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This Article Full Text Full Text (PDF) All Versions of this Article: 286/5/L1009    most recent 00342.2003v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via ISI Web of Science (8) Citing Articles via Google Scholar Google Scholar Articles by Haller, T. Articles by Putz, G. Search for Related Content PubMed PubMed Citation Articles by Haller, T. Articles by Putz, G.

Tracing surfactant transformation from cellular release to insertion into an air-liquid interface

Departments of ¹Physiology, ²Hematology and Oncology, ³Internal Medicine, ⁵Anesthesiology and Critical Care Medicine; University of Innsbruck, A-6020 Innsbruck, Austria; and ⁴Department of Gynecology and Obstetrics, State University of New York, Buffalo, New York 14222

Submitted 25 September 2003 ; accepted in final form 29 December 2003

Pulmonary surfactant is secreted by alveolar type II cells as lipid-rich, densely packed lamellar body-like particles (LBPs). The particulate nature of released LBPs might be the result of structural and/or thermodynamic forces. Thus mechanisms must exist that promote their transformation into functional units. To further define these mechanisms, we developed methods to follow LBPs from their release by cultured cells to insertion in an air-liquid interface. When released, LBPs underwent structural transformation, but did not disperse, and typically preserved a spherical appearance for days. Nevertheless, they were able to modify surface tension and exhibited high surface activity when measured with a capillary surfactometer. When LBPs inserted in an air-liquid interface were analyzed by fluorescence imaging microscopy, they showed remarkable structural transformations. These events were instantaneous but came to a halt when the interface was already occupied by previously transformed material or when surface tension was already low. These results suggest that the driving force for LBP transformation is determined by cohesive and tensile forces acting on these particles. They further suggest that transformation of LBPs is a self-regulated interfacial process that most likely does not require structural intermediates or enzymatic activation.

alveolus; lamellar body; pulmonary; secretion; surface tension

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