Regulatory mechanisms of surfactant secretion

被引:87
作者
Mason, RJ
Voelker, DR
机构
[1] Natl Jewish Med & Res Ctr, Dept Med, Denver, CO 80206 USA
[2] Univ Colorado, Dept Med, Denver, CO USA
[3] Univ Colorado, Dept Biochem, Denver, CO 80202 USA
[4] Natl Jewish Med & Res Ctr, Lord & Taylor Lab Lung Biochem, Denver, CO USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 1998年 / 1408卷 / 2-3期
关键词
dipalmitoylphosphatidylcholine; alveolar type II cell; surfactant protein; SP-A; SP-B; SP-C; SP-D; exocytosis;
D O I
10.1016/S0925-4439(98)00070-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Surfactant secretion is a critical regulated process in the metabolism of pulmonary surfactant. Presumably, because this process is vital to the survival of the organism, there are several independent pathways for stimulating secretion which work through different cell surface receptors and signaling mechanisms. In addition, there is apparent homeostatic regulation in that two components of surfactant, namely SP-A and dipalmitoylphosphatidylcholine, can inhibit secretion. Although secretion of surfactant has been studied for over two decades, there remains some important issues to be resolved. In vivo secretion can be stimulated by hyperventilation or even a single large breath. However, we do not know the biochemical mechanism for this physiologically important form of stimulation. In vitro, we know many of the proximal events in signaling, but we do not know how the lamellar bodies move within a cell or the docking mechanism at the plasma membrane. Many investigators have demonstrated that SP-A will inhibit secretion in vitro, but the mechanism is not known. Finally, there is a route of secretion of SP-A independent of lamellar bodies, but we do not know details of this pathway nor its regulation. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:226 / 240
页数:15
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