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组成型光形态建成9信号体亚基5与程序性细胞死亡蛋白1配体在哮喘中的作用

Involvement of the Constitutive Photomorphogenesis 9 Signalosome Subunit 5 With Programmed Cell Death Protein 1 Ligand in Asthma.

作者信息

Choi Seon-Muk, An Min-Hyeok, Lee Pureun-Haneul, Hwang DaYeon, Nam Yunha, Park Shinhee, Jang An-Soo

机构信息

Division of Allergy and Respiratory Medicine, Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, Korea.

出版信息

Allergy Asthma Immunol Res. 2024 Sep;16(5):505-519. doi: 10.4168/aair.2024.16.5.505.

Abstract

PURPOSE

The constitutive photomorphogenesis 9 signalosome (CSN) is a highly conserved protein complex comprised of eight subunits, each of which play crucial roles in diverse cellular processes, such as signal transduction, gene transcription, angiogenesis, and cell proliferation. In the context of asthma, a potential emerging target is the programmed death-ligand 1 (PD-L1)-mediated pathway, which serves as a significant immune checkpoint inhibitor in this condition. However, the precise involvement of CSN subunit 5 (CSN5) in bronchial asthma and the interplay between CSN5 and PD-L1 in asthma remain poorly understood.

METHODS

The potential association between CSN5 and bronchial asthma was explored in a mouse model of ovalbumin (OVA)-induced asthma. Samples were obtained from human lung microvascular endothelial cell (HMVEC-L) treated with () and CSN5 small interfering RNA. The expression of nuclear factor (NF)-κB, IκBα, inhibitor of κB kinase β (IKKβ), PD-L1, and CSN5 was assessed. Additionally, plasma CSN5 levels in asthma patients, both in stable and exacerbated states, were examined.

RESULTS

Plasma levels of CSN5 were elevated in patients with exacerbated asthma (n = 19) compared to both healthy controls (n = 10) and patients with stable asthma (n = 19). The CSN5 level demonstrated a correlation with lung function in individuals with asthma. Silencing CSN5 in HMVEC-L led to a reduction in NF-κB protein levels at 4 hours and PD-L1 levels at 4, 8, and 24 hours after treatment. In OVA-sensitized/challenged mice, goblet cell hyperplasia, lung fibrosis, and the levels of CSN5, PD-L1, interleukin-13, interferon-γ, phospho (p)-NF-κB, p-IκBα, and p-IKKβ proteins increased at 33 and 80 days compared to control mice. However, these changes were mitigated by treatment with a PD-L1 inhibitor.

CONCLUSIONS

These findings suggest that CSN5, along with PD-L1, could serve as a promising target for the treatment of asthma.

摘要

目的

组成型光形态建成9信号体(CSN)是一种高度保守的蛋白质复合物,由八个亚基组成,每个亚基在多种细胞过程中发挥关键作用,如信号转导、基因转录、血管生成和细胞增殖。在哮喘的背景下,一个潜在的新兴靶点是程序性死亡配体1(PD-L1)介导的途径,该途径在这种情况下作为一种重要的免疫检查点抑制剂。然而,CSN亚基5(CSN5)在支气管哮喘中的具体作用以及CSN5与PD-L1在哮喘中的相互作用仍知之甚少。

方法

在卵清蛋白(OVA)诱导的哮喘小鼠模型中探讨CSN5与支气管哮喘之间的潜在关联。从用()和CSN5小干扰RNA处理的人肺微血管内皮细胞(HMVEC-L)中获取样本。评估核因子(NF)-κB、IκBα、κB激酶β(IKKβ)抑制剂、PD-L1和CSN5的表达。此外,还检测了哮喘患者稳定期和加重期血浆中CSN5的水平。

结果

与健康对照组(n = 10)和稳定期哮喘患者(n = 19)相比,加重期哮喘患者(n = 19)的血浆CSN5水平升高。CSN5水平与哮喘患者的肺功能相关。在HMVEC-L中沉默CSN5导致处理后4小时NF-κB蛋白水平以及处理后4、8和24小时PD-L1水平降低。在OVA致敏/激发的小鼠中,与对照小鼠相比,杯状细胞增生、肺纤维化以及CSN5、PD-L1、白细胞介素-13、干扰素-γ、磷酸化(p)-NF-κB、p-IκBα和p-IKKβ蛋白水平在第33天和第80天升高。然而,用PD-L1抑制剂治疗可减轻这些变化。

结论

这些发现表明,CSN5与PD-L1一起可能是治疗哮喘的有前景的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1967/11450436/d3d8dbe3b3e0/aair-16-505-g001.jpg

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