Rachana R, Banerjee R
School of Biosciences and Bioengineering, Indian Institute of Technology, Mumbai 400076, India.
Colloids Surf B Biointerfaces. 2006 Jun 1;50(1):9-17. doi: 10.1016/j.colsurfb.2006.03.017. Epub 2006 Mar 29.
Dipalmitoyl phosphatidylcholine (DPPC), one of the main constituents of lung surfactant is mainly responsible for reduction of surface tension to near 0 mN/m during expiration, resisting alveolar collapse. Other unsaturated phospholipids like palmitoyloleoyl phosphatidylglycerol (PG), palmitoyloleoyl phosphatidylcholine (POPC) and neutral lipids help in adsorption of lung surfactant to the air-aqueous interface. Lung surfactant lipids may interact with plasma proteins and hematological agents flooding the alveoli in diseased states. In this study, we evaluated the effects of albumin and erythrocyte membranes on spread films of DPPC alone and mixtures of DPPC with each of PG, POPC, palmitoyloleoyl phosphatidylethanolamine (PE), cholesterol (CHOL) and palmitic acid (PA) in 9:1 molar ratios. Surface tension-area isotherms were recorded using a Langmuir-Blodgett (LB) trough at 37 degrees C with 0.9% saline as the sub-phase. In the presence of erythrocyte membranes, DPPC and DPPC+PA monolayers reached minimum surface tensions of 7.3+/-0.9 and 9.6+/-1.4 mN/m, respectively. Other lipid combinations reached significantly higher minimum surface tensions >18 mN/m in presence of membranes (Newman Keul's test, p<0.05). The relative susceptibility to membrane inhibition was [(DPPC+PG, 7:3)=(DPPC+PG, 9:1)=(DPPC+POPC)=(DPPC+PE)=(DPPC+CHOL)]>[(DPPC+PA)=(DPPC)]. The differential response was more pronounced in case of albumin with DPPC and DPPC+PA monolayers reaching minimum surface tensions less than 2.4 mN/m in presence of albumin, whereas DPPC+PG and DPPC+POPC reached minimum surface tensions of around 20 mN/m in presence of albumin. Descending order of susceptibility of the spread monolayers of lipid mixtures to albumin destabilization was as follows: [(DPPC+PG, 7:3)=(DPPC+PG, 9:1)=(DPPC+POPC)]>[(DPPC+PE)=(DPPC+CHOL)]>[(DPPC+PA)=(DPPC)] The increase in minimum surface tension in presence of albumin and erythrocyte membranes was accompanied by sudden increases in compressibility at surface tensions of 15-30 mN/m. This suggests a monolayer destabilization and could be indicative of phase transitions in the mixed lipid films due to the presence of the hydrophobic constituents of erythrocyte membranes.
二棕榈酰磷脂酰胆碱(DPPC)是肺表面活性剂的主要成分之一,主要负责在呼气过程中将表面张力降低至接近0 mN/m,防止肺泡塌陷。其他不饱和磷脂,如棕榈酰油酰磷脂酰甘油(PG)、棕榈酰油酰磷脂酰胆碱(POPC)和中性脂质,有助于肺表面活性剂吸附到气-水界面。在患病状态下,肺表面活性剂脂质可能与充斥肺泡的血浆蛋白和血液学介质相互作用。在本研究中,我们评估了白蛋白和红细胞膜对单独的DPPC以及DPPC与PG、POPC、棕榈酰油酰磷脂酰乙醇胺(PE)、胆固醇(CHOL)和棕榈酸(PA)以9:1摩尔比混合的铺展膜的影响。使用Langmuir-Blodgett(LB)槽在37℃下以0.9%盐水作为亚相记录表面张力-面积等温线。在存在红细胞膜的情况下,DPPC和DPPC+PA单层分别达到最低表面张力7.3±0.9和9.6±1.4 mN/m。在存在膜的情况下,其他脂质组合达到显著更高的最低表面张力>18 mN/m(Newman Keul检验,p<0.05)。对膜抑制的相对敏感性为[(DPPC+PG, 7:3)=(DPPC+PG, 9:1)=(DPPC+POPC)=(DPPC+PE)=(DPPC+CHOL)]>[(DPPC+PA)=(DPPC)]。在白蛋白存在的情况下,差异反应更为明显,DPPC和DPPC+PA单层达到最低表面张力小于2.4 mN/m,而DPPC+PG和DPPC+POPC在白蛋白存在的情况下达到最低表面张力约20 mN/m。脂质混合物铺展单层对白蛋白去稳定作用的敏感性降序如下:[(DPPC+PG, 7:3)=(DPPC+PG, 9:1)=(DPPC+POPC)]>[(DPPC+PE)=(DPPC+CHOL)]>[(DPPC+PA)=(DPPC)] 在白蛋白和红细胞膜存在的情况下,最低表面张力的增加伴随着在15 - 30 mN/m表面张力下压缩性的突然增加。这表明单层去稳定,可能表明由于红细胞膜疏水成分的存在,混合脂质膜中发生了相变。