Putz G, Walch M, Van Eijk M, Haagsman H P
Department of Anesthesia and Intensive Care Medicine, Leopold-Franzens-University of Innsbruck, Austria.
Biochim Biophys Acta. 1999 Jan 6;1453(1):126-34. doi: 10.1016/s0925-4439(98)00092-1.
The biophysical activity of lung surfactant depends, to a large extent, on the presence of the hydrophobic surfactant proteins B (SP-B) and C (SP-C). The role of these proteins in lipid adsorption and lipid squeeze-out under dynamic conditions simulating breathing is not yet clear. Therefore, the aim of this study was to investigate the interaction of spread hydrophobic surfactant proteins with phospholipids in a captive-bubble surfactometer during rapid cyclic area changes (6 cycles/min). We found that SP-B and SP-C facilitated the rapid transport of lipids into the air-water interface in a concentration-dependent manner (threshold concentration > or = 0.05:0.5 mol% SP-B/SP-C). Successive rapid cyclic area changes did not affect the concentration-dependent lipid adsorption process, suggesting that SP-B and SP-C remained associated with the surface film.
肺表面活性剂的生物物理活性在很大程度上取决于疏水表面活性剂蛋白B(SP-B)和C(SP-C)的存在。在模拟呼吸的动态条件下,这些蛋白在脂质吸附和脂质挤出过程中的作用尚不清楚。因此,本研究的目的是在快速循环面积变化(6次/分钟)期间,研究在俘获气泡表面张力仪中展开的疏水表面活性剂蛋白与磷脂的相互作用。我们发现,SP-B和SP-C以浓度依赖的方式促进脂质快速转运到气-水界面(阈值浓度>或 = 0.05:0.5 mol% SP-B/SP-C)。连续的快速循环面积变化并未影响浓度依赖的脂质吸附过程,这表明SP-B和SP-C仍与表面膜结合。