Notter R H, Shapiro D L, Ohning B, Whitsett J A
Chem Phys Lipids. 1987 Jun;44(1):1-17. doi: 10.1016/0009-3084(87)90002-8.
This research studies the biophysical surface activity of synthetic phospholipids combined in vitro with purified lung surfactant apoprotein, having an Mr of 6000. Hydrophobic surfactant-associated protein (SAP-6) was delipidated and purified from both bovine and canine lung lavage, and was combined in vitro with a synthetic phospholipid mixture (SM) of similar composition to natural lung surfactant phospholipids. SM phospholipids were also combined and studied biophysically with another purified surfactant-associated protein, SAP-35. The biophysical activity of synthetic phospholipid-apoprotein combinants was assessed by measurements of adsorption facility and dynamic surface tension lowering ability at 37 degrees C. The SM-SAP-6 combinants had adsorption facility equivalent to natural lung surfactant, and to the surfactant extract preparations CLSE and surfactant-TA used in exogenous surfactant replacement therapy for the neonatal Respiratory Distress Syndrome (RDS). The synthetic phospholipid-SAP-6 combinants also lowered surface tension to less than 1 dyne/cm under dynamic compression in an oscillating bubble apparatus at concentrations as low as 0.5 mg phospholipid/ml. A striking finding was that this excellent dynamic surface activity was preserved as SAP-6 composition was reduced to values as low as 5 micrograms/5 mg SM phospholipid (0.1% SAP-6 protein), an order of magnitude less than the 1% protein content of CLSE and surfactant-TA. Mixtures of SM phospholipids plus SAP-35, the major surfactant glycoprotein, had significantly lower biophysical activity, which did not approach that of a functional lung surfactant. These results suggest that synthetic exogenous surfactants of potential utility for replacement therapy in RDS can be formulated by combining synthetic phospholipids in vitro with specifically purified, hydrophobic surfactant-associated protein, SAP-6.
本研究探讨了体外合成磷脂与纯化的分子量为6000的肺表面活性蛋白结合后的生物物理表面活性。从牛和犬的肺灌洗物中脱脂并纯化了疏水表面活性蛋白(SAP - 6),并将其在体外与组成与天然肺表面活性磷脂相似的合成磷脂混合物(SM)相结合。SM磷脂还与另一种纯化的表面活性蛋白SAP - 35相结合并进行生物物理研究。通过在37℃下测量吸附能力和动态表面张力降低能力来评估合成磷脂 - 载脂蛋白组合体的生物物理活性。SM - SAP - 6组合体的吸附能力与天然肺表面活性物质以及用于新生儿呼吸窘迫综合征(RDS)外源性表面活性物质替代疗法的表面活性物质提取物制剂CLSE和表面活性物质 - TA相当。在振荡气泡装置中,合成磷脂 - SAP - 6组合体在动态压缩下,浓度低至0.5mg磷脂/ml时也能将表面张力降低至小于1达因/厘米。一个显著的发现是,当SAP - 6的组成降低至低至5微克/5mg SM磷脂(0.1% SAP - 6蛋白)时,这种出色的动态表面活性仍得以保留,这一含量比CLSE和表面活性物质 - TA的1%蛋白含量低一个数量级。SM磷脂与主要表面活性糖蛋白SAP - 35的混合物的生物物理活性显著较低,未达到功能性肺表面活性物质的水平。这些结果表明,通过在体外将合成磷脂与经过特定纯化的疏水表面活性蛋白SAP - 6相结合,可以配制出对RDS替代疗法具有潜在效用的合成外源性表面活性物质。