Kostyunina Daria S, Rowan Simon C, Pakhomov Nikolai V, Dillon Eugene, Rochfort Keith D, Cummins Philip M, O'Rourke Malachy J, McLoughlin Paul
School of Medicine.
Conway Institute of Biomolecular and Biomedical Research, and.
Am J Respir Cell Mol Biol. 2023 May;68(5):551-565. doi: 10.1165/rcmb.2022-0340OC.
Blood flow produces shear stress that homeostatically regulates the phenotype of pulmonary endothelial cells, exerting antiinflammatory and antithrombotic actions and maintaining normal barrier function. Hypoxia due to diseases, such as chronic obstructive pulmonary disease (COPD), causes vasoconstriction, increased vascular resistance, and pulmonary hypertension. Hypoxia-induced changes in endothelial function play a central role in the development of pulmonary hypertension. However, the interactive effects of hypoxia and shear stress on the pulmonary endothelial phenotype have not been studied. Human pulmonary microvascular endothelial cells were cultured in normoxia or hypoxia while subjected to physiological shear stress or in static conditions. Unbiased proteomics was used to identify hypoxia-induced changes in protein expression. Using publicly available single-cell RNA sequencing datasets, differences in gene expression between the alveolar endothelial cells from COPD and healthy lungs were identified. Sixty proteins were identified whose expression changed in response to hypoxia in conditions of physiological shear stress but not in static conditions. These included proteins that are crucial for endothelial homeostasis (e.g., JAM-A [junctional adhesion molecule A], ERG [ETS transcription factor ERG]) or implicated in pulmonary hypertension (e.g., thrombospondin-1). Fifty-five of these 60 have not been previously implicated in the development of hypoxic lung diseases. mRNA for 5 of the 60 (ERG, MCRIP1 [MAPK regulated corepressor interacting protein 1], EIF4A2 [eukaryotic translation initiation factor 4A2], HSP90AA1 [heat shock protein 90 alpha family class A member 1], and DNAJA1 [DnaJ Hsp40 (heat shock protein family) member A1]) showed similar changes in the alveolar endothelial cells of COPD compared with healthy lungs in females but not in males. These data show that the proteomic responses of the pulmonary microvascular endothelium to hypoxia are significantly altered by shear stress and suggest that these shear-hypoxia interactions are important in the development of hypoxic pulmonary vascular disease.
血流产生剪切应力,该应力通过稳态调节肺内皮细胞的表型,发挥抗炎和抗血栓形成作用,并维持正常的屏障功能。诸如慢性阻塞性肺疾病(COPD)等疾病引起的缺氧会导致血管收缩、血管阻力增加和肺动脉高压。缺氧诱导的内皮功能变化在肺动脉高压的发展中起核心作用。然而,缺氧和剪切应力对肺内皮细胞表型的相互作用尚未得到研究。人肺微血管内皮细胞在常氧或缺氧条件下培养,同时施加生理剪切应力或处于静态条件。使用非偏向蛋白质组学来鉴定缺氧诱导的蛋白质表达变化。利用公开可用的单细胞RNA测序数据集,确定了COPD患者和健康肺组织肺泡内皮细胞之间的基因表达差异。鉴定出60种蛋白质,其表达在生理剪切应力条件下对缺氧有反应,但在静态条件下无反应。这些蛋白质包括对内皮稳态至关重要的蛋白质(例如,JAM-A [连接粘附分子A]、ERG [ETS转录因子ERG])或与肺动脉高压有关的蛋白质(例如,血小板反应蛋白-1)。这60种蛋白质中有55种以前未被认为与缺氧性肺疾病的发展有关。60种蛋白质中的5种(ERG、MCRIP1 [丝裂原活化蛋白激酶调节的共抑制因子相互作用蛋白1]、EIF4A2 [真核翻译起始因子4A2]、HSP90AA1 [热休克蛋白90α家族A类成员1]和DNAJA1 [DnaJ热休克蛋白40(热休克蛋白家族)成员A1])的mRNA在女性COPD患者的肺泡内皮细胞中与健康肺组织相比显示出相似的变化,但在男性中未显示。这些数据表明,剪切应力显著改变了肺微血管内皮对缺氧的蛋白质组学反应,并表明这些剪切-缺氧相互作用在缺氧性肺血管疾病的发展中很重要。