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Pulmonary surfactant and its components inhibit secretion of phosphatidylcholine from cultured rat alveolar type II cells

TLDR
Findings that suggest that surfactant inhibits secretion of 3H-labeled phosphatidylcholine by cultured rat type II cells are compatible with the hypothesis that Surfactant secretion is under feedback regulatory control.
Abstract
Pulmonary surfactant is synthesized and secreted by alveolar type II cells. Radioactive phosphatidylcholine has been used as a marker for surfactant secretion. We report findings that suggest that surfactant inhibits secretion of 3H-labeled phosphatidylcholine by cultured rat type II cells. The lipid components and the surfactant protein group of Mr 26,000-36,000 (SP 26-36) inhibit secretion to different extents. Surfactant lipids do not completely inhibit release; in concentrations of 100 micrograms/ml, lipids inhibit stimulated secretion by 40%. SP 26-36 inhibits release with an EC50 of 0.1 microgram/ml. At concentrations of 1.0 microgram/ml, SP 26-36 inhibits basal secretion and reduces to basal levels secretion stimulated by terbutaline, phorbol 12-myristate 13-acetate, and the ionophore A23187. The inhibitory effect of SP 26-36 can be blocked by washing type II cells after adding SP 26-36, by heating the proteins to 100 degrees C for 10 min, by adding antiserum specific to SP 26-36, or by incubating cells in the presence of 0.2 mM EGTA. SP 26-36 isolated from canine and human sources also inhibits phosphatidylcholine release from rat type II cells. Neither type I collagen nor serum apolipoprotein A-1 inhibits secretion. These findings are compatible with the hypothesis that surfactant secretion is under feedback regulatory control.

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Citations
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Alveolar epithelial type II cell: defender of the alveolus revisited

TL;DR: Controversy about the character of hyperplastic AE2 cells, reported to synthesise profibrotic factors, proscribes drawing a definite conclusion today.
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Surfactant and the Adult Respiratory Distress Syndrome

TL;DR: With further clinical trials and continued research efforts, exogenous surfactant administration should play a useful role in the future therapeutic approach to patients with ARDS.
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Calcium mobilization and exocytosis after one mechanical stretch of lung epithelial cells.

TL;DR: Mechanical factors can trigger complex cellular events in nonneuron, nonmuscle cells and may be involved in regulating normal lung functions by stimulating type II cells to secrete surfactant.
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Function and regulation of expression of pulmonary surfactant-associated proteins.

TL;DR: Structural characterization of 8-crystallin with enzymic activity and identification of valine/leucine/isoleucine and threonine/alanine/ glycine proton-spin systems of Escherichia coli adenylate kinase by selective deuteration and selective protonation are reported.
References
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Protein Measurement with the Folin Phenol Reagent

TL;DR: Procedures are described for measuring protein in solution or after precipitation with acids or other agents, and for the determination of as little as 0.2 gamma of protein.
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

TL;DR: Using an improved method of gel electrophoresis, many hitherto unknown proteins have been found in bacteriophage T4 and some of these have been identified with specific gene products.
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A simple method for the isolation and purification of total lipides from animal tissues.

TL;DR: In this paper, the authors described a simplified version of the method and reported the results of a study of its application to different tissues, including the efficiency of the washing procedure in terms of the removal from tissue lipides of some non-lipide substances of special biochemical interest.
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A simple technique for eliminating interference by detergents in the Lowry method of protein determination.

TL;DR: The addition of 0.5% sodium dodecylsulphate in the alkali reagent prevented this precipitation without affecting colour development, and allowed the Lowry method to be used on detergent treated membrane preparations.
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Primary culture of parenchymal liver cells on collagen membranes. Morphological and biochemical observations.

TL;DR: Comparative morphological and biochemical studies of primary cultures of parenchymal liver cells from adult rat liver cultured on collagen-coated plates and floating collagen membranes indicate that the latter have a markedly prolonged viability and show Morphological and functional features reminiscent of liver in vivo.
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