首页> 美国卫生研究院文献>American Journal of Respiratory Cell and Molecular Biology >Adenosine A2B Receptor and Hyaluronan Modulate Pulmonary Hypertension Associated with Chronic Obstructive Pulmonary Disease
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Adenosine A2B Receptor and Hyaluronan Modulate Pulmonary Hypertension Associated with Chronic Obstructive Pulmonary Disease

机译:腺苷A2B受体和乙酰透明质酸调节与慢性阻塞性肺疾病相关的肺动脉高压。

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摘要

Chronic obstructive pulmonary disease (COPD) is the fourth leading cause of death worldwide. The development of pulmonary hypertension (PH) in patients with COPD is strongly associated with increased mortality. Chronic inflammation and changes to the lung extracellular matrix (ECM) have been implicated in the pathogenesis of COPD, yet the mechanisms that lead to PH secondary to COPD remain unknown. Our experiments using human lung tissue show increased expression levels of the adenosine A2B receptor (ADORA2B) and a heightened deposition of hyaluronan (HA; a component of the ECM) in remodeled vessels of patients with PH associated with COPD. We also demonstrate that the expression of HA synthase 2 correlates with mean pulmonary arterial pressures in patients with COPD, with and without a secondary diagnosis of PH. Using an animal model of airspace enlargement and PH, we show that the blockade of ADORA2B is able to attenuate the development of a PH phenotype that correlates with reduced levels of HA deposition in the vessels and the down-regulation of genes involved in the synthesis of HA.
机译:慢性阻塞性肺疾病(COPD)是全球第四大主要死因。 COPD患者发生肺动脉高压(PH)与死亡率增加密切相关。慢性炎症和肺细胞外基质(ECM)的改变与COPD的发病机制有关,但导致COPD继发于PH的机制仍然未知。我们使用人肺组织进行的实验显示,在患有COPD的PH患者中,血管重构后腺苷A2B受体(ADORA2B)的表达水平增加,透明质酸(HA; ECM的一种成分)沉积增加。我们还证明,在有或没有继发性PH的COPD患者中,HA合酶2的表达与平均肺动脉压相关。使用空域扩大和PH的动物模型,我们表明ADORA2B的封锁能够减弱PH表型的发展,该表型与血管中HA沉积水平降低以及参与DHA合成的基因的下调相关哈。

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