Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1983 Aug 1;97(2):317–322. doi: 10.1083/jcb.97.2.317

Acanthamoeba discriminates internally between digestible and indigestible particles

PMCID: PMC2112535  PMID: 6350315

Abstract

The capacity of Acanthamoeba to distinguish nutritive yeast particles from non-nutritive plastic beads during phagocytosis was investigated. When cells were allowed to phagocytose yeast to capacity, endocytosis stopped and subsequent presentation of particles (either yeast or beads) did not result in further uptake. By contrast, when cells were allowed to phagocytose plastic beads to capacity and a second dose of particles was presented (either yeast or beads), the cells exocytosed the internal particles and took up new ones. Yeast rendered indigestible by extensive chemical cross-linking were taken up at rates similar to those of untreated yeast, but, like beads, they were exocytosed when a second dose of particles was presented. The results show that an internal distinction is made between vacuoles containing yeast and vacuoles containing plastic beads, and they are consistent with the hypothesis that the presence within the vacuoles of material capable of being digested prevents exocytosis.

Full Text

The Full Text of this article is available as a PDF (1.6 MB).

Selected References

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

  1. Bowers B. A morphological study of plasma and phagosome membranes during endocytosis in Acanthamoeba. J Cell Biol. 1980 Feb;84(2):246–260. doi: 10.1083/jcb.84.2.246. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bowers B. Comparison of pinocytosis and phagocytosis in Acanthamoeba castellanii. Exp Cell Res. 1977 Dec;110(2):409–417. doi: 10.1016/0014-4827(77)90307-x. [DOI] [PubMed] [Google Scholar]
  3. Bowers B., Olszewski T. E., Hyde J. Morphometric analysis of volumes and surface areas in membrane compartments during endocytosis in Acanthamoeba. J Cell Biol. 1981 Mar;88(3):509–515. doi: 10.1083/jcb.88.3.509. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Brown R. C., Bass H., Coombs J. P. Carbohydrate binding proteins involved in phagocytosis by Acanthamoeba. Nature. 1975 Apr 3;254(5499):434–435. doi: 10.1038/254434a0. [DOI] [PubMed] [Google Scholar]
  5. Chapman-Andresen C., Christensen S. Pinocytic uptake of ferritin by the amoeba Chaos chaos measured by atomic absorption of iron. C R Trav Lab Carlsberg. 1970;38(2):19–57. [PubMed] [Google Scholar]
  6. Chapman-Andresen C., Nilsson J. R. Studies on endocytosis in amoebae. The distribution of pinocytically ingested dyes in relation to food vacuoles in Chaos chaos. II. Electron microscopic observations using alcian blue. C R Trav Lab Carlsberg. 1967;36(9):189–207. [PubMed] [Google Scholar]
  7. Hellio R., Ryter A. Relationships between anionic sites and lectin receptors in the plasma membrane of Dictyostelium discoideum and their role in phagocytosis. J Cell Sci. 1980 Feb;41:89–104. doi: 10.1242/jcs.41.1.89. [DOI] [PubMed] [Google Scholar]
  8. Hohman T. C., McNeil P. L., Muscatine L. Phagosome-lysosome fusion inhibited by algal symbionts of Hydra viridis. J Cell Biol. 1982 Jul;94(1):56–63. doi: 10.1083/jcb.94.1.56. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Oates P. J., Touster O. In vitro fusion of Acanthamoeba phagolysosomes. I. Demonstration and quantitation of vacuole fusion in Acanthamoeba homogenates. J Cell Biol. 1976 Feb;68(2):319–338. doi: 10.1083/jcb.68.2.319. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Rabinovitch M., De Stefano M. J. Phagocytosis of erythrocytes by Acanthamoeba sp. Exp Cell Res. 1971 Feb;64(2):275–284. doi: 10.1016/0014-4827(71)90077-2. [DOI] [PubMed] [Google Scholar]
  11. Ryter A., Bowers B. Localization of acid phosphatase in Acanthamoeba castellanii with light and electron microscopy during growth and after phagocytosis. J Ultrastruct Res. 1976 Dec;57(3):309–321. doi: 10.1016/s0022-5320(76)80119-0. [DOI] [PubMed] [Google Scholar]
  12. Silverstein S. C., Steinman R. M., Cohn Z. A. Endocytosis. Annu Rev Biochem. 1977;46:669–722. doi: 10.1146/annurev.bi.46.070177.003321. [DOI] [PubMed] [Google Scholar]
  13. Stewart W. W. Lucifer dyes--highly fluorescent dyes for biological tracing. Nature. 1981 Jul 2;292(5818):17–21. doi: 10.1038/292017a0. [DOI] [PubMed] [Google Scholar]
  14. Vogel G., Thilo L., Schwarz H., Steinhart R. Mechanism of phagocytosis in Dictyostelium discoideum: phagocytosis is mediated by different recognition sites as disclosed by mutants with altered phagocytotic properties. J Cell Biol. 1980 Aug;86(2):456–465. doi: 10.1083/jcb.86.2.456. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Weisman R. A., Korn E. D. Phagocytosis of latex beads by Acanthamoeba. I. Biochemical properties. Biochemistry. 1967 Feb;6(2):485–497. doi: 10.1021/bi00854a017. [DOI] [PubMed] [Google Scholar]
  16. Wetzel M. G., Korn E. D. Phagocytosis of latex beads by Acahamoeba castellanii (Neff). 3. Isolation of the phagocytic vesicles and their membranes. J Cell Biol. 1969 Oct;43(1):90–104. doi: 10.1083/jcb.43.1.90. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES