z-logo
open-access-imgOpen Access
Theileria annulata promotes Src kinase‐dependent host cell polarization by manipulating actin dynamics in podosomes and lamellipodia
Author(s) -
Baumgartner Martin
Publication year - 2011
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 - 10.1111/j.1462-5822.2010.01553.x
Subject(s) - lamellipodium , podosome , biology , microbiology and biotechnology , moesin , radixin , ezrin , motility , actin , cell migration , cell , cytoskeleton , biochemistry
Summary Theileria annulata is an intracellular protozoan parasite that infects B cells and macrophages of ruminants. Macrophages infected with T. annulata are de‐differentiated and display tumour cell properties and a metastatic behaviour. How parasitized cells adapt their morphology, motility and invasive behaviour has not yet been addressed in detail. In this study, I investigated the regulation of host cell actin dynamics in T. annulata ‐transformed macrophages and how this affects host cell morphology and motility. T. annulata was found to promote the formation of filamentous‐actin‐rich podosome‐type adhesions (PTAs) and lamellipodia, and to establish a polarized morphology of the infected cell. Characteristic for parasite‐dependent host cell polarization is that infected cells display a single, persistent lamellipodium. Src kinases – in particular Hck – are required for the polar extension of this lamellipodium. Hck does so by promoting the clustered assembly of PTAs and accumulation of proteins of the Ezrin, Radixin, Moesin (ERM) family in lamellipodia. Polar accumulation of PTAs and ERM proteins correlates with focal matrix degradation underneath lamellipodia. These findings suggest that T. annulata equips its host cell with properties to adhere and invade. These properties are likely to promote the motile behaviour required for dissemination of infected cells in vivo .

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here