The Journal of Experimental Medicine
Torrey Pines Biolabs
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents
This Article
Right arrow Full Text
Right arrow Full Text (PDF, 1067K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Right arrow Citation Map
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new content in the JEM
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Desjardins, M.
Right arrow Articles by Descoteaux, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Desjardins, M.
Right arrow Articles by Descoteaux, A.
Social Bookmarking
Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?
© The Rockefeller University Press, 0022-1007/1997/6/2061/ $5.00
The Journal of Experimental Medicine, Volume 185, Number 12, June 16, 1997 2061-2068

Articles

Inhibition of Phagolysosomal Biogenesis by the Leishmania Lipophosphoglycan

Michel Desjardins* and Albert Descoteaux{ddagger}

From the * Département d'anatomie,Université de Montréal, Montréal, Québec, Canada, H3C 3J7; and the {ddagger} Institut Armand-Frappier, Centre de recherche en immunologie, Laval, Québec, Canada H7N 4Z3

Whereas amastigotes of the protozoan parasite Leishmania proliferate inside acidic phagolysosomal vacuoles of the macrophage, vacuoles induced by Leishmania donovani promastigotes during initiation of infection are poorly characterized. Here, evidence is presented that interaction of these parasitophorous vacuoles with endocytic organelles is very limited. In contrast, vacuoles formed around L. donovani mutants lacking the cell surface lipophosphoglycan (LPG) fuse extensively with endosomes and lysosomes. The role of LPG repeating units in the inhibition of phagosome–endosome fusion was demonstrated using two different approaches. First, genetic complementation of the LPG-defective C3PO mutant restored its ability to inhibit phagosome–endosome fusion to a degree similar to that of wild-type promastigotes. Second, opsonization of C3PO mutant cells with purified L. donovani LPG also conferred to this mutant the ability to inhibit phagosome–endosome fusion. Inasmuch as LPG is essential for infecting macrophages, these results suggest that inhibition of phagolysosomal biogenesis by LPG repeating units represents an intramacrophage survival strategy used by promastigotes to establish infection.

Address correspondence to A. Descoteaux at the Institut Armand-Frappier, Centre de recherche en immunologie, 531 boulevard des Prairies, CP100, Laval, Québec, Canada H7N 4Z3, Phone: 514-686-5332; FAX: 514-685-5501; E-mail: albert_descoteaux@iaf.uquebec.ac, or to M. Desjardins at the Département d'anatomie, Université de Montréal, CP6128 Succ. Centre Ville, Montréal, Québec, Canada H3C3J7, Phone: 514-343-7350; FAX: 514-343-2459; E-mail: desjarm{at}ere.umontreal.ca

1Abbreviations used in this paper: LPG, lipophosphogylcan; GPI, glycosylinositolphospholipid; PKC, protein kinase C; WT, wild-type.


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:



  Home | Help | Feedback | Subscriptions | Archive | Search
TABLE OF CONTENTS