Olver Richard E, Walters Dafydd V, M Wilson Stuart
Tayside Institute of Child Health, Lung Membrane Transport Group, Division of Maternal and Child Health Sciences, Ninewells Hospital and Medical School, University of Dundee, Dundee DD1 9SY, United Kingdom.
Annu Rev Physiol. 2004;66:77-101. doi: 10.1146/annurev.physiol.66.071702.145229.
The developing distal lung epithelium displays an evolving liquid transport phenotype, reflecting a changing and dynamic balance between Cl- ion secretion and Na+ ion absorption, which in turn reflects changing functional requirements. Thus in the fetus, Cl--driven liquid secretion predominates throughout gestation and generates a distending pressure to stretch the lung and stimulate growth. Increasing Na+ absorptive capacity develops toward term, anticipating the switch to an absorptive phenotype at birth and beyond. There is some empirical evidence of ligand-gated regulation of Cl- transport and of regulation via changes in the driving force for Cl- secretion. Epinephrine, O2, glucocorticoid, and thyroid hormones interact to stimulate Na+ absorption by increasing Na+ pump activity and apical Na+ conductance (GNa+) to bring about the switch from net secretion to net absorption as lung liquid is cleared from the lung at birth. Postnatally, the lung lumen contains a small Cl--based liquid secretion that generates a surface liquid layer, but the lung retains a large absorptive capacity to prevent alveolar flooding and clear edema fluid. This review explores the mechanisms underlying the functional development of the lung epithelium and draws upon evidence from classic integrative physiological studies combined with molecular physiology approaches.
发育中的远端肺上皮表现出不断演变的液体运输表型,反映了氯离子分泌和钠离子吸收之间不断变化的动态平衡,这反过来又反映了不断变化的功能需求。因此,在胎儿期,氯离子驱动的液体分泌在整个妊娠期占主导地位,并产生扩张压力以伸展肺部并刺激生长。临近足月时,钠离子吸收能力逐渐增强,预示着出生及以后会转变为吸收性表型。有一些经验证据表明存在氯离子转运的配体门控调节以及通过改变氯离子分泌驱动力进行的调节。肾上腺素、氧气、糖皮质激素和甲状腺激素相互作用,通过增加钠泵活性和顶端钠离子电导(GNa+)来刺激钠离子吸收,从而在出生时肺部液体从肺中清除时实现从净分泌到净吸收的转变。出生后,肺腔含有少量基于氯离子的液体分泌,形成表面液体层,但肺仍保留很大的吸收能力以防止肺泡积水和清除水肿液。本综述探讨了肺上皮功能发育的潜在机制,并借鉴了经典整合生理学研究以及分子生理学方法的证据。