Alveolar surfactant is a mixture of lipids, proteins, and carbohydrates, which is synthesized in alveolar type II cells where it is stored in lamellar bodies until it is secreted into the alveoli. Its main function is to reduce surface tension in the lungs. An inadequate amount of functional surfactant, such as occurs in the respiratory distress syndrome of the newborn, results in impaired gas exchange. Although the synthesis and secretion of surfactant have been extensively studied, far less is known about its intra-alveolar metabolism and clearance. Available data suggest that a major route for clearance is the uptake of surfactant phospholipids by type II cells. The principal goal of the proposed work is to study the mechanisms involved in surfactant uptake. Studies performed in this laboratory over the past few years suggest that subfractions of surfactant, which are obtained by differential centrifugation of lavage fluid and which have different physical and biochemical properties, are taken up from the alveoli into lamellar bodies of type II cells at different rates. The two fractions which were most rapidly taken up contained the major surfactant apoprotein (apo 36), large multilamellar vesicles and tubular myelin, and they were highly surface active. The other major surfactant apoprotein group, apo 10, was present in only one of the fractions. The more slowly taken up fraction contained very little apoprotein or tubular myelin and was minimally surface active. I am proposing that there is a specific mechanism of uptake, mediated by some property of the rapidly taken up fractions. The experiments I am proposing to test this hypothesis are directed at 3 specific aims. 1) I will determine which properties of the preferentially taken up subfractions are responsible for their increased uptake. I will determine if apo 36 or some other property, determined by using better purified fractions, augment uptake of phospholipids by isolated type II cells. 2) I will determine if proteins are internalized and I will study the metabolism of lipids and proteins after uptake. Phospholipids will be analyzed by thin-layer chromatography; proteins will be analyzed by slab gel electrophoresis. 3) I will attempt to determine the mechanism of uptake (i.e. endocytosis, fusion or lipid transfer).

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
2R01HL030923-04
Application #
3341925
Study Section
Respiratory and Applied Physiology Study Section (RAP)
Project Start
1983-07-01
Project End
1989-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
4
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Holmer, Stephanie M; Evans, Kathy S; Asfaw, Yohannes G et al. (2014) Impact of surfactant protein D, interleukin-5, and eosinophilia on Cryptococcosis. Infect Immun 82:683-93
Perfect, John R (2014) Cryptococcosis: a model for the understanding of infectious diseases. J Clin Invest 124:1893-5
Mukherjee, Sambuddho; Giamberardino, Charles; Thomas, Joseph M et al. (2012) Surfactant protein A modulates induction of regulatory T cells via TGF-?. J Immunol 188:4376-84
Geunes-Boyer, Scarlett; Beers, Michael F; Perfect, John R et al. (2012) Surfactant protein D facilitates Cryptococcus neoformans infection. Infect Immun 80:2444-53
Mukherjee, Sambuddho; Giamberardino, Charles; Thomas, Joseph et al. (2012) Surfactant protein A integrates activation signal strength to differentially modulate T cell proliferation. J Immunol 188:957-67
Ledford, Julie G; Pastva, Amy M; Wright, Jo Rae (2010) Review: Collectins link innate and adaptive immunity in allergic airway disease. Innate Immun 16:183-90
Geunes-Boyer, Scarlett; Heitman, Joseph; Wright, Jo Rae et al. (2010) Surfactant protein D binding to Aspergillus fumigatus hyphae is calcineurin-sensitive. Med Mycol 48:580-8
Geunes-Boyer, Scarlett; Oliver, Timothy N; Janbon, Guilhem et al. (2009) Surfactant protein D increases phagocytosis of hypocapsular Cryptococcus neoformans by murine macrophages and enhances fungal survival. Infect Immun 77:2783-94
Lord, Christopher A; Savitsky, David; Sitcheran, Raquel et al. (2009) Blimp-1/PRDM1 mediates transcriptional suppression of the NLR gene NLRP12/Monarch-1. J Immunol 182:2948-58
Zaas, David W; Swan, Zachary D; Brown, Bethany J et al. (2009) Counteracting signaling activities in lipid rafts associated with the invasion of lung epithelial cells by Pseudomonas aeruginosa. J Biol Chem 284:9955-64

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