This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Furtado, G C
Right arrow Articles by Joiner, K A
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Furtado, G C
Right arrow Articles by Joiner, K A

 Previous Article  |  Next Article 

Infect Immun. 1992 November; 60(11): 4925-4931

Laminin on Toxoplasma gondii mediates parasite binding to the beta 1 integrin receptor alpha 6 beta 1 on human foreskin fibroblasts and Chinese hamster ovary cells.

G C Furtado, Y Cao and K A Joiner

Section of Infectious Disease, Yale University School of Medicine, New Haven, Connecticut 06510-8056.

ABSTRACT

We investigated the role of parasite-bound laminin and the host cell beta 1 integrin receptors for this extracellular matrix protein in Toxoplasma gondii binding to fibroblasts. Laminin but not fibronectin was detected on extracellular tachyzoites by immunofluorescence and immunoblotting. Binding of parasites to CHO cells was inhibited by polyclonal antibodies to laminin and by a monoclonal antibody directed against the globular carboxyl-terminal portion of the long arm of laminin (at or near the suggested ligand-binding sites for alpha 3 beta 1 and alpha 6 beta 1), but not by a monoclonal antibody directed against the lateral short arms of laminin near the cross region of the molecule. Antibodies to the alpha 6 but not the alpha 2, alpha 3, or alpha 5 chains of the beta 1 family of integrins blocked parasite attachment to human foreskin fibroblasts and CHO cells. Attachment of T. gondii to cells via laminin on the parasite surface and laminin receptors on the mammalian cell is consistent with the capacity of the parasite to invade almost all nucleated cells.


Infect Immun. 1992 November; 60(11): 4925-4931




This article has been cited by other articles:

  • Carter, C.J. (2009). Schizophrenia Susceptibility Genes Directly Implicated in the Life Cycles of Pathogens: Cytomegalovirus, Influenza, Herpes simplex, Rubella, and Toxoplasma gondii. Schizophr Bull 35: 1163-1182 [Abstract] [Full Text]  
  • Zamora, D O, Rosenbaum, J T, Smith, J R (2008). Invasion of human retinal vascular endothelial cells by Toxoplasma gondii tachyzoites. Br J Ophthalmol 92: 852-855 [Abstract] [Full Text]  
  • Cook, T., Roos, D., Morada, M., Zhu, G., Keithly, J. S., Feagin, J. E., Wu, G., Yarlett, N. (2007). Divergent polyamine metabolism in the Apicomplexa. Microbiology 153: 1123-1130 [Abstract] [Full Text]  
  • Bishop, J. R., Crawford, B. E., Esko, J. D. (2005). Cell Surface Heparan Sulfate Promotes Replication of Toxoplasma gondii. Infect. Immun. 73: 5395-5401 [Abstract] [Full Text]  
  • Coppens, I., Joiner, K. A. (2003). Host but Not Parasite Cholesterol Controls Toxoplasma Cell Entry by Modulating Organelle Discharge. Mol. Biol. Cell 14: 3804-3820 [Abstract] [Full Text]  
  • Dutta, C., Grimwood, J., Kasper, L. H. (2000). Attachment of Toxoplasma gondii to a Specific Membrane Fraction of CHO Cells. Infect. Immun. 68: 7198-7201 [Abstract] [Full Text]  
  • Black, M. W., Boothroyd, J. C. (2000). Lytic Cycle of Toxoplasma gondii. Microbiol. Mol. Biol. Rev. 64: 607-623 [Abstract] [Full Text]  
  • Carruthers, V. B., Hakansson, S., Giddings, O. K., Sibley, L. D. (2000). Toxoplasma gondii Uses Sulfated Proteoglycans for Substrate and Host Cell Attachment. Infect. Immun. 68: 4005-4011 [Abstract] [Full Text]  
  • Herron, M. J., Nelson, C. M., Larson, J., Snapp, K. R., Kansas, G. S., Goodman, J. L. (2000). Intracellular Parasitism by the Human Granulocytic Ehrlichiosis Bacterium Through the P-Selectin Ligand, PSGL-1. Science 288: 1653-1656 [Abstract] [Full Text]  
  • Klass, C., Couchman, J., Woods, A (2000). Control of extracellular matrix assembly by syndecan-2 proteoglycan. J. Cell Sci. 113: 493-506 [Abstract]  
  • Ortega-Barria, E., Boothroyd, J. C. (1999). A Toxoplasma Lectin-like Activity Specific for Sulfated Polysaccharides Is Involved in Host Cell Infection. J. Biol. Chem. 274: 1267-1276 [Abstract] [Full Text]