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Revealing Annexin A2 and ARF-6 enrollment during Trypanosoma cruzi extracellular amastigote-host cell interaction
© Teixeira et al. 2015
- Received: 28 May 2015
- Accepted: 15 September 2015
- Published: 29 September 2015
Invasion of host cells by Trypanosoma cruzi extracellular amastigotes is host actin polymerization-dependent. However, the role of proteins related to actin dynamics during invasion by amastigotes remains to be investigated. Here we describe the role of Annexin A2 and ARF-6 during extracellular amastigote-mammalian cell interactions.
Our results showed ARF-6 accumulation in the amastigote-containing parasitophorous vacuole containing amastigote forms; demonstrated ARF-6 and Annexin A2 critical impact over parasite cell invasion and revealed the effect of Annexin A2 expression on intracellular parasite multiplication.
ARF-6 and Annexin A2 are involved in invasion of mammalian cells by T. cruzi amastigotes.
- Trypanosoma cruzi
- Extracellular amastigotes
- Annexin A2
- Cell invasion
- Actin cytoskeleton
The Annexin family proteins are implicated in a wide range of cellular responses triggered by increased cytoplasmatic calcium levels . Annexin A2 has an essential role in actin-based macropinocytic rocketing  and is expressed at the interface between F-actin and membranes enriched in phosphatidylinositol 4,5,-biphosphate (PIP2) . Moreover, Annexin A2 is recruited to membrane structures enriched in F-actin during enterophatogenic Escherichia coli host cell adhesion .
The ARF family of small GTPases regulates membrane trafficking and actin cytoskeleton rearrangements . ADP-ribosylation factor 6 (ARF-6) participates during Chlamydia caviae and Yersinia pseudotuberculosis host cell invasion by acting on actin cytoskeleton polymerization [6–8]. In this context, ARF-6 showed an important role during Toxoplasma gondii cell invasion activating PI3-kinase signaling pathway and mobilizing PIP2 and PIP3 to the parasite parasitophorous vacuole .
Invasion of host cells by Trypanosoma cruzi extracellular amastigotes (EA) is host actin polymerization-dependent. EAs induce the formation of crater or cup-like structures enriched in F-actin reliant on host cell type . Here we aimed to study the role of actin polymerization-related proteins, Annexin A2 and ARF-6, during EA host cell interaction in vitro.
Although not a common property within the annexin family, several annexins have been shown to interact directly with polymerized actin in vitro, which correlates with the functions that have been proposed for these annexins in mediating, stabilizing and/or regulating membrane–actin interactions . Annexin A2, both as a monomer or in the heterotetrameric complex with S100A10, was the first annexin shown to be capable of binding to and also bundling actin filaments in a Ca2+-dependent manner . Despite its ability to bundle actin filaments, annexin A2 is not found to be associated with prominent actin bundles or cables within cells, such as microvilli or stress fibers. However, more dynamic actin structures, in particular those associated with cellular membranes during phagocytosis, pinocytosis and cell migration contain annexin 2 . Annexin A2 participates in lipid raft formation  and is a PIP2-interacting protein, thereby explaining its affinity to lipid membranes . Taken together, it has been shown that T. cruzi EAs induce host cell calcium signaling  and mobilize lipid raft domains during host cell invasion .
Authors have shown that Annexin A2 functions as a platform for actin remodeling in the vicinity of dynamic cellular membranes . In this context, lack of Annexin A2 expression may have disorganized the actin cytoskeleton which allowed higher parasite multiplication in knockout cells compared to the wild-type ones. Accordingly, Mott et al. (2009)  suggested a physical picture in which an intact, stiff, and rapidly remodeling cytoskeleton facilitates early stages of T. cruzi invasion and parasite retention, followed by subsequent softening and disassembly of the cytoskeleton to accommodate intracellular replication of parasites. These results pointed to actin cytoskeleton as a potential target for novel therapies in order to restrain parasite multiplication and disease progression.
ARF-6 regulates membrane trafficking and interactions of actin cytoskeleton with the plasma membrane. It is involved in membrane trafficking during receptor-mediated endocytosis, endosomal recycling and exocytosis of secretory granules. It is also implicated in the formation of actin-rich membrane protrusions and ruffles. Trafficking of rafts seems to be a major regulatory pathway by which ARF-6 controls Rac1 activation and cell spreading. Induction of PIP2-enriched ruffles and PIP2-positive actin-coated vacuoles by ARF-6 leads to a concomitant accumulation of the annexin 2-p11(S100A10) complex . In this sense, we speculate that during EA-host cell interaction Annexin A2 and ARF-6 may act in a convergent manner.
In summary, our findings demonstrated that ARF-6 and Annexin A2 are involved in the invasion of mammalian cells by T. cruzi amastigotes. Also, ARF-6 was recruited to the amastigote-containing parasitophorous vacuole-containing amastigote. We postulated that ARF-6 and Annexin A2 participate in the reorganization of the actin cytoskeleton during amastigote cell invasion but the exact mechanism remains to be elucidated.
This study was supported by grants and fellowships from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Process: 23038.005295/2011-40) and Fundação de Amparo à Pesquisa do Estado de Minas Gerais (Processes: APQ-00305-12; APQ-00913-13).
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