Department of Physiology and Medical Physics, Medical University, 6020 Innsbruck, Austria.
J Biol Chem. 2010 Sep 3;285(36):28174-82. doi: 10.1074/jbc.M110.106518. Epub 2010 Jun 17.
Pulmonary surfactant is essential for lung function. It is assembled, stored and secreted as particulate entities (lamellar body-like particles; LBPs). LBPs disintegrate when they contact an air-liquid interface, leading to an instantaneous spreading of material and a decline in surface tension. Here, we demonstrate that the film formed by the adsorbed material spontaneously segregate into distinct ordered and disordered lipid phase regions under unprecedented near-physiological conditions and, unlike natural surfactant purified from bronchoalveolar lavages, dynamically reorganized into highly viscous multilayer domains with complex three-dimensional topographies. Multilayer domains, in coexistence with liquid phases, showed a progressive stiffening and finally solidification, probably driven by a self-driven disassembly of LBPs from a sub-surface compartment. We conclude that surface film formation from LBPs is a highly dynamic and complex process, leading to a more elaborated scenario than that observed and predicted by models using reconstituted, lavaged, or fractionated preparations.
肺表面活性剂对于肺功能至关重要。它以颗粒状实体(板层小体样颗粒;LBPs)的形式组装、储存和分泌。当 LBPs 接触气液界面时会解体,导致物质瞬间铺展和表面张力下降。在这里,我们证明了在前所未有的近生理条件下,吸附材料形成的膜会自发地分离成明显的有序和无序脂质相区域,与从支气管肺泡灌洗液中纯化的天然表面活性剂不同,它会动态地重新组织成具有复杂三维形貌的高粘性多层域。多层域与液相共存时表现出逐渐变硬,最终固化,可能是由 LBPs 从亚表面隔室的自驱动解体驱动的。我们得出结论,LBPs 形成表面膜是一个高度动态和复杂的过程,导致了比使用重组、灌洗或分馏制剂的模型所观察和预测的更复杂的情况。