The L Phase of Pulmonary Surfactant.

Langmuir

Departments of Biochemistry & Molecular Biology, Medicine, and Physiology & Pharmacology , Oregon Heath & Science University, Portland , Oregon 97239-3098 , United States.

Published: June 2018

AI Article Synopsis

  • The study investigates how various components influence the structure of pulmonary surfactant using X-ray scattering techniques on samples from calf surfactant.
  • The results indicate that the surfactant consists of two bilayers with distinct leaflets, one being ordered and the other disordered, which is crucial for its function.
  • Additionally, while cholesterol does not impact the surfactant structure, the presence of anionic phospholipids is necessary for forming the L phase, and cationic surfactant proteins may inhibit the formation of this important layer at certain humidity levels.

Article Abstract

To determine how different components affect the structure of pulmonary surfactant, we measured X-ray scattering by samples derived from calf surfactant. The surfactant phospholipids demonstrated the essential characteristics of the L phase: a unit cell with a lattice constant appropriate for two bilayers, and crystalline chains detected by wide-angle X-ray scattering (WAXS). The electron density profile, obtained from scattering by oriented films at different relative humidities (70-97%), showed that the two bilayers, arranged as mirror images, each contain two distinct leaflets with different thicknesses and profiles. The detailed structures suggest one ordered leaflet that would contain crystalline chains and one disordered monolayer likely to contain the anionic compounds, which constitute ∼10% of the surfactant phospholipids. The spacing and temperature dependence detected by WAXS fit with an ordered leaflet composed of dipalmitoyl phosphatidylcholine. Physiological levels of cholesterol had no effect on this structure. Removing the anionic phospholipids prevented formation of the L phase. The cationic surfactant proteins inhibited L structures, but at levels unlikely related to charge. Because the L phase, if arranged properly, could produce a self-assembled ordered interfacial monolayer, the structure could have important functional consequences. Physiological levels of the proteins, however, inhibit formation of the L structures at high relative humidities, making their physiological significance uncertain.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6526724PMC
http://dx.doi.org/10.1021/acs.langmuir.8b00460DOI Listing

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