Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1976 Nov 1;71(2):357–369. doi: 10.1083/jcb.71.2.357

Isolation and characterization of subcellular membranes of Entamoeba invadens

PMCID: PMC2109769  PMID: 136451

Abstract

A method is described for the isolation of subcellular membranes of Entamoeba invadens. Plasma membranes were obtained by rate centrifugation followed by isopycnic centrifugation on a sucrose gradient. Intact phagolysosomes floated in a 10% sucrose solution providing a simple technique for isolation. Phagolysosomal membranes were collected by isopycnic centrifugation, after lysis of the phagolysosomes. Microsomes were obtained by differential centrifugation. Membrane fractions were examined by electron microscopy, and the contamination of each fraction was determined with marker enzymes. Mg2+-ATPase is associated with the plasma membrane. Acid phosphatase (beta-glycerophosphate) was associated mainly with phagolysosmal membranes. Plasma membranes also contained acid phosphatase activity which hydrolyzes p-nitrophenylphosphate but not beta-glycerophosphate. The localization of the two phosphatases was confirmed cytochemically. Isolated plasma membranes were contaminated with phagolysosomal membranes (15%) and with microsomes (25%). No more than 5% of the phagolysosomal membrane fraction consisted of plasma membranes. Contamination of the microsomes by plasma and phagolysosomal membranes was 10% and 7%, respectively. Plasma membranes and phagolysosomal membranes had a high ratio of cholesterol to phospholipid (0.93 and 1.05 mumol/mumol, respectively). Microsomes were relatively poor in cholesterol (0.39 mumol/mumol). Microsomes, plasma, and phagolysosomal membranes contained increasing amounts of spingolipids (12%, 17%, and 28%). Phagolysosomal membranes had a high percentage of phosphatidylserine but little phosphatidylcholine. Microsomes were rich in phosphatidylcholine (45%). Differences in phospholipid composition between plasma and phagolysosomal membranes are discussed in view of the phagocytic process.

Full Text

The Full Text of this article is available as a PDF (2.3 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Aronson N. N., Jr, De Duve C. Digestive activity of lysosomes. II. The digestion of macromolecular carbohydrates by extracts of rat liver lysosomes. J Biol Chem. 1968 Sep 10;243(17):4564–4573. [PubMed] [Google Scholar]
  2. Barber A. J., Jamieson G. A. Isolation and characterization of plasma membranes from human blood platelets. J Biol Chem. 1970 Dec 10;245(23):6357–6365. [PubMed] [Google Scholar]
  3. Bretscher M. S. Phosphatidyl-ethanolamine: differential labelling in intact cells and cell ghosts of human erythrocytes by a membrane-impermeable reagent. J Mol Biol. 1972 Nov 28;71(3):523–528. doi: 10.1016/s0022-2836(72)80020-2. [DOI] [PubMed] [Google Scholar]
  4. Chlapowski F. J., Band R. N. Assembly of lipids into membranes in Acanthamoeba palestinensis. II. The origin and fate of glycerol- 3 H--labeled phospholipids of cellular membranes. J Cell Biol. 1971 Sep;50(3):634–651. doi: 10.1083/jcb.50.3.634. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DE DUVE C., WATTIAUX R. Tissue fractionation studies. VII. Release of bound hydrolases by means of triton X-100. Biochem J. 1956 Aug;63(4):606–608. doi: 10.1042/bj0630606. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. DEUTSCH K., ZAMAN V. An electron microscopic study of Entamoeba invadens Rodhain 1934. Exp Cell Res. 1959 May;17(2):310–319. doi: 10.1016/0014-4827(59)90222-8. [DOI] [PubMed] [Google Scholar]
  7. 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]
  8. Feria-Velasco A., TRevino N. The ultrastructure of trophozoites of Entamoeba histolytica with particular reference to spherical arrangements of osmiophilic cylindrical bodies. J Protozool. 1972 Feb;19(1):200–211. doi: 10.1111/j.1550-7408.1972.tb03436.x. [DOI] [PubMed] [Google Scholar]
  9. Fitzpatrick D. F., Davenport G. R., Forte L., Landon E. J. Characterization of plasma membrane proteins in mammalian kidney. I. Preparation of a membrane fraction and separation of the protein. J Biol Chem. 1969 Jul 10;244(13):3561–3569. [PubMed] [Google Scholar]
  10. GOLDBARG J. A., RUTENBURG A. M. The colorimetric determination of leucine aminopeptidase in urine and serum of normal subjects and patients with cancer and other diseases. Cancer. 1958 Mar-Apr;11(2):283–291. doi: 10.1002/1097-0142(195803/04)11:2<283::aid-cncr2820110209>3.0.co;2-8. [DOI] [PubMed] [Google Scholar]
  11. Gezelius K. Acid phosphatase localization during differentiation in the cellular slime mold Dictyostelium discoideum. Arch Mikrobiol. 1972;85(1):51–76. doi: 10.1007/BF00425144. [DOI] [PubMed] [Google Scholar]
  12. HIRSCH J. G., COHN Z. A. DIGESTIVE AND AUTOLYTIC FUNCTIONS OF LYSOSOMES IN PHAGOCYTIC CELLS. Fed Proc. 1964 Sep-Oct;23:1023–1025. [PubMed] [Google Scholar]
  13. Henning R., Kaulen H. D., Stoffel W. Biochemical analysis of the pinocytotic process. I. Isolation and chemical composition of the lysosomal and the plasma membrane of the rat liver cell. Hoppe Seylers Z Physiol Chem. 1970 Oct;351(10):1191–1199. doi: 10.1515/bchm2.1970.351.2.1191. [DOI] [PubMed] [Google Scholar]
  14. Kaulen H. D., Henning R., Stoffel W. Biochemical analsis of the inocytotic process. II. Comparison of some enzymes of the lysosomal nd the plasma membrane of the rat liver cel. Hoppe Seylers Z Physiol Chem. 1970 Dec;351(12):1555–1563. doi: 10.1515/bchm2.1970.351.2.1555. [DOI] [PubMed] [Google Scholar]
  15. Korn E. D. Cell membranes: structure and synthesis. Annu Rev Biochem. 1969;38:263–288. doi: 10.1146/annurev.bi.38.070169.001403. [DOI] [PubMed] [Google Scholar]
  16. Kress Y., Wittner M., Rosenbaum R. M. Sites of cytoplasmic ribonucleoprotein-filament assembly in relation to helical body formation in axenic trophozoites of Entamoeba histolytica. J Cell Biol. 1971 Jun;49(3):773–784. doi: 10.1083/jcb.49.3.773. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  18. Lowe C. Y., Maegraith B. G. Electron microscopy of Entamoeba histolytica in culture. Ann Trop Med Parasitol. 1970 Sep;64(3):283–291. doi: 10.1080/00034983.1970.11686693. [DOI] [PubMed] [Google Scholar]
  19. Lowe C. Y., Maegraith B. G. Electron microscopy of an axenic strain of Entamoeba histolytica. Ann Trop Med Parasitol. 1970 Sep;64(3):293–298. doi: 10.1080/00034983.1970.11686694. [DOI] [PubMed] [Google Scholar]
  20. Michell R. H., Hawthorne J. N. The site of diphosphoinositide synthesis in rat liver. Biochem Biophys Res Commun. 1965 Nov 22;21(4):333–338. doi: 10.1016/0006-291x(65)90198-1. [DOI] [PubMed] [Google Scholar]
  21. Nozawa Y., Thompson G. A., Jr Studies of membrane formation in Tetrahymena pyriformis. II. Isolation and lipid analysis of cell fractions. J Cell Biol. 1971 Jun;49(3):712–721. doi: 10.1083/jcb.49.3.712. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Proctor E. M., Gregory M. A. The observation of a surface active lysosome in the trophozoites of Entamoeba histolytica from the human colon. Ann Trop Med Parasitol. 1972 Sep;66(3):339–342. doi: 10.1080/00034983.1972.11686833. [DOI] [PubMed] [Google Scholar]
  23. Proctor E. M., Gregory M. A. The ultrastructure of axenically cultivated trophozoites of Entamoeba histolytica with particular reference to an observed variation in structural pattern. Ann Trop Med Parasitol. 1972 Sep;66(3):335–338. doi: 10.1080/00034983.1972.11686832. [DOI] [PubMed] [Google Scholar]
  24. Rosenbaum R. M., Wittner M. Ultrastructure of bacterized and axenic trophozoites of Entamoeba histolytica with particular reference to helical bodies. J Cell Biol. 1970 May;45(2):367–382. doi: 10.1083/jcb.45.2.367. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Rouser G., Fkeischer S., Yamamoto A. Two dimensional then layer chromatographic separation of polar lipids and determination of phospholipids by phosphorus analysis of spots. Lipids. 1970 May;5(5):494–496. doi: 10.1007/BF02531316. [DOI] [PubMed] [Google Scholar]
  26. Sarzala M. G., Van Golde L. M., De Kruyff B., Van Deenen L. L. The intramitochondrial distribution of some enzymes involved in the biosynthesis of rat-liver phospholipids. Biochim Biophys Acta. 1970 Feb 10;202(1):106–119. doi: 10.1016/0005-2760(70)90222-5. [DOI] [PubMed] [Google Scholar]
  27. Schultz T. M., Thompson J. E. Enrichment of 5'-nucleotidase in membrane fragments isolated from Acanthamoeba sp. Biochim Biophys Acta. 1969 Oct 14;193(1):203–211. doi: 10.1016/0005-2736(69)90073-x. [DOI] [PubMed] [Google Scholar]
  28. Spies F., Elbers P. F. Axenic mass cultivation of Entamoeba invadens and cell membrane isolation. J Protozool. 1972 Feb;19(1):102–107. doi: 10.1111/j.1550-7408.1972.tb03422.x. [DOI] [PubMed] [Google Scholar]
  29. Stossel T. P., Mason R. J., Pollard T. D., Vaughan M. Isolation and properties of phagocytic vesicles. II. Alveolar macrophages. J Clin Invest. 1972 Mar;51(3):604–614. doi: 10.1172/JCI106850. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Stossel T. P., Pollard T. D., Mason R. J., Vaughan M. Isolation and properties of phagocytic vesicles from polymorphonuclear leukocytes. J Clin Invest. 1971 Aug;50(8):1745–1747. doi: 10.1172/JCI106664. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Tsan M. F., Berlin R. D. Effect of phagocytosis on membrane transport of nonelectrolytes. J Exp Med. 1971 Oct 1;134(4):1016–1035. doi: 10.1084/jem.134.4.1016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Ulsamer A. G., Wright P. L., Wetzel M. G., Korn E. D. Plasma and phagosome membranes of Acanthamoeba castellanii. J Cell Biol. 1971 Oct;51(1):193–215. doi: 10.1083/jcb.51.1.193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Van Golde L. M., Fleischer B., Fleischer S. Some studies on the metabolism of phospholipids in Golgi complex from bovine and rat liver in comparison to other subcellular fractions. Biochim Biophys Acta. 1971 Oct 12;249(1):318–330. doi: 10.1016/0005-2736(71)90109-x. [DOI] [PubMed] [Google Scholar]
  34. Widnell C. C., Unkeless J. C. Partial purification of a lipoprotein with 5'-nucleotidase activity from membranes of rat liver cells. Proc Natl Acad Sci U S A. 1968 Nov;61(3):1050–1057. doi: 10.1073/pnas.61.3.1050. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Zwaal R. F., Roelofsen B., Colley C. M. Localization of red cell membrane constituents. Biochim Biophys Acta. 1973 Sep 10;300(2):159–182. doi: 10.1016/0304-4157(73)90003-8. [DOI] [PubMed] [Google Scholar]
  36. van Blitterswijk W. J., Emmelot P., Feltkamp C. A. Studies on plasma membranes. XIX. Isolation and characterization of a plasma membrane fraction from calf thymocytes. Biochim Biophys Acta. 1973 Mar 29;298(3):577–592. doi: 10.1016/0005-2736(73)90075-8. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES