The roles of cholesterol in pulmonary surfactant: insights from comparative and evolutionary studies

• Published in: Comparative Biochemistry and Physiology, Part A Part A, 2001-05, Vol.129 (1), p.75-89
• Main Authors: Orgeig, Sandra, Daniels, Christopher B
• Format: Article
• Language: English
• Subjects: Animals; Biological Evolution; Body temperature; Cholesterol - metabolism; Cholesterol - physiology; Cholesterol - secretion; Evolution; Lamellar bodies; Phospholipids; Pulmonary Alveoli - metabolism; Pulmonary Alveoli - secretion; Pulmonary Surfactants - genetics; Pulmonary Surfactants - physiology; Species Specificity; Surface tension; Torpor
• ISSN: 1095-6433; 1531-4332
• DOI: 10.1016/S1095-6433(01)00307-5

In most eutherian mammals, cholesterol (Chol) comprises approximately 8–10 wt.% or 14–20 mol.% of both alveolar and lamellar body surfactant. It is regarded as an integral component of pulmonary surfactant, yet few studies have concentrated on its function or control. Throughout the evolution of the vertebrates, the contribution of cholesterol relative to surfactant phospholipids decreases, while that of the disaturated phospholipids (DSP) increases. Chol generally appears to dominate in animals with primitive bag-like lungs that lack septation, in the saccular lung of snakes or swimbladders which are not used predominantly for respiration, and also in immature lungs. It is possible that in these systems, cholesterol represents a protosurfactant. Cholesterol is controlled separately from the phospholipid (PL) component in surfactant. For example, in heterothermic mammals such as the fat-tailed dunnart, Sminthopsis crassicaudata, and the microchiropteran bat, Chalinolobus gouldii, and also in the lizard, Ctenophorus nuchalis, the relative amount of Chol increases in cold animals. During the late stages of embryonic development in chickens and lizards, the Chol to PL and Chol to DSP ratios decrease dramatically. While in isolated lizard lungs, adrenaline and acetylcholine stimulate the secretion of surfactant PL, Chol secretion remains unaffected. This is also supported in isolated cell studies of lizards and dunnarts. The rapid changes in the Chol to PL ratio in response to various physiological stimuli suggest that these two components have different turnover rates and may be packaged and processed differently. Infusion of [ 3H]cholesterol into the rat tail vein resulted in a large increase in Chol specific activity within 30 min in the lamellar body (LB) fraction, but over a 48-h period, failed to appear in the alveolar surfactant fraction. Analysis of the limiting membrane of the lamellar bodies revealed a high (76%) concentration of LB cholesterol. The majority of lamellar body Chol is, therefore, not released into the alveolar compartment, as the limiting membrane fuses with the cell membrane upon exocytosis. It appears unlikely, therefore, that lamellar bodies are the major source of alveolar Chol. It is possible that the majority of alveolar Chol is synthesised endogenously within the lung and stored independently from surfactant phospholipids. The role of cholesterol in the limiting membrane of the lamellar body may be to enable fast and easy proces