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J. Biol. Chem., Vol. 267, Issue 28, 19884-19890, Oct, 1992
A Suwabe, RJ Mason, D Smith, JA Firestone, MD Browning and DR Voelker
Pulmonary alveolar type II cells synthesize, secrete, and recycle the
components of pulmonary surfactant. In this report we present evidence that
dipalmitoylphosphatidylcholine is a potent inhibitor of surfactant lipid
secretion by type II cells. Monoenoic and dienoic phosphatidylcholines with
fatty acids of 16 or 18 carbons are ineffective as inhibitors of surfactant
lipid secretion. In contrast, disaturated phosphatidylcholines, with either
symmetric or asymmetric pairs of fatty acids of 14, 16, or 18 carbons,
exhibit inhibition of surfactant secretion that correlates extremely well
with the phase transition temperature (Tc) of the phospholipid. The
inhibitory activity of dipalmitoylphosphatidylcholine is not dependent upon
lipid stereochemistry. N-Methylated derivatives of
dipalmitoylphosphatidylethanolamine are significantly less effective than
phosphatidylcholine as inhibitors. Phosphatidylcholines below their phase
transition temperature are inhibitors of surfactant secretion, whereas
those above their phase transition temperature are either ineffective or
weakly inhibitory. The phase transition dependence of inhibition is
observed when type II cells are incubated at 37 degrees C with different
species of phosphatidylcholine. In addition, if type II cells are
stimulated to secrete at different temperatures the efficacy of a given
phospholipid as an inhibitor is dependent on its relationship to Tc (i.e.
dipalmitoylphosphatidylcholine with a Tc of 41 degrees C significantly
inhibits secretion at 37 degrees C but not at 42 degrees C). Inhibition of
surfactant secretion by dipalmitoylphosphatidylcholine is abrogated when it
is incorporated into the same liposome with dioleoylphosphatidylcholine as
a 50:50 mixture. In contrast, the simultaneous addition of two separate
populations of liposomes, one composed of dipalmitoylphosphatidylcholine
and the other composed of dioleoylphosphatidylcholine, does not
significantly alter the inhibitory activity found with
dipalmitoylphosphatidylcholine alone. These data provide compelling
evidence that the physical state of phosphatidylcholine can regulate
surfactant secretion from alveolar type II cells and suggest a unique
mechanism for regulating exocytosis in the alveolus of the lung.
Pulmonary surfactant secretion is regulated by the physical state of extracellular phosphatidylcholine
Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, Denver, Colorado 80206.
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