|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
Journal of Cell Science, Vol 92, Issue 4 691-699, Copyright © 1989 by Company of Biologists
JOURNAL ARTICLES |
AR Dluzewski, PR Fryer, S Griffiths, RJ Wilson and WB Gratzer
Medical Research Council Cell Biophysics Unit, King's College, London, UK.
Immuno-gold labelling electron microscopy of thin sections was used to determine the distribution of red cell membrane and membrane skeleton proteins in the vicinity of internalized malaria parasites. When examined immediately after invasion (young ring-stage parasites), the parasitophorous vacuole membranes of both Plasmodium falciparum and P. knowlesi were found to be characterized by the essentially complete absence of spectrin, ankyrin and the most abundant transmembrane protein, band 3. P. knowlesi merozoites were trapped in the attached but not internalized state by pretreatment with cytochalasin B. In this merozoite-red cell complex antibody labelling showed that band 3 had been eliminated from the region of the host cell membrane in contact with the parasite. Internal vesicles, originating apparently from the site of attachment, were often observed in the red cell. Opposite the attached parasite a cavity was also sometimes seen in the host cell, presumably representing an incipient internal vesicle. The membrane was intact, as judged by the absence of protein (haemoglobin) in the cavity, and, like the membranes surrounding the internal vesicles, was devoid of membrane proteins. A large multilamellar body was sometimes seen in the merozoite close to its point of attachment. The lamellar spacing was about 50 nm. The electron microscope images suggest a diffusion of electron-dense material from the lamellar body into the cavity in the host cell.
This article has been cited by other articles:
![]() |
C. D. Fitch and N. V. Russell Accelerated denaturation of hemoglobin and the antimalarial action of chloroquine. Antimicrob. Agents Chemother., July 1, 2006; 50(7): 2415 - 2419. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. E. Topolska, A. Lidgett, D. Truman, H. Fujioka, and R. L. Coppel Characterization of a Membrane-associated Rhoptry Protein of Plasmodium falciparum J. Biol. Chem., February 6, 2004; 279(6): 4648 - 4656. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Kirk Membrane Transport in the Malaria-Infected Erythrocyte Physiol Rev, April 1, 2001; 81(2): 495 - 537. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Pinder, R. Fowler, A. Dluzewski, L. Bannister, F. Lavin, G. Mitchell, R. Wilson, and W. Gratzer Actomyosin motor in the merozoite of the malaria parasite, Plasmodium falciparum: implications for red cell invasion J. Cell Sci., January 7, 1998; 111(13): 1831 - 1839. [Abstract] [PDF] |
||||
![]() |
K Lingelbach and K. Joiner The parasitophorous vacuole membrane surrounding Plasmodium and Toxoplasma: an unusual compartment in infected cells J. Cell Sci., January 6, 1998; 111(11): 1467 - 1475. [Abstract] [PDF] |
||||
![]() |
G. Ward, L. Miller, and J. Dvorak The origin of parasitophorous vacuole membrane lipids in malaria-infected erythrocytes J. Cell Sci., January 9, 1993; 106(1): 237 - 248. [Abstract] [PDF] |
||||