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肾上腺髓质素在哮喘和 COPD 中介导促血管生成和促炎细胞因子。

Adrenomedullin mediates pro-angiogenic and pro-inflammatory cytokines in asthma and COPD.

机构信息

Clinic of Pulmonary Medicine, University Hospital Basel, Basel, Switzerland; Respiratory Cell Research, Department of Biomedicine, University of Basel, Basel, Switzerland.

Clinic of Pulmonary Medicine, University Hospital Basel, Basel, Switzerland; Respiratory Cell Research, Department of Biomedicine, University of Basel, Basel, Switzerland; Laboratory of Pharmacology, Department of Medicine, Aristotle University of Thessaloniki, Greece.

出版信息

Pulm Pharmacol Ther. 2019 Jun;56:8-14. doi: 10.1016/j.pupt.2019.01.006. Epub 2019 Jan 25.

Abstract

PURPOSE

Adrenomedullin (AM) is a pluripotent peptide hormone with contradictory effects in human health and disease. In chronic inflammatory lung diseases, such as asthma and COPD, AM has been shown to inhibit inflammation and cell proliferation. In the present study, we aimed to investigate the effect of AM on pro-angiogenic and pro-inflammatory cytokines in asthma and COPD.

PATIENTS AND METHODS

Serum levels of pro-AM were measured in patients with asthma, COPD and matched controls. The effect of AM on intracellular signaling proteins and cytokine secretion was assessed in primary cultures of epithelial cells (EC) and airway smooth muscle cells (ASMC) established from endo-bronchial biopsies of patients with asthma, COPD and controls.

RESULTS

Serum pro-AM was higher in patients with asthma and COPD, compared to controls. AM stimulated cAMP in ASMC but not in EC. In EC, AM decreased Erk1/2 MAPK expression and activation but in ASMC, AM activated Erk1/2. This effect was similar in asthma, COPD and controls. AM stimulated the secretion of pro-angiogenic CXCL1 by EC of controls and CXCL5 by EC of asthma patients. AM did not affect the secretion of IL-6 or IL-8 by EC but stimulated the secretion of IL-6 by ASMC. In EC, AM inhibited the stimulatory effect of TGF-β and IL-4 on the secretion of IL-6 and IL-8 but had an additive stimulatory effect with TGF-β in ASMC.

CONCLUSIONS

These data suggest that AM mediates the secretion of pro-angiogenic and pro-inflammatory cytokines in a cell-type and/or a disease-specific way, explaining its association with clinical outcomes in COPD.

摘要

目的

肾上腺髓质素(AM)是一种多功能肽类激素,对人类健康和疾病具有相反的作用。在慢性炎症性肺部疾病(如哮喘和 COPD)中,AM 已被证明可抑制炎症和细胞增殖。在本研究中,我们旨在研究 AM 对哮喘和 COPD 中促血管生成和促炎细胞因子的影响。

患者和方法

测量哮喘、COPD 患者和匹配对照者的血清前 AM 水平。评估 AM 对源自哮喘、COPD 和对照者的支气管活检的上皮细胞(EC)和气道平滑肌细胞(ASMC)的细胞内信号蛋白和细胞因子分泌的影响。

结果

与对照组相比,哮喘和 COPD 患者的血清前 AM 水平升高。AM 刺激 ASMC 中的 cAMP,但不刺激 EC。在 EC 中,AM 降低了 Erk1/2 MAPK 的表达和激活,但在 ASMC 中,AM 激活了 Erk1/2。这种效应在哮喘、COPD 和对照组中相似。AM 刺激对照组 EC 分泌促血管生成的 CXCL1 和哮喘患者 EC 分泌 CXCL5。AM 不影响 EC 分泌 IL-6 或 IL-8,但刺激 ASMC 分泌 IL-6。在 EC 中,AM 抑制 TGF-β和 IL-4 对 IL-6 和 IL-8 分泌的刺激作用,但在 ASMC 中与 TGF-β具有附加的刺激作用。

结论

这些数据表明,AM 通过细胞类型和/或疾病特异性方式调节促血管生成和促炎细胞因子的分泌,解释了其与 COPD 临床结局的关联。

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