Biology of Cell Interactions - CNRS URA 2582  


  HEADPr. DAUTRY-VARSAT Alice / adautry@pasteur.fr
  MEMBERSGaëlle Boncompain / Annick Dujeancourt / Rita Furtado / Dr Franck Gesbert / Christiane Goisnard /Alexandre Grassart / Pr Paul Lazarow / Valérie Malardé / Dr Pavel Montes / Dr Meghan Pennini / Stéphanie Perrinet / Dr Nathalie Sauvonnet / Dr Agathe Subtil


  Annual Report

The research of this unit focuses on (i) the mechanisms of entry, signaling and the intracellular fate of receptors (ii) the mechanisms of entry and development of the intracellular bacterium, Chlamydia.

Receptor dynamics and intracellular traffic

Membrane receptors bind their ligands, are endocytosed, and sorted towards degradation or recycling. Endocytosis modulates the expression of membrane components and their signaling activity.

Endocytosis pathways

Receptor-mediated endocytosis through clathrin-coated pits has been by far the most thoroughly investigated. However, other internalization pathways exist, and we have shown that two members of the type I cytokine receptor family, the interleukin-2 receptor β and the common cytokine receptor γc, are internalized by a clathrin-independent pathway. We are investigating the molecular machinery underlying this process. Recent results show that the GTPases RhoA, Rac1 and dynamin are required for this pathway, as well as partners of these factors, the kinases Pak1, Pak2 and cortactin, thereby providing cross-talk between endocytosis, signal transduction and the actin network.

Regulation of IL-2R sorting and intracellular fate

Ectodomain shedding, as well as intracellular degradation, are crucial mechanisms that regulate cell surface receptor turnover. Ubiquitination has been shown to be important for receptor internalisation and sorting. We have demonstrated that cytokine receptors, interleukin-2 receptor β and γc are ubiquitinated, and their cell surface expression is regulated by a ubiquitination/de-ubiquitination machinery, namely by the couple of enzymes c-Cbl/DUB2. We have recently shown that IL-2Rβ undergoes a proteolytic cleavage, generating an intracellular fragment that remains associated with signaling molecules. The physiological function of this fragment as well as the identification of new partners of the IL-2R are under investigation.

Interactions between Chlamydia and the host

Chlamydiae species pathogenic to humans, mainly Chlamydia trachomatis and Chlamydia pneumoniae, cause a number of diseases, including trachoma, pelvic inflammatory disease and pneumonia. We analyze the mechanisms used by the bacteria to enter cells and to sustain their growth.

Identification of type III secreted proteins and functional studies

Throughout their cycle in the host cell, chlamydiae remain in a membrane-bound compartment called an inclusion. Both the bacteria and the host cell contribute to the lipid and protein composition of the inclusion membrane. We have shown that chlamydiae use a type III secretion mechanism to deliver proteins into this membrane and into the cell cytosol. We have identified about thirty proteins that are secreted by this mechanism. These proteins are very likely to be important in Chlamydia pathogenicity and most of our research is dedicated to understanding their function during infection. Some recent work has focused on the interactions between bacterial proteins anchored in the inclusion membrane and host proteins specialized in membrane compartment recognition and fusion, the SNARE proteins. We have shown that some inclusion proteins possess SNARE domains that interact with SNARE proteins of the host, recruiting several intracellular compartments to the inclusion membrane. This study demonstrates for the first time mimicry of the SNARE domain by a bacterium

Keywords: endocytosis, membrane receptor, Chlamydia, intracellular pathogen

Ubic.jpg

Chlamydia infected cell. Bacteria (yellow) develop in a membrane-bound compartment, next to the cell nucleus (blue). We have identified proteins secreted by the bacteria into the cell cytosol (red)



  Publications

Sauvonnet, N., A. Dujeancourt, and A. Dautry-Varsat. 2005. Cortactin and dynamin are required for the clatrin-independent endocytosis of gc cytokine receptor. J. Cell Biol. 168:155-163.

Subtil, A., C. Delevoye, M. E. Balana, L. Tastevin, S. Perrinet, and A. Dautry-Varsat. 2005. A directed screen for chlamydial proteins secreted by a type III mechanism identifies a translocated protein and numerous other new candidates. Mol. Microbiol. 56:1636-1647.

Thoulouze, M. I., N. Sol-Foulon, F. Blanchet, A. Dautry-Varsat, O. Schwartz, and A. Alcover. 2006. Human immunodeficiency virus type-1 infection impairs the formation of the immunological synapse. Immunity 24:547-561.

Wyplosz, B., G. Montalescot, A. Subtil, A. Dujeancourt, M.-L. Tanguy, R. Choussat, L. Capron, and A. Dautry-Varsat. 2006. Correlation between Chlamydia pneumoniae detection from coronary angioplasty balloons and atherosclerosis severity. J.A.C.C. 47:1229-1231.

Derré, I. , Pypaert , M. , Dautry-Varsat, A. and H.Agaisse. 2007. RNAi screen in Drosophila cells reveals the involvement of the Tom complex in Chlamydia infection. PLoS Path. 3:e155.



  Web Site

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Activity Reports 2007 - Institut Pasteur
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