Suppr超能文献

缺氧对健康和哮喘患者的原代人支气管平滑肌细胞的炎症和增殖反应具有双重作用。

Hypoxia exerts dualistic effects on inflammatory and proliferative responses of healthy and asthmatic primary human bronchial smooth muscle cells.

作者信息

Keglowich Laura, Baraket Melissa, Tamm Michael, Borger Peter

机构信息

Pulmonary Cell Research, Department of Biomedicine, University of Basel, Basel, Switzerland.

Sydney Medical School, The University of Sydney, Sydney, Australia.

出版信息

PLoS One. 2014 Feb 24;9(2):e89875. doi: 10.1371/journal.pone.0089875. eCollection 2014.

Abstract

BACKGROUND

For oxygen supply, airway wall cells depend on diffusion though the basement membrane, as well as on delivery by micro-vessels. In the asthmatic lung, local hypoxic conditions may occur due to increased thickness and altered composition of the basement membrane, as well as due to edema of the inflamed airway wall.

OBJECTIVE

In our study we investigated the effect of hypoxia on proliferation and pro-inflammatory and pro-angiogenic parameter production by human bronchial smooth muscle cells (BSMC). Furthermore, conditioned media of hypoxia-exposed BSMC was tested for its ability to induce sprout outgrowth from endothelial cells spheroids.

METHODS

BSMC were cultured in RPMI1640 (5% FCS) under normoxic (21% O₂) and hypoxic (1% and 5% O₂) conditions. Proliferation was determined by cell count and Western blot analysis for cyclin E and Proliferating Cell Nuclear Antigen (PCNA). Secretion of IL-6, IL-8, ENA-78 and VEGF-A was analyzed by ELISA. BSMC conditioned medium was tested for its angiogenic capacity by endothelial cell (EC)-spheroid in vitro angiogenesis assay.

RESULTS

Proliferation of BSMC obtained from asthmatic and non-asthmatic patients was significantly reduced in the presence of 1% O₂, whereas 5% O₂ reduced proliferation of asthmatic BSMC only. Hypoxia induced HIF-1α expression in asthmatic and non-asthmatic BSMC, which coincided with significantly increased release of IL-6, IL-8 and VEGF-A, but not ENA-78. Finally, endothelial sprout outgrowth from EC spheroids was increased when exposed to hypoxia conditioned BSMC medium.

CONCLUSION

Hypoxia had dualistic effects on proliferative and inflammatory responses of asthmatic and non-asthmatic BSMC. First, hypoxia reduced BSMC proliferation. Second, hypoxia induced a pro-inflammatory, pro-angiogenic response. BSMC and EC may thus be promising new targets to counteract and/or alleviate airway wall remodeling.

摘要

背景

为了获取氧气,气道壁细胞依赖于通过基底膜的扩散以及微血管的输送。在哮喘患者的肺部,由于基底膜厚度增加和成分改变,以及炎症气道壁的水肿,可能会出现局部缺氧情况。

目的

在我们的研究中,我们调查了缺氧对人支气管平滑肌细胞(BSMC)增殖以及促炎和促血管生成参数产生的影响。此外,还测试了缺氧处理的BSMC条件培养基诱导内皮细胞球体形成芽的能力。

方法

将BSMC在RPMI1640(5%胎牛血清)中于常氧(21% O₂)和缺氧(1%和5% O₂)条件下培养。通过细胞计数以及细胞周期蛋白E和增殖细胞核抗原(PCNA)的蛋白质印迹分析来测定增殖情况。通过酶联免疫吸附测定(ELISA)分析白细胞介素-6(IL-6)、白细胞介素-8(IL-8)、ENA-78和血管内皮生长因子-A(VEGF-A)的分泌。通过内皮细胞(EC)球体体外血管生成试验测试BSMC条件培养基的血管生成能力。

结果

在1% O₂存在的情况下,来自哮喘患者和非哮喘患者的BSMC增殖显著降低,而5% O₂仅降低哮喘患者BSMC的增殖。缺氧诱导哮喘患者和非哮喘患者的BSMC中缺氧诱导因子-1α(HIF-1α)表达,这与IL-6、IL-8和VEGF-A的释放显著增加一致,但ENA-78未增加。最后,当暴露于缺氧处理的BSMC培养基时,EC球体的内皮芽生长增加。

结论

缺氧对哮喘患者和非哮喘患者的BSMC增殖和炎症反应具有双重作用。首先,缺氧降低了BSMC增殖。其次,缺氧诱导了促炎、促血管生成反应。因此,BSMC和EC可能是对抗和/或减轻气道壁重塑的有前景的新靶点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验