Open AccessLeishmania donovani lipophosphoglycan causes periphagosomal actin accumulation: correlation with impaired translocation of PKCα and defective phagosome maturation
Author(s) -
Holm Å.,
Tejle K.,
Magnusson K.E.,
Descoteaux A.,
Rasmusson B.
Publication year - 2001
Publication title -
cellular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.542
H-Index - 138
eISSN - 1462-5822
pISSN - 1462-5814
DOI - 10.1046/j.1462-5822.2001.00127.x
Subject(s) - lipophosphoglycan , phagosome , biology , leishmania donovani , phagocytosis , microbiology and biotechnology , nocodazole , leishmania , cytoskeleton , biochemistry , immunology , visceral leishmaniasis , cell , parasite hosting , leishmaniasis , world wide web , computer science
Lipophosphoglycan (LPG) is the major surface glycoconjugate of Leishmania donovani promastigotes. The repeating disaccharide–phosphate units of LPG are crucial for promastigote survival inside macrophages and establishment of infection. LPG has a number of effects on the host cell, including inhibition of PKC activity, inhibition of nitric oxide production and altered expression of cytokines. LPG also inhibits phagosomal maturation, a process requiring depolymerization of periphagosomal F‐actin. In the present study, we have characterized the dynamics of F‐actin during the phagocytosis of L. donovani promastigotes in J774 macrophages. We observed that F‐actin accumulated progressively around phagosomes containing wild‐type L. donovani promastigotes during the first hour of phagocytosis. Using LPG‐defective mutants and yeast particles coated with purified LPG, we obtained evidence that this effect could be attributed to the repeating units of LPG. LPG also disturbed cortical actin turnover during phagocytosis. The LPG‐dependent accumulation of periphagosomal F‐actin correlated with an impaired recruitment of the lysosomal marker LAMP1 and PKCα to the phagosome. Accumulation of periphagosomal F‐actin during phagocytosis of L. donovani promastigotes may contribute to the inhibition of phagosomal maturation by physically preventing vesicular trafficking to and from the phagosome.