao;Li, Jingyu;Li, Zhongsha;Qin, Xiaoling;Wei, Simeng;Chen, Chang

文献摘要

参考文献

相似文献

本研究旨在探讨白介素13(IL-13)浓度对损伤后内皮细胞迁移调控的影响。重组人白介素13(rhIL-13)通过JAK-1/STAT-3/NOX-4信号通路显著增加HUVECs中的ROS含量。拮抗rh IL-13诱导的细胞内高ROS可促进HUVEC迁移。此外,IL-13中和不仅能抑制损伤后内膜的增殖,还能促进内皮细胞的迁移。结果提示,抑制IL-13是促进损伤后内皮细胞恢复的一种潜在手段。因此,IL-13活性的减弱可能对血管疾病有治疗价值。
The aim of this study was to investigate how the concentration of interleukin-13 (IL-13) affects the regulation of endothelial cell migration after injury. The incubation of recombinant human interleukin-13 (rhIL-13) strongly increased the content of reactive oxygen species (ROS) in HUVECs via the JAK-1/STAT-3/NOX-4 signaling pathway. Antagonizing the high intracellular ROS that was induced by rhIL-13 promoted the migration of HUVECs. Furthermore, IL-13 neutralization not only inhibited intimal hyperplasia, but also promoted the migration of endothelial cells (ECs) after injury. The results suggest that IL-13 inhibition is a potential means of stimulating endothelial cells recovery after injury. Therefore, the attenuation of IL-13 activation may have therapeutic value for vascular disease.
DOI: 10.3389/fimmu.2018.00888
发表时间: 2018
影响因子: 7.3
作者:
Junttila IS
通讯作者: Junttila IS
阿格列汀通过动脉壁内皮细胞特异性调节 SOD-1/RhoA/JNK 信号传导抑制球囊损伤后新生内膜增生
DOI: 10.1016/j.freeradbiomed.2018.04.580
发表时间: 2018-06-01
影响因子: 7.4
作者:
Li, Qi;Zhang, Mingyu;Chen, Chang
通讯作者: Chen, Chang
DOI: 10.1016/j.intimp.2017.11.032
发表时间: 2018-01-01
影响因子: 5.6
作者:
Febvre-James, Marie;Lecureur, Valerie;Fardel, Olivier
通讯作者: Fardel, Olivier
DOI: 10.1038/nm1332
发表时间: 2006-01-01
期刊: NATURE MEDICINE
影响因子: 82.9
作者:
Fichtner-Feigl, S;Strober, W;Kitani, A
通讯作者: Kitani, A
DOI: 10.1093/eurheartj/ehv564
发表时间: 2016-06-07
影响因子: 39.3
作者:
Langbein H;Brunssen C;Hofmann A;Cimalla P;Brux M;Bornstein SR;Deussen A;Koch E;Morawietz H
通讯作者: Morawietz H