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. 1987 Mar;55(3):736–741. doi: 10.1128/iai.55.3.736-741.1987

Phospholipid profile of Pneumocystis carinii and its interaction with alveolar type II epithelial cells.

E L Pesanti
PMCID: PMC260403  PMID: 3493222

Abstract

Pneumocystis carinii is an obligate parasite of mammalian lungs, attaching to but not invading the alveolar epithelium. The alveolar air spaces are rich in phospholipids, which are secreted by steroid-responsive alveolar type II epithelial cells. P. carinii isolated from rat lungs was found to contain the expected structural phospholipids as well as a large amount of firmly attached disaturated phosphatidylcholine, the characteristic phospholipid of alveolar surfactant. In vitro, P. carinii cells synthesized phospholipids from simple radiolabeled precursors; disaturated phosphatidylcholine was not formed. However, washed P. carinii cells avidly adsorbed radiolabeled rat surfactant, a process that appeared to be saturable, not dependent on viability of the organisms, and abolished by incubation at 4 degrees C. The surfactant was neither harmful nor beneficial to in vitro survival of the organisms. With the exception of high concentrations of arachidonic acid, fatty acids found in rat alveolar lining material were also not toxic. In addition, cultures consisting primarily of rat type II alveolar epithelial cells were toxic to P. carinii when the organisms were added to monolayers of type II cells at less than or equal to 10:1 multiplicity. At higher multiplicities, the parasite survived (but did not increase in numbers), and the type II cells deteriorated. The mechanism for this effect has not been determined.

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Selected References

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  1. Bloom B. R. Games parasites play: how parasites evade immune surveillance. Nature. 1979 May 3;279(5708):21–26. doi: 10.1038/279021a0. [DOI] [PubMed] [Google Scholar]
  2. Coonrod J. D., Lester R. L., Hsu L. C. Characterization of the extracellular bactericidal factors of rat alveolar lining material. J Clin Invest. 1984 Oct;74(4):1269–1279. doi: 10.1172/JCI111537. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cushion M. T., Ruffolo J. J., Linke M. J., Walzer P. D. Pneumocystis carinii: growth variables and estimates in the A549 and WI-38 VA13 human cell lines. Exp Parasitol. 1985 Aug;60(1):43–54. doi: 10.1016/s0014-4894(85)80021-7. [DOI] [PubMed] [Google Scholar]
  4. Cushion M. T., Walzer P. D. Growth and serial passage of Pneumocystis carinii in the A549 cell line. Infect Immun. 1984 May;44(2):245–251. doi: 10.1128/iai.44.2.245-251.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. FOLCH J., LEES M., SLOANE STANLEY G. H. A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem. 1957 May;226(1):497–509. [PubMed] [Google Scholar]
  6. Gross I., Wilson C. M., Ingleson L. D., Brehier A., Rooney S. A. The influence of hormones on the biochemical development of fetal rat lung in organ culture. I. Estrogen. Biochim Biophys Acta. 1979 Dec 18;575(3):375–383. doi: 10.1016/0005-2760(79)90106-1. [DOI] [PubMed] [Google Scholar]
  7. Gross N. J. Radiation pneumonitis in mice. Some effects of corticosteroids on mortality and pulmonary physiology. J Clin Invest. 1980 Sep;66(3):504–510. doi: 10.1172/JCI109881. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gross N. J., Smith D. M. Methylprednisolone increases the toxicity of oxygen in adult mice. Mechanical and biochemical effects on the surfactant system. Am Rev Respir Dis. 1984 May;129(5):805–810. doi: 10.1164/arrd.1984.129.5.805. [DOI] [PubMed] [Google Scholar]
  9. Hernell O., Ward H., Bläckberg L., Pereira M. E. Killing of Giardia lamblia by human milk lipases: an effect mediated by lipolysis of milk lipids. J Infect Dis. 1986 Apr;153(4):715–720. doi: 10.1093/infdis/153.4.715. [DOI] [PubMed] [Google Scholar]
  10. Höltje J. V., Tomasz A. Lipoteichoic acid: a specific inhibitor of autolysin activity in Pneumococcus. Proc Natl Acad Sci U S A. 1975 May;72(5):1690–1694. doi: 10.1073/pnas.72.5.1690. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kernbaum S., Masliah J., Alcindor L. G., Bouton C., Christol D. Phospholipase activities of bronchoalveolar lavage fluid in rat Pneumocystis carinii pneumonia. Br J Exp Pathol. 1983 Feb;64(1):75–80. [PMC free article] [PubMed] [Google Scholar]
  12. King R. J., Clements J. A. Surface active materials from dog lung. I. Method of isolation. Am J Physiol. 1972 Sep;223(3):707–714. doi: 10.1152/ajplegacy.1972.223.3.707. [DOI] [PubMed] [Google Scholar]
  13. Kotas R. V., Avery M. E. The influence of sex on fetal rabbit lung maturation and on the response to glucocorticoid. Am Rev Respir Dis. 1980 Feb;121(2):377–380. doi: 10.1164/arrd.1980.121.2.377. [DOI] [PubMed] [Google Scholar]
  14. Lanken P. N., Minda M., Pietra G. G., Fishman A. P. Alveolar response to experimental Pneumocystis carinii pneumonia in the rat. Am J Pathol. 1980 Jun;99(3):561–588. [PMC free article] [PubMed] [Google Scholar]
  15. Leslie C. C., McCormick-Shannon K., Cook J. L., Mason R. J. Macrophages stimulate DNA synthesis in rat alveolar type II cells. Am Rev Respir Dis. 1985 Dec;132(6):1246–1252. doi: 10.1164/arrd.1985.132.6.1246. [DOI] [PubMed] [Google Scholar]
  16. Mason R. J., Nellenbogen J., Clements J. A. Isolation of disaturated phosphatidylcholine with osmium tetroxide. J Lipid Res. 1976 May;17(3):281–284. [PubMed] [Google Scholar]
  17. Mason R. J., Williams M. C., Greenleaf R. D., Clements J. A. Isolation and properties of type II alveolar cells from rat lung. Am Rev Respir Dis. 1977 Jun;115(6):1015–1026. doi: 10.1164/arrd.1977.115.6.1015. [DOI] [PubMed] [Google Scholar]
  18. Masur H., Jones T. C. The interaction in vitro of Pneumocystis carinii with macrophages and L-cells. J Exp Med. 1978 Jan 1;147(1):157–170. doi: 10.1084/jem.147.1.157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Pesanti E. L., Cox C. Metabolic and synthetic activities of Pneumocystis carinii in vitro. Infect Immun. 1981 Dec;34(3):908–914. doi: 10.1128/iai.34.3.908-914.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Pesanti E. L. Effects of bacterial pneumonitis on development of pneumocystosis in rats. Am Rev Respir Dis. 1982 Jun;125(6):723–726. doi: 10.1164/arrd.1982.125.6.723. [DOI] [PubMed] [Google Scholar]
  21. Pesanti E. L. In vitro effects of antiprotozoan drugs and immune serum on Pneumocystis carinii. J Infect Dis. 1980 Jun;141(6):775–780. doi: 10.1093/infdis/141.6.775. [DOI] [PubMed] [Google Scholar]
  22. Pesanti E. L. Pneumocystis carinii: oxygen uptake, antioxidant enzymes, and susceptibility to oxygen-mediated damage. Infect Immun. 1984 Apr;44(1):7–11. doi: 10.1128/iai.44.1.7-11.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Picken J., Lurie M., Kleinerman J. Mechanical and morphologic effects of long-term corticosteroid administration on the rat lung. Am Rev Respir Dis. 1974 Dec;110(6):746–753. doi: 10.1164/arrd.1974.110.6P1.746. [DOI] [PubMed] [Google Scholar]
  24. Robinson P. C., Voelker D. R., Mason R. J. Isolation and culture of human alveolar type II epithelial cells. Characterization of their phospholipid secretion. Am Rev Respir Dis. 1984 Dec;130(6):1156–1160. doi: 10.1164/arrd.1984.130.6.1156. [DOI] [PubMed] [Google Scholar]
  25. Rooney S. A. The surfactant system and lung phospholipid biochemistry. Am Rev Respir Dis. 1985 Mar;131(3):439–460. doi: 10.1164/arrd.1985.131.3.439. [DOI] [PubMed] [Google Scholar]
  26. Rouser G., Siakotos A. N., Fleischer S. Quantitative analysis of phospholipids by thin-layer chromatography and phosphorus analysis of spots. Lipids. 1966 Jan;1(1):85–86. doi: 10.1007/BF02668129. [DOI] [PubMed] [Google Scholar]
  27. Smith L. J., Brody J. S. Influence of methylprednisolone on mouse alveolar type 2 cell response to acute lung injury. Am Rev Respir Dis. 1981 Apr;123(4 Pt 1):459–464. doi: 10.1164/arrd.1981.123.4.459. [DOI] [PubMed] [Google Scholar]
  28. Van Golde L. M. Metabolism of phospholipids in the lung. Am Rev Respir Dis. 1976 Nov;114(5):977–1000. doi: 10.1164/arrd.1976.114.5.977. [DOI] [PubMed] [Google Scholar]
  29. Von Behren L. A., Pesanti E. L. Uptake and degradation of Pneumocystis carinii by macrophages in vitro. Am Rev Respir Dis. 1978 Dec;118(6):1051–1059. doi: 10.1164/arrd.1978.118.6.1051. [DOI] [PubMed] [Google Scholar]

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