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缺氧对肺泡上皮的影响。

Effects of hypoxia on the alveolar epithelium.

作者信息

Jain Manu, Sznajder Jacob Iasha

机构信息

Pulmonary Critical Care Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.

出版信息

Proc Am Thorac Soc. 2005;2(3):202-5. doi: 10.1513/pats.200501-006AC.

Abstract

An important role of the alveolar epithelium is to contribute to the alveolocapillary barrier, secrete surfactant to lower the surface tension, and clear edema. These are energy-requiring processes for which normal oxygenation is required. There are many clinical conditions in which alveolar epithelial cells are exposed to low oxygen concentrations and although they can adapt to hypoxia, there are alterations in cellular function that can impact clinical outcomes. Hypoxic alveolar cells maintain cellular ATP content by increasing glycolytic capacity and via the hypoxia inducible factor-1 activation of a myriad of genes including the vascular endothelial growth factor. In addition, they decrease ATP utilization by down regulating the high energy consuming Na,K-ATPase activity and protein synthesis. The alveolar epithelium is in close apposition to vascular endothelium, which facilitates efficient gas exchange and provides a physical barrier between luminal and interstitial/vascular spaces. Alveolar edema clearance is an active process requiring activity of many proteins of which the amiloride-sensitive sodium channel (ENaC) and Na,K-ATPase are important contributors. Exposure to hypoxia impairs alveolar edema clearance by mechanisms that down regulate both ENaC and the Na,K-ATPase function. Other effects of hypoxia on alveolar cell function include surfactant production, disruption of cytoskeleton integrity, and the triggering of apoptosis. In summary, hypoxia has deleterious effects on the alveolar epithelium. More research needs to be done to better understand the effects of hypoxia on alveolar epithelia cell and lung function.

摘要

肺泡上皮的一个重要作用是构成肺泡毛细血管屏障、分泌表面活性物质以降低表面张力以及清除水肿。这些都是需要能量的过程,而正常的氧合作用是必需的。在许多临床情况下,肺泡上皮细胞会暴露于低氧浓度环境中,尽管它们能够适应缺氧,但细胞功能会发生改变,进而可能影响临床结局。缺氧的肺泡细胞通过增加糖酵解能力以及经由缺氧诱导因子-1激活包括血管内皮生长因子在内的众多基因来维持细胞内三磷酸腺苷(ATP)含量。此外,它们通过下调高耗能的钠钾ATP酶活性和蛋白质合成来减少ATP的利用。肺泡上皮与血管内皮紧密相邻,这有利于高效的气体交换,并在管腔与间质/血管间隙之间形成物理屏障。肺泡水肿清除是一个活跃的过程,需要多种蛋白质的参与,其中氨氯地平敏感的钠通道(ENaC)和钠钾ATP酶是重要的参与者。暴露于缺氧环境会通过下调ENaC和钠钾ATP酶功能的机制损害肺泡水肿清除。缺氧对肺泡细胞功能的其他影响包括表面活性物质的产生、细胞骨架完整性的破坏以及细胞凋亡的触发。总之,缺氧对肺泡上皮有有害影响。需要开展更多研究以更好地了解缺氧对肺泡上皮细胞和肺功能的影响。

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